Methods for identifying parkinson's disease therapeutics

Abstract

The present invention features methods of identifying candidate compounds for treating and preventing neurodegenerative disorders such as Parkinson's disease.

Description

FIELD OF THE INVENTION

The field of the invention relates to the treatment of neurodegenerative diseases.

BACKGROUND OF THE INVENTION

Parkinson's disease (PD) is a progressive neurodegenerative disease characterized clinically by bradykinesia, rigidity, and resting tremor. The motor abnormalities are associated with a specific loss of dopaminergic neurons in the substantia nigra pars compacta (SNc) and depletion of striatal dopamine (DA) levels. While the loss of striatal DA correlates with the severity of clinical disability, clinical manifestations of PD are not apparent until about 80-85% of SNc neurons have degenerated and striatal DA levels are depleted by about 60-80%. DA neurons in the ventral midbrain consist of two main groups: the A9 group in the SN, and the A10 group in the medial and ventral tegmentum. Each of these cell groups projects to different anatomical structures and is involved in distinct functions. A9 cells mainly project to the dorsolateral striatum, involved in the control of motor functions, whereas A10 cells provide connections to the ventromedial striatum, limbic and cortical regions, involved in reward and emotional behavior. In addition to the distinct axonal projections and differences in synaptic connectivity, these groups of DA cells exhibit differences in neurochemistry and electrophysiological properties, illustrating functional differences despite similar neurotransmitter identity. These differences in A9 and A10 cells are also reflected in their specific responses to neurodegeneration in PD. Postmortem analyses in human PD brains demonstrate a selective cell loss of the A9 group with a survival rate of about 10% whereas the A10 group is largely spared with a survival rate of about 60%. This indicates that A9 cells are more vulnerable to intrinsic and/or extrinsic factors causing degeneration in PD. In addition, three regional gradients of neurodegeneration in the dorso-ventral/rostro-caudal/medio-lateral axis have been reported in PD. Caudally and laterally located ventral DA cells within A9 subgroups are the most vulnerable cells in PD. In contrast, the medial and rostral part of DA cell subgroups within A10 cells (i.e. rostral, linear nucleus, RLi) are the least affected (5-25% cell loss).

Currently, little is known about the mechanism underlying the neurodegenerative process and the basis for its differential effects on the A9 versus the A10 dopaminergic neurons. Accordingly, disease management is largely limited to strategies that achieve symptomatic relief (e.g., by replenishing dopamine levels) rather than strategies that seek to prevent or delay neurodegeneration. Thus, better treatment methods are needed for treating and preventing neurodegenerative disorders.

SUMMARY OF THE INVENTION

The present invention features methods of identifying compounds useful for the treatment and prevention of Parkinson's disease (PD). The invention is based on our discovery of numerous genes that are differentially expressed in A9 dopaminergic neurons, which undergo a disproportionately high level of cell death in PD, compared to A10 dopaminergic neurons, which are relatively spared. Compounds that reduce or prevent neurodegeneration caused by PD can be identified using screening methods that employ the genes and/or polypeptides that are differentially expressed in neurodegeneration-sensitive (A9) and neurodegeneration-resistant (A10) cells. Screening methods that make use of a plurality of such genes and polypeptides allow for the identification of agents associated with an improved ability to specifically and effectively treat and prevent neurodegeneration.

In one aspect, the invention features a method of identifying a compound that treats or prevents Parkinson's disease in a human, involving the steps of: (a) providing cells that express at least five genes selected from Table 4; (b) contacting the cells with a candidate compound; and (c) assessing the expression level of the genes relative to the expression level of the genes in the absence of said candidate compound, wherein a candidate compound that reduces the expression of at least three of the genes is identified as a compound useful for treating or preventing Parkinson's disease.

In another aspect, the invention features a method of identifying a compound that treats or prevents Parkinson's disease in a human, involving the steps of: (a) providing cells that express at least five genes selected from Table 5; (b) contacting the cells with a candidate compound; and (c) assessing the expression level of the genes relative to the expression level of the genes in the absence of the candidate compound, wherein a candidate compound that increases the expression of at least three of the genes is identified as a compound useful for treating or preventing Parkinson's disease.

In particularly useful embodiments of these screening methods, at least 10, 20, 30, 50, 70, 100, 125, 150, or 200 genes are expressed by the cells and assessed for the level of expression.

In either of the foregoing screening methods, the genes selected from Table 4 and/or 5 may be expressed in a single cell type or in multiple cell types. For assays in which the selected genes are expressed in multiple cell types, the cell types may be mixed in a single heterogeneous culture or they may be segregated from the other cell types (i.e., a homogenous culture). Optionally, some or all of the cells may recombinantly express one or more of the selected genes. Thus, one test system might employ one cell line that naturally expresses one of the selected genes, one cell line transfected with two of the selected genes, and two additional cell lines, each of which is transfected with one of the selected genes. Many other variations of the system are possible such as using five or more cell lines, each of which is transfected with one of the selected genes.

Any mammalian cell type may be used in the foregoing methods. Human cells, rodent (e.g., rat and mouse) cells, and non-human primate cells are particularly useful. The cells may be cultured primary cells (e.g., cultured embryonic ventral mesencephalon cells) or immortalized cells. Useful immortalized cells include, for example, PC12 cells. Desirably, the PC12 cells recombinantly express α-synuclein.

Optionally, the cells may be further treated with a compound that induces cell death (e.g., necrotic death or apoptosis). Such compounds are desirably mitochondrial complex I inhibitors including, for example, 1-methyl-4-phenylpyridinium (MPP⁺), rotenone, isoquinoline, tetrahydroisoquinoline, or 6-hydroxydopamine.

Any method for assessing gene expression is useful in the foregoing methods. For example, the level of gene expression may be assessed by measuring the RNA levels transcribed from the selected genes using techniques such as Northern blotting and/or RT-PCR. Alternatively, the amount of protein expressed by the selected genes may be measured, for example, by Western blotting, ELISA, or measuring the biological activity of protein.

The invention also provides a method of identifying a compound for treating or preventing Parkinson's disease involving the steps of: (a) providing a cell having a reporter gene operably linked to the promoter of a gene selected from Table 4; (b) contacting the cell with a candidate compound; and (c) assessing the level of expression of the reporter gene relative to the level of expression of the reporter gene in the absence of the candidate compound, wherein a candidate compound that reduces the level of expression of the reporter gene is identified as a compound that is useful for the treatment or prevention of Parkinson's disease.

The invention also provides a method of identifying a compound for treating or preventing Parkinson's disease involving the steps of: (a) providing a cell having a reporter gene operably linked to the promoter of a gene selected from Table 5; (b) contacting the cell with a candidate compound; and (c) assessing the level of expression of the reporter gene relative to the level of expression of the reporter gene in the absence of the candidate compound, wherein a candidate compound that increases the level of expression of the reporter gene is identified as a compound that is useful for the treatment or prevention of Parkinson's disease.

Any suitable reporter gene may be used in either of the two foregoing methods. Particularly useful reporter genes include, for example, glucuronidase (GUS), luciferase, chloramphenicol transacetylase (CAT), green fluorescent protein (GFP), alkaline phosphatase, and β-galactosidase. Optionally, the cells may be further contacted with a mitochondrial complex I inhibitor.

Any mammalian cell type is suitable for use in these reporter gene assays. Human cells, rodent (e.g., rat and mouse) cells, and non-human primate cells are particularly useful. The cells may be immortalized cells or they may derived from cultured primary cells (e.g., cultured embryonic ventral mesencephalon cells). Useful immortalized cells include, for example, PC12 cells. Desirably, the PC12 cells also recombinantly express α-synuclein.

The invention also features a solid support surface (e.g., multiwell plate or slide) containing 1000 or fewer unique polynucleotide probes capable of binding at least 200 distinct nucleic acids that encode genes contained in Table 4 and Table 5, wherein the probes are arranged on the surface such that, when contacted with a sample containing said nucleic acids, each binding event is segregated from the others.

In preferred embodiments, the polynucleotide probes are capable of binding at least 300 or at least 400 distinct nucleic acids that encode genes contained in Table 4 and Table 5. Desirably, the polynucleotide probes are conjugated to a detectable label such as a fluorescent label or an enzyme tag. Useful labels include, for example, digoxigenin, β-galactosidase, urease, alkaline phosphatase, peroxidase, or an avidinibiotin complex.

By a “promoter” is meant a nucleic acid sequence sufficient to direct transcription. Also included in the invention are those promoter elements which are sufficient to render promoter-dependent gene expression controllable for cell type-specific, tissue-specific or inducible by external signals or agents; such elements are usually located in the 5′ region of the native gene, but may also be found in the 3′ regions.

By “operably linked” is meant that a nucleic acid molecule and one or more regulatory sequences (e.g., a promoter) are connected in such a way as to permit expression of the gene product (i.e., RNA) when the appropriate molecules (e.g., transcriptional activator proteins) are bound to the regulatory sequences.

By a “mitochondrial complex I inhibitor” is meant any compound that reduces the activity of the mitochondrial respiratory chain complex thereby reducing the oxidative phosphorylation and/or increasing production of mitochondrial reactive oxygen species. The reactive oxygen species may in turn result in the induction of apoptosis. Exemplary mitochondrial complex I inhibitors are 1-methyl-4-phenylpyridinium (MPP⁺), rotenone, isoquinoline, and tetrahydroisoquinoline.

By “specifically binds,” when referring to an interaction between distinct molecules such as polynucleotides, is meant a binding event for which the target molecule and the receptor molecule (e.g., probe) interact with high affinity and specificity. The receptor molecule does not substantially bind to any other non-target molecules that are present. Preferably, the specific binding contributes 75%, 85%, 90%, 95%, 99%, or 100% of the total binding detected in the sample.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1A is a tyrosine hydroxylase (TH)-immunostain of the coronal section of the mouse midbrain. A9 dopaminergic neurons are located in the substantia nigra pars lateralis (SNl) and the substantia nigra pars compacta (SNc). A10 dopaminergic neurons are located in the ventral tegmental area (VTA), the nucleus paranigralis (PN), and the interfascicular nucleus (IF).

FIGS. 1B-1D are TH-immunostains showing brain sections that were used in the laser capture microscopy (LCM) procedure. FIG. 1B shows TH-positive neurons in the SNc before laser capture. In FIG. 1C, TH-positive cells were targeted for laser capture using a 7.5 μm diameter-laser. Captured cells on the thermoplastic film were visualized before processing for RNA extraction (FIG. 1D).

FIG. 1E is a bar graph showing GIRK2 and calbindin mRNA levels in LCM samples, as measured by real time PCR. GIRK2 was increased by 2.78 fold (SEM±0.95) in A9 cells and calbindin was increased by 2.90 fold (SEM±0.64) in A10 cells.

FIGS. 1F-1H are bar graphs showing the functional profiles of microarray data. Genes that were induced in A9 and A10 cells were categorized based on their biological functions and cellular components by Onto-Express. Genes associated with a fold induction of greater than 1.5 (FDR<5%) were distributed into different categories, such as metabolism (FIG. 1F), cellular component in cytoplasm (FIG. 1G), transport, and signal transduction mechanism (FIG. 1H).

FIGS. 2A and 2B show a series of pictures of PC12-α-Synuclein (Syn)-overexpressing GIRK2 cells. Cells were infected with an eGFP or GIRK2-expressing lentivirus at an MOI of 5. Higher GIRK2 expression was achieved in GIRK2-infected cells relative to eGFP-infected control cells. Red staining represents GIRK2 and cell nuclei was visualized by DAPI staining (blue).

FIG. 2C is a bar graph showing cell death induced by MPP⁺ toxicity (1 and 5 mM) in PC12-αSyn cells, as measured by LDH release. LDH release was significantly increased in GIRK2-overexpressing cells compared to control eGFP-overexpressing cells (*; p<0.05 between groups).

FIG. 2D is a bar graph showing cell death induced by MPP⁺ toxicity in PC12-αLSyn, as measured by LDH release. LDH release was significantly reduced by FGF1 treatment (*; p<0.05 between groups). A Student's t-test was used to obtain statistical significance.

FIGS. 3A-3E are bar graphs showing cell death induced by MPP⁺ toxicity in PC12-αSyn. These graphs demonstrate the neuroprotective effects that results from increasing concentrations of NT-3 and several neuropeptides. Cells were pretreated with NT-3, VIP, CGRP, CCK-8, or GRP for two hours prior to 1 mM MPP⁺ treatment for 24 hours. The levels of LDH release were presented as a percent of control group without treatment. Significant dose-dependent reductions in LDH release were detected in these experiments indicating neuroprotective effects of these peptides from toxic insult (*; p<0.01 in the comparison with the group of MPP⁺ only treatment).

FIG. 4A is a series of immunostains of primary VM cells. Immunostaining of primary VM culture show TH-positive (left), GIRK2-positive (middle), and TH-positive/GIRK2-positive cells (right).

FIG. 4B is a bar graph representing the number of dopaminergic neurons as a at various MPP⁺ concentrations. TH-positive/GIRK2-positive or TH-positive/GIRK2-negative cells were stereologically counted following MPP⁺ treatment and were presented as % of total TH-positive neurons of control conditions. TH-positive/GIRK2-positive cells were more vulnerable to MPP⁺ than TH-positive/GIRK2-negative cells (*; p<0.05 in the comparison with the control condition).

FIG. 4C is a bar graph showing the number of GIRK2-positive dopaminergic neurons. GRP was added to a primary VM culture at day 5, two hours prior to treatment with MPP⁺ (10 μM). After 48 hours, TH-positive/GIRK2-positive neurons were stereologically counted as A9-like dopaminergic neurons and presented as % of total TH-positive/GIRK2-positive neurons of control (no MPP⁺) conditions (*; p<0.05 in the comparison with the group of MPP⁺ only treatment (black bar graph)). A Student's t-test was used to obtain statistical significance.

FIGS. 5A-5C are graphs showing differential gene expression between A9 and A10 cells. All genes were plotted on a log scale and represent a comparison between samples of A9- and A10-microdissected samples. Five A9 replicates are plotted against six A10 replicates to determine the differential gene expression between these groups. The distance from the mid-line reflects increasing levels of differential gene expression. All data were normalized using the probe level Robust Multi-Chip Analysis (RMA) algorithm.

FIGS. 6A-6D is series of photomicrographs of TH/GIRK2-immunostained E14 primary cell cultures. Scale bar in FIGS. 6A-6C=50 μm. Scale bar in FIGS. 6D=10 μm.

FIGS. 6E-6G are photomicrographs of immunostained E14 primary cell cultures. The effect of NT3 on survival of TH (green) and TH/GIRK2 (yellow) double-labeled neurons in primary VMDA culture is shown. NT3 at 17 ng/ml protects the cells against MPP⁺ toxicity (3 mM). Scale bar=100 μm.

FIGS. 7A-7C are photomicrographs of immunostained E14 primary cell cultures demonstrating the neuroprotective effect of VIP in primary VM culture. Immunostaining against TH (green) and GIRK2 (red) was performed 48 hours after 10 μM of MPP⁺ was applied to VM culture in the absence or presence of 10⁻⁶ M VIP.

FIG. 8 shows a series of graphs representing cell death in DAN cells, as measured by LDH release. MPP⁺ administration provides a toxic insult to DAN cells, which is maximal at a dose of 2.5 mM. NT-3 is neuroprotective since cells pretreated with NT-3 for two hours prior to MPP⁺ treatment (1 mM) show a significant dose-dependent reduction in LDH release.

FIGS. 9A-9I are photomicrographs of tyrosine hydroxylase (TH) immunohistochemistry of the ipsilateral striatum following intrastriatal 6-OHDA administration. The time course following 6-OHDA administration is: FIG. 9A=control; FIG. 9B=3 days; FIG. 9C=5 days; FIG. 9D=10 days; FIG. 9E=21 days; and FIG. 9F=28 days. Striatal TH fiber loss and nigral TH cell loss is seen in 6-OHDA lesioned rats. These immunostains show the conversion of the normal innervation of the contralateral side of the lesion to a fully denervated striatum 28 days after 6-OHDA striatal lesion. FIGS. 9G-9I are photomicrographs of tyrosine hydroxylase (TH) immunohistochemistry of the substania nigra 0, 10, and 28 days after intrastriatal 6-OHDA administration, respectively. There is a progressive loss of dopaminergic neurons on the lesioned side at 10 and 28 days compared to the unlesioned side.

FIGS. 10A and 10B are bar graphs quantifying the progressive loss of dopaminergic neurons in the substantia nigra of 6-OHDA lesion model rats. At post-lesion day 21, the continued loss of the TH positive cells can be prevented by delivering neurotrophic and neuroprotective molecules or genes.

FIG. 11 is a series of photomicrographs from experiments using eGFP lentiviral expression vector. PC12 and primary ventral mesencephalic dopaminergic (VMDA) neurons were transduced with an eGFP-expressing lentivirus at an MOI of 5 and 3, respectively. Four days after transduction, cells were stained with Rhodamine Red-labeled α-synuclein (PC12) or TH-specific (primary VMDA cell cultures) antibodies and analyzed using a confocal microscope (upper two rows). One hundred percent transduction efficiency was observed for PC12 cells and TH-expressing primary neurons. For in vivo transduction, SN of rats was injected with 10⁶ to 2×10⁶ TU of the lentivirus and eGFP expression was analyzed by fluorescence microscopy 6 days after injection. An exemplary virus-transduced SN stained with an anti-TH antibody is shown in the lower two rows. The majority of the midbrain TH-positive neurons were transduced with the eGFP-expressing lentivirus (yellow cells marked by arrows in high magnification).

DETAILED DESCRIPTION

In order to understand the innate physiological differences between A9 and A10 neurons for the purpose of identifying novel therapies and therapeutic targets, and developing drug screening and diagnostic assays for Parkinson's disease (PD), individual A9 and A10 dopaminergic neurons were isolated by laser capture microdissection (LCM) and genomic profiles assessed by microarray analysis. The results show differential gene expression in A9 and A10 which may contribute to their altered vulnerability in PD. Further, differential expression of selected proteins in in vitro dopaminergic cells (e.g., α-synuclein-overexpressing PC12 cells (PC12-α-syn) and primary ventral mesencephalic (VM) cultures) alters the cells' sensitivity to MPP⁺ toxicity. Several of the polypeptides identified by microarray analysis were also differentially expressed within reported Parkinson's disease linkage intervals. Accordingly, proteins that are preferentially expressed in A10 cells (Table 5) may increase the cellular threshold to the neurodegenerative process in Parkinson's disease; whereas, proteins preferentially expressed in A9 cells (Table 4) may be responsible for their susceptibility to degeneration in Parkinson's disease.

Differential Expression Between A9 and A10 Dopaminergic Neurons

Midbrain A9 and A10 DA neuronal groups were identified by rapid TH-immunostaining to minimize RNA degradation in tissue sections and were next microdissected by laser-capture microscopy using anatomical criteria (FIGS. 1A-D). The quality of the extracted RNA samples was validated by real time PCR of G-protein coupled inward rectifying potassium channel isoform 2 (GIRK2), a molecule known to be more expressed in A9 DA neurons, and calbindin, a molecule known to be more expressed in A10 DA neurons (FIG. 1E).

Microarray analysis was performed to investigate the molecular differences between dopaminergic neurons located in the A9 and A10 midbrain regions. Five biological replicates from A9 regions and six biological replicates from A10 regions of mouse brain were analyzed on an Affymetrix Murine 430A high-density oligonucleotide array, which currently queries 20,000 murine probe sets. Paired hybridization results between replicates of A9 (FIG. 5A) and A10 (FIG. 5B) samples demonstrated the reproducibility between the biological replicates. The distribution of gene expression signal from the combined data of the A9 and A10 series displayed the similarity and even distribution of up-and down-regulated genes in the plot (FIG. 5C). The differences that distinguished these two neuronal populations illustrated that only a small number of genes were differentially expressed. Forty-six genes had greater than 2.0-fold elevation of mRNA levels in A9 compared to A10 DA neurons, and 199 genes, greater than 1.5-fold (false discovery rate [FDR]<5%). Sixty-one genes had greater than 2.0-fold elevation of mRNA level in A10 compared to A9 DA neurons and 163 genes, greater than 1.5 fold (FDR<5%) (Tables 4 and 5).

The microarray analysis was validated in two ways. Firstly, previously reported gene expression differences between A9 and A10 DA neurons were verified. For example, Raldh1 was more expressed in A9, and calbindin D28K and cholecystokinin more in A10 DA neurons (Tables 4 and 5). Secondly, using real time PCR of laser-captured RNA samples, the mRNA levels of several genes from our microarray analysis was quantified to confirm A9/A10 gene expression patterns (Table 1). From various functional pathways, genes with relatively high mRNA expression and/or potential biological association to relative vulnerability were selected for validation.

TABLE 1
Relative Overexpression of Selected Genes in Midbrain DA Neurons
				Fold
	Category	Accession	Gene	change
A9	Growth factor	NM_010197	Fibroblast growth factor 1	4.7 ± 0.4
		NM_010512	Insulin-like growth factor 1	2.5 ± 0.1
		NM_008010	Fibroblast growth factor receptor 3	3.7 ± 1.3
	Mitochondrial protein	NM_007451	Adenine nucleotide translocator 2	2.4 ± 0.4
	Energy metabolism	NM_008492	Lactate dehydrogenase 2, B chain	2.6 ± 0.5
	Vesicle mediated	NM_026697	RAB14	2.2 ± 0.2
	transport
	Enzyme-linked	NM_011219	Protein tyrosine phosphatase	2.3 ± 0.4
	receptor/phosphatase		z-polypeptide 1
	Apoptosis	NM_007611	Caspase 7	2.6 ± 1.1
	Cell surface	NM_009846	CD24a	5.6 ± 0.9
	marker
A10	Neuropeptide	NM_013732	Cocaine and amphetamine regulated	4.7 ± 0.3
			transcript
		NM_011702	Vasoactive intestinal polypeptide	4.4 ± 1.5
		NM_175012	Gastrin releasing peptide	8.5 ± 2.0
	Calcium binding	NM_009037	Reticulocalbin	4.3 ± 0.1
	protein	NM_009788	Calbindin D28K	2.9 ± 0.6
	Lipid metabolism	NM_008509	Lipoprotein lipase	5.3 ± 1.7
	Phosphatase inhibitor	NM_011153	G-substrate	2.9 ± 1.0

To gain insight into the biological relevance of differential A9/A10 gene expression, genes exhibiting differences greater than 1.5 fold (FDR<5%) were analyzed with Onto-Express (OE) software, which systematically translates genetic input into functional profiles. Genes from several categories showed striking differences between cell groups. Genes related to metabolism (FIG. 1F) and genes encoding mitochondrial proteins (FIG. 1G) were more expressed in A9 DA neurons compared to A10 DA neurons. Genes involved in protein, lipid and vesicle-mediated transport, but not ion transport, were also found to be more highly expressed in A9 DA neurons (FIG. 1H). In addition, among a number of genes involved in signal transduction mechanisms, enzyme-linked receptor genes such as receptor tyrosine kinases and receptor tyrosine phosphatases were more expressed in A9 DA neurons (FIG. 1H); whereas, all of the signal transduction genes with elevated expression in A10 fell into the category of G-protein coupled receptors. Notably, several genes related to small GTPase-mediated signaling and synaptic vesicle recycling, including RAB and RAS proteins, were more expressed in A9 DA neurons (FIG. 1H) and genes related to neuropeptide and hormone activity were typically elevated in A10 cells (Table 2).

TABLE 2
Differential Expression of Selected Genes in Neuronal Subpopulations
	A9	A10
Neuropeptide/	Secreted phosphoprotein 1	Cocaine and amphetamine regulated
hormone	Neueopeptide Y receptor Y5	transcript
activity	Neurotensin receptor 2	Calcitonin/calcitonin-related
		polypeptide, alpha
		Colony stimulating factor 2 receptor,
		beta 2
		Growth hormone receptor
		Gastrin releasing peptide
		Vasoactive intestinal polypeptide
		Tachykinin receptor 3
		Adenylate cyclase activating
		polypeptide 1
		Cholecystokinin
		Arginine vasopressin receptor 1A
Growth factor	Fibroblast growth factor 1
activity	Fibroblast growth factor receptor 3
	Fibroblast growth factor inducible 15
	Insulin-like growth factor 1
	Epidermal growth factor pathway
	substrate 8
Protease	Caspase 7
	Protease, serine, 11 (Igf binding)
Protease		Plexin C1
inhibitor		Cysteine-rich motor neuron 1
		Serine protease inhibitor, Kunitz
		type2
Phosphatase	Protein tyrosine phosphatase z
	polypeptide 1
	Protein phosphatase 2A, regulatory
	subunit B (B56)
Phosphatase		G-substrate
inhibitor
Apoptosis	Caspase 7	Pleomorphic adenoma gene-like 1
	Bcl-2 like 11 (apoptosis facilitator)	Mitogen activated protein kinase
	Estrogen-related receptor β like 1	kinase kinase 5
	Programmed cell death 10

Certain opposing molecular functional categories exhibit inverse expression patterns in A9 and A10 DA neurons. For example, gene expression of proteases and phosphatases are elevated in A9 DA neurons; whereas, inhibitors of proteases and phosphatases were more highly expressed in A10 DA neurons (Table 2). Two pro-apoptotic genes, caspase 7 and Bcl2-like 11, are more highly expressed in A9 cells (Table 2).

The microarray data was further analyzed by comparing the genomic profiles with candidate susceptibility genes for PD generated by previous genomic convergence analysis that combined a genomic linkage and expression analysis (Hauser et al., Hum. Mol. Genet. 12: 671-7, 2003). That study reported 402 genes in the human substantia nigra that lay within five large genomic linkage regions identified in 174 PD families. Several differentially expressed genes in A9 and A10 DA neurons from the present microarray analysis were identical or similar to genes within the reported PD linkage intervals (Table 3).

TABLE 3
Concurrence Between Human Genomic Convergence Analysis in PD Families
and Murine Microarray Analysis
	Differentially expressed genes in A9 and A10
Gene located in PD linkage interval from	from Mouse Microarray Analysis
Human Genomic Convergence Analysis		A9/
Unigene	Description	Unigene	Description	A10
Hs.75297	FGF1	Mm.5087	FGF1	A9
Hs.7688	PP2A regulatory subunit B	Mm.3785	PP2A regulatory subunit B	A9
	Beta isoform		Gamma isoform
		Mm.46735	RAB3C	A9
		Mm.1387	RAB11a	A9
		(Mm.14530)	RAB1	A9
		Mm.271944
Hs.5807	RAB14	Mm.198264	RAB14	A9
Hs.301853	RAB34
Hs.479	RAB5C
Hs.55099	RAB6 GTPase activating protein
	(GAP and centrosome associated)
Hs.19012	RAB9 effector p40
Hs.31547	NADH dehydorgenase	Mm.44227	NADH dehydrogenase	A9
	(ubiquinone) 1 alpha subcomplex, 8		(ubiquinone) Fe—S protein 8
Hs.79172	Solute carrier family 25	Mm.658	Solute carrier family 25	A9
	(mitochondrial carrier; adenine		(mitochondrial carrier; adenine
	nucleotide translocator), member 5		nucleotide translocator), member 5
Hs.8262	Lysosomal-associated membrane	Mm.197518	Lysosomal-associated membrane	A9
	protein 2		protein 4B
Hs.90998	Septin6	Mm.2214	Septin4	A9
Hs.37144	MAGUK p55 subfamily member 3	Mm.20449	MAGUK p55 subfamily member 3	A10
Hs.3972	Sialyltransferase 7D	Mm.4954	Sialyltransferase 8B	A10
Hs.82302	Heparin sulfate 6-sulfotransferase 2	Mm.41264	Heparin sulfate 6-sulfotransferase 2	A10

In Vitro Models of Parkinson's Disease

In vitro models, using a wide array of cell types, may be used in the screening methods of this invention to identify candidate compounds for the treatment of PD. These models also may be used to tested the effects of the candidate compounds on cell survival and neurodegeneration. Primary fetal dopaminergic neurons or cell lines exhibiting some characteristics of the dopaminergic neuronal phenotype may be used in the present invention. Cell lines have the advantage of providing a homogeneous cell population, which allows for reproducibility and sufficient number of cells for experiments. Primary dopaminergic cultures are derived from tissues harvested from developing ventral mesencephalon (VM) containing the substantia nigra. They have the advantage of containing authentic dopaminergic neurons cultured in a context of their naturally occurring neighboring cells. In our studies, we also employed human dopaminergic neuron progenitor (DAN) cells, using an isolation technique that produces up to 70% dopaminergic neurons with robust immunoreactivity for dopamine, tyrosine hydroxylase (TH), and dopamine transporter (DAT) following in vitro differentiation. We also employed cell culture models characterized by abnormal protein aggregation and degradation, which are related to the ax-synuclein/ubiquitin-proteasome system (UPS). In these models, the overexpression of wild type α-synuclein causes an impaired mitochondrial respiratory chain function. The overexpression of mutant α-synuclein (A53T and A30P) produces oxidative stress and an impaired function of the UPS, leading to apoptosis (A53T). The inducible expression of mutant α-synuclein (A30P) in PC12 cells reduces proteasome functions and increases mitochondria-dependent apoptosis after sub-threshold toxic concentrations of proteasome inhibitor (lactacystin). Any of these cell culture models are useful for the screening methods of the invention and are described in more detail below.

Tet-Inducible (Tet-Off) α-Synuclein Overexpressing PC12 Cells

A PC12 cell line was transfected to express wild type human α-synuclein using the Tet-Off system (Clontech Laboratories, Palo Alto, Calif.). α-Synuclein expression was suppressed using 1 μg/mL doxycycline (Clontech) in culture media before expression is required. α-Synuclein expressing PC12 cells (PC12-αSyn) were grown in Dulbecco's modified Eagle's medium (DMEM) (Invitrogen, Calsbad, Calif.) supplemented with 10% heat-inactivated horse serum, 5% heat-inactivated fetal calf serum (Hyclone, Logan, Utah), 4 mM L-glutamine, streptomycin, and penicillin G (Fisher, Pittsburgh, Pa.). Cells were maintained at 37° C., in 5% CO₂ humid atmosphere.

The effects of various neuroprotective agents were examined in the PC12-αSyn cell line. To determine MPP⁺ neurotoxicity in α-synuclein- and naïve PC12 cells, cell death was measured by LDH release assays. The PC12-αSyn cells showed a significantly higher LDH release in response to an intermediate concentration (2.5 mM) of MPP⁺ than naive PC12 cells, but there was no significant difference between the two groups when treated with higher concentrations of MPP⁺. This indicated that below a threshold of “toxic overload”, α-synuclein overexpression provided a more susceptible environment to MPP⁺ insult. When the PC12-αSyn cells were pretreated with neuroprotective agents such as BAF, a pan-caspase inhibitor, this MPP⁺ susceptibility was significantly decreased demonstrating that the PC12-αSyn cell model is useful for studying neuroprotection in vitro.

GIRK2 is known to be more expressed in A9 DA neurons and linked to degeneration of A9 DA neurons in the weaver mouse. We tested whether an increase in GIRK2 expression levels can modulate vulnerability to MPP⁺ in PC12-αSyn (FIGS. 2A and 2B). This cell culture model combines two features of PD-related pathogenetic mechanisms: MPP⁺ toxicity and α-synuclein overexpression. Overexpression of α-synuclein increased susceptibility of PC12 cells (PC12-αSyn) to MPP⁺ compared to control PC-12 cells. Lentivirus-mediated overexpression of GIRK2 in PC12-αSyn resulted in significantly increased vulnerability at low (1 mM) and high (5 mM) MPP⁺ concentrations compared to control (eGFP-transduced) cells (FIG. 2C). Thus, GIRK2 is a gene that is naturally overexpressed in the A9 DA neurons and contributes to increased susceptibility to MPP⁺ in the presence of α-synuclein.

To further investigate whether differentially expression proteins contribute to the survival differences between DA neuronal subtypes, other candidates from the comparative genetic profiles (Table 2) were tested. The results in Table 2 demonstrate that growth factor activity, especially FGF-related activity, is prominent in A9 dopaminergic neurons. FGF1 was chosen for further investigation because its mRNA expression level and that of its receptor, FGFR3, are relatively high (Table 1). Additionally, the FGF1 gene is contained in Parkinson's disease linkage region (Table 3). The data in FIG. 2D demonstrate that FGF1 was able to protect PC12-αSyn cells from MPP⁺ in a dose-dependent manner.

A10 DA neurons are less vulnerable in PD. Certain genes more highly expressed in A10 compared to A9 DA neurons may play a neuroprotective role. The neurotrophic factor, NT-3, which is known to have elevated expression in A10 dopaminergic neurons, was tested in the PC12-αSyn assay described above. NT-3 was able to protect PC12-α-Syn cells from MPP⁺ neurotoxicity in a dose-dependent manner (FIG. 3A).

The microarray analysis reveals that a group of neuropeptides is elevated in A10 dopaminergic neurons (Tables 1 and 2). Because neuropeptides are known to exert trophic effects, several were chosen to test their potential protective effects from MPP⁺ toxicity in PC12-αSyn cells. Vasoactive intestinal peptide (VIP), calcitonin/calcitonin gene-related peptide alpha (CGRP), cholecysokinin-8 (CCK-8), and gastrin releasing peptide (GRP) were individually applied to the test cells in the presence of 1 mM MPP⁺. All of these neuropeptides exhibited dose-dependent neuroprotective effects as determined by LDH assay (p<0.01; FIGS. 3B-3E).

Primary Ventral Mesencephalic Dopaminergic Neuronal (VMDA) Cell Culture

Primary cultured VMDA cells contain a mixed cell population of A9-like and A10-like DA neurons and can be used in the screening methods of the invention. These cultures have several advantages including providing authentic DA neurons cultured with their naturally occurring neighboring cells.

VMDA cultures were obtained from E15 Sprague-Dawley rat (Charles River, Mass.) ventral mesencephalon (VM). Tissue was mechanically dissociated with a pasteur pipette. The cells were resuspended in DMEM containing heat-inhibited horse serum (10%), glucose (6.0 mg/ml), penicillin, streptomycin, and 2 mM glutamine (Gibco). Cell suspensions containing 4×10⁵ cells were plated on a coverslip in a 24-well plate, precoated with a 1:500 diluted solution of polyornithine and fibronectin in 50 mM sodium borate (pH 7.4) overnight.

Primary ventral mesencephalic (VM) cultures were used to further delineate the protective effects of neuropeptides on dopaminergic neurons. These cultures contained a mixed cell population having approximately 40% of TH-positive neurons at 5 days in vitro (DIV) with both A9- and A10-like dopaminergic neurons (FIG. 4A). GIRK2-positive cells were more vulnerable to MPP⁺ compared to GIRK2-negative cells (FIG. 4B). The cultures were treated with MPP⁺ at day 5 for 48 hours using concentrations ranging from 0.1 to 10 μM. Cells were fixed with paraformaldehyde for immunostaining of TH and GIRK2 48 hours after MPP⁺ treatment. These results further demonstrate that increased vulnerability of neurons that express high levels of GIRK2.

The neuroprotective effect of GRP, NT-3 and VIP was examined in these primary VM cell cultures. Each of the polypeptide factors, GRP (FIG. 4C), NT-3 (FIGS. 6A-6G), and VIP (FIGS. 8A-8C) exhibited a significant protective effect against MPP⁺ toxicity GIRK2-positive/TH-positive neurons. The cultures were pretreated with the polypeptide factors 2 hours prior to 10 μM MPP⁺ treatment.

We have determined the conditions of MPP⁺ toxicity in the VM cultures and demonstrate neuroprotective effects of neuropeptides typically more abundantly expressed by A10 DA neurons, when added to the culture medium (FIGS. 4, 6A-6G, and 7A-7C). These data show that VM cultures are a useful tool for testing neuroprotection as described herein.

Human Dopaminergic Neuron Precursor (DAN) Cells

DAN cells, which have been used to study neurodegeneration, can be used in the methods of this invention; they express multiple genes of Tables 4 and/or 5, and the expression of these genes following contact with a candidate compound can be measured. DAN cells exhibit the neurochemical characteristics of mesencephalic DA neurons, e.g. greater than 70% of DAN cells have robust immunoreactivity for dopamine, TH, DAT and vesicular monoamine transporter (VMAT) and more than 90% of DAN cells are neurons. DAN cells are sensitive to the neurotoxin MPP⁺. NT3, one of our candidate molecules from our microarray data, was shown to have a protective effect in MPP⁺ treated DAN cells, decreasing cell death as detected by lactate dehydrogenase (LDH) release assays (FIG. 8). These data suggest that our DAN cell system is appropriate to study the europrotection/vulnerability of our candidate molecules.

In Vivo Models of Parkinson's Disease

Several in vivo models of Parkinson's disease exist that mimic some of the clinical and pathological features of Parkinson's disease including, for example, L-dopa-responsive movement disorder, a chronically progressive loss of dopaminergic neurons, and the presence of Lewy body (LB)-like inclusions. These models can be used to confirm results obtained using the methods of the invention. In these models, the neurotoxins 6-OHDA and MPTP are commonly used to induce dopaminergic neuronal cell death leading to parkinsonism. In rats, intrastriatal 6-OHDA causes progressive degeneration of dopaminergic neurons in SN similar to the slope of the time-course seen in human PD. MPTP also causes selective dopaminergic neuronal loss in brain areas similar to idiopathic PD in mice and primates. In primates, intracarotid administered MPTP is used for a rapid destruction of dopaminergic neurons in the substantia nigra followed by symptoms of parkinsonism. Since this model lacks typical aspects of slowly progessive neurodegeneration, it is limited in modeling the pathophysiology of Parkinson's disease in patients. We have further improved this model by repeated systemic administration of low doses of MPTP to induce a parkinsonian syndrome that shares many characteristics with idiopathic Parkinson's disease. This model is useful for testing the effects of neuroprotective molecules in primates.

Another model for Parkinson's disease is based on the injection of α-synuclein-expressing recombinant Adeno Associated Viruses (rAAV-α-syn) into the striatum of rodents and primates. Since α-synuclein is a major component of LBs, overexpression of wild type or mutant (A53T and A30P) α-synuclein selectively induces an α-synucleinopathy including LB formation in targeted DA neurons.

Progressive 6-OHDA Lesioned Rats

Female Sprague Dawley rats (200-250 g, Charles River, Wilmington, Mass.) receive unilateral intrastriatal stereotaxic injections of 6-OHDA (Sigma, St. Louis, USA) using a 10 μl Hamilton syringe. Intramuscular injections of Acepromazine (3.3 mg/kg, PromAce, Fort Dodge, Iowa) and atropine sulfate (0.2 mg/kg, Phoenix Pharmaceuticals, St. Joseph, Mo.) is given 10 minutes before animals will be anesthetized with ketamine/xylazine (60 mg/kg and 3 mg/kg respectively, i.m.). A concentration of 3.0 μg/μl free base 6-OHDA dissolved in 0.2% ascorbic acid/saline (Sigma) is injected into 3 locations (2.5 μl/site, total dose 22.5 μg) in the right striatum at the following coordinates (calculated from bregma): site 1, AP+1.3, L−2.8, DV−4.5, IB−2.3; site 2, AP+0.2, L−3.0, DV−5.0, IB−2.3; site 3, AP−0.6, L−4.0, DV−5.5, IB−2.3 mm. FIGS. 9A-9F shows the progressive time course of dopaminergic fiber loss in the striatum of 6-OHDA-lesioned rats. The loss of striatal dopaminergic fibers is accompanied by a progressive degeneration of dopaminergic neuronal cell bodies in the substantia niga (FIGS. 9G-I). These results are quantified in FIGS. 10A-10B.

Behavioral Test for Rat Models

Behavioral bioassays of the DA system may be used as follows. For the head bias assessment, the animals are placed into observation cages in a quiet room with dim lighting and allowed to habituate for 5 minutes. For one minute, the animals are scored according to exhibited head bias to one side or the other during each second if the animals' heads may be 10° or more out of line with their shoulders in either direction. The seconds are monitored with a digital metronome. Each animal will be scored three times, all of which occurred after a single habituation period. The scores are then summed between periods, and the percentage of bias to the contralateral side is calculated and reported as the final score.

For the cylinder test, the animals is placed inside an 18-gallon cylinder (Nalgene, Rochester, N.Y.) between two mirrors set up at right angles to each other to facilitate scoring of movements made on sides of the cylinder not facing the observer. The rats are videotaped for the 3 minutes immediately following placement. After the test, an observer scores each instance in which a rat beginning with all four paws on the floor places one or both forelimbs on the wall of the cylinder. The score is recorded as the fraction of total contacts in which the paw contralateral to the lesion touched the wall first.

For the apomorphine assessment, the animals receive 0.1 mg/kg subcutaneous injection of apomorphine. The animals are placed in the same recording system as in the amphetamine test, and are monitored for 40 minutes. Follow-up assessments are conducted with the same protocol.

Lesioned animals are selected for study by examination of rotational behavior in response to a 4 mg/kg intraperitoneal (i.p.) injection of amphetamime. The animals are randomized and placed in automated rotometer bowls and left and right full-body turns are monitored via a computerized activity monitor system for 90 minutes. Follow-up amphetamine rotation studies may be conducted following the same protocol.

Identification of Candidate Compounds Useful for Treating Parkinson's Disease

A candidate compound that is beneficial for treating or preventing PD can be identified using the methods of this invention. A candidate compound can be identified for its ability to reduce the expression or biological activity of a gene listed in Table 4 or increase the expression or biological activity of a gene listed in Table 5, or both. Candidate compounds that modulate the expression level or biological activity of the polypeptide of the invention by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 100%, or more relative to an untreated control not contacted with the candidate compound are identified as compounds useful for treating and preventing PD.

Customized High Throughput Expression Screening Systems

Customized “gene chips” provide a high-throughput system for screening large numbers of samples obtained from in vitro or in vivo tissue sources. Genes involved in the pathology of PD are first selected (including those listed in Tables 4 and 5) and a customized gene chip is next created by immobilizing the appropriate nucleic acid probes on a solid support. Selected nucleic acid probes are immobilized onto predetermined regions of a solid support by any suitable techniques that affect a stable association (i.e., the nucleic acids remain localized to the predetermined region under hybridization and washing conditions) of the probes with the surface of a solid support.

The nucleic acids may be covalently associated with or non-covalently attached to the support surface. Examples of non-covalent association include binding as a result of non-specific adsorption, ionic, hydrophobic, or hydrogen bonding interactions. Covalent association involves formation of chemical bond between the nucleic acids and a functional group present on the surface of a support. The functional group may be naturally occurring or introduced as a linker. Non-limiting functional groups include but are not limited to hydroxyl, amine, thiol and amide. Exemplary techniques applicable for covalent immobilization of polynucleotide probes include, but are not limited to, UV cross-linking or other light-directed chemical coupling, and mechanically directed coupling (see, for example, U.S. Pat. Nos. 5,837,832, 5,143,854, 5,800,992, WO 92/10092, WO 93/09668, and WO 97/10365). A preferred method is to link one of the termini of a nucleic acid probe to the support surface via a single covalent bond. Such configuration permits high hybridization efficiencies as the probes have a greater degree of freedom and are available for complex interactions with complementary targets.

A probe may be associated with the surface directly or may be indirectly associated by an intermediate “spacer” moiety. Such a spacer can be of any material, e.g., any of a variety of materials which are conventional in the art. In one embodiment, the spacer is an organic moiety having, e.g., about 5-20 Cs. In another embodiment, the spacer is a nucleic acid (of any of the types describes elsewhere herein) which does not undergo specific interaction or association with, e.g., a target nucleic acid of the invention.

Typically, each array is generated by depositing a plurality of probe samples either manually or more commonly using an automated device, which spots samples onto a number of predefined regions in a serial operation. A variety of automated spotting devices are commonly employed for production of polynucleotide arrays. Such devices include piezo or ink-jet devices, automated micro-pipetters and any of those devices that are commercially available (e.g. Beckman Biomek 2000). The total number of probe samples spotted on the support will vary depending on the number of different polynucleotide probes one wish to display on the surface, as well as the number of control probes, which may be desirable depending on the particular application in which the subject array is to be employed. Generally, the array comprises at least about 20 distinct polynucleotides, usually at least about 100 polynucleotides, preferably about 1000 polynucleotides, more preferably about 10,000 polynucleotides, but will usually not exceed 100,000 polynucleotides, wherein each polynucleotide is complementary to a target nucleic acid. The polynucleotide spots may take a variety of configurations ranging from simple to complex, depending on the intended use of the array. The probes may be spotted in any convenient pattern across or over the surface of the array so as to from a grid, a circular, ellipsoid, oval or some other analogously curved shape. Within a predetermined region, the probes are deposited in an amount sufficient to provided adequate hybridization and detection of target nucleic acids during a hybridization assay.

Preferably, a predetermined region comprises at least 2, preferably at least 100 single-stranded polynucleotides, more preferably about 1000 single-stranded polynucleotides, and will usually not exceed 10,000 polynucleotide probes, that are complementary to a nucleic acid of the invention. Typically, a predetermined region is spotted with at least 2, usually at least 100 single-stranded polynucleotides of identical sequences. The predetermined region generally has an average size ranging from about 0.01 cm² to about 1 cm².

The substrates of the subject arrays may be manufactured from a variety of materials. In general, the materials with which the support is fabricated exhibit a low level of non-specific binding during hybridization assay. A preferred solid support is made from one or more of the following types of materials: nitrocellulose, nylon, polypropylene, glass, and silicon. The materials may be flexible or rigid. A flexible substrate is capable of being bent, folded, twisted or similarly manipulated, without breaking. A rigid substrate is one that is stiff or inflexible and prone to breakage. As such, the rigid substrates of the subject arrays are sufficient to provide physical support and structure to the polymeric targets present thereon under the assay conditions in which the arrays are employed, particularly under high throughput assay conditions. Exemplary materials suitable for fabricating flexible support include a diversity of membranous materials, such as nitrocellulose, nylon or derivatives thereof, and plastics (e.g. polytetrafluoroethylene, polypropylene, polystyrene, polycarbonate, and blends thereof). Examples of materials suitable for making rigid support include but are not limited to glass, semi-conductors such as silicon and germanium, metals such as platinum and gold. The solid support on which arrays of polynucleotide probes are attached comprises at least one surface, which may be smooth or substantially planar, or with irregularities such as depressions or elevations.

The surface on which the pattern of probes is deposited may be modified with one or more different layers of compounds that serve to modify the properties of the surface in a desirable manner. Modification layers coated on the solid support may comprise inorganic layers made of, e.g. metals, metal oxides, or organic layers composed of polymers or small organic molecules and the like. Polymeric layers of interest include layers of peptides, proteins, polysaccharides, lipids, phospholipids, polyurethanes, polyesters, polycarbonates, polyureas, polyamides, polyethyleneamines, polyarylene sulfates, polysiloxanes, polyimides, polyacetates and the like, where the polymers may be hetero- or homopolymeric, and may or may not be conjugated to functional moieties. Arrays of polynucleotide probes provide an effective means of detecting or monitoring expression of a multiplicity of genes and may be used in a wide variety of circumstances including identifying compounds useful for treating or preventing a neurodegenerative disorder, identification and quantification of differential gene expression between at least two samples, such as, for example a control sample and a sample contacted with a polypeptide of the invention, and/or screening for compositions of the invention that upregulate or downregulate the expression or alter the pattern of expression of particular genes that are involved in neurodegenerative disorders.

Where desired, the resulting transcribed nucleic acids may be amplified prior to hybridization. One of skill in the art will appreciate that whichever amplification method is used, if a quantitative result is desired, caution must be taken to use a method that maintains or controls for the relative copies of the amplified nucleic acids. Methods of “quantitative” amplification are well known to those of skill in the art. For example, quantitative PCR involves simultaneously co-amplifying a known quantity of a control sequence using the same primers. This provides an internal standard that may be used to calibrate the PCR reaction. The subject array may also include probes specific to the internal standard for quantification of the amplified nucleic acid. Detailed protocols for quantitative PCR are provided in PCR Protocols, A Guide to Methods and Applications, Innis et al., Academic Press, Inc. N.Y., 1990.

Suitable hybridization conditions for the practice of the present invention are such that the recognition interaction between the probe and target is both sufficiently specific and sufficiently stable. Hybridization reactions can be performed under conditions of different “stringency”. Relevant conditions include temperature, ionic strength, time of incubation, the presence of additional solutes in the reaction mixture such as formamide, and the washing procedure. Higher stringency conditions are those conditions, such as higher temperature and lower sodium ion concentration, which require higher minimum complementarity between hybridizing elements for a stable hybridization complex to form. Conditions that increase the stringency of a hybridization reaction are widely known and published in the art. See, for example, Sambrook, et al., supra.

For a convenient detection of the probe-target complexes formed during the hybridization assay, the target nucleic acids can be conjugated to a detectable label. Detectable labels suitable for use in the present invention include any composition detectable by spectroscopic, photochemical, biochemical, immunochemical, electrical, optical or chemical means. A wide variety of appropriate detectable labels are known in the art, which include luminescent labels, radioactive isotope labels, enzymatic or other ligands. In preferred embodiments, one will likely desire to employ a fluorescent label or an enzyme tag, such as digoxigenin, β-galactosidase, urease, alkaline phosphatase, peroxidase, or avidin/biotin complex.

The labels may be incorporated by any of a number of means well known to those of skill in the art. In one aspect, the label is simultaneously incorporated during the amplification step in the preparation of the target nucleic acids. Thus, for example, polymerase chain reaction (PCR) with labeled primers or labeled nucleotides can provide a labeled amplification product In a separate aspect, transcription reaction, as described above, using a labeled nucleotide (e.g. fluorescein-labeled UTP and/or CTP) or a labeled primer, incorporates a detectable label into the transcribed nucleic acids.

Alternatively, a label may be added directly to the original nucleic acid sample (e.g., mRNA, polyA, mRNA, cDNA, etc.) or to the amplification product after the amplification is completed. Means of attaching labels to nucleic acids are well known to those of skill in the art and include, for example nick translation or end-labeling (e.g. with a labeled RNA) by kinasing of the nucleic acid and subsequent attachment (ligation) of a nucleic acid linker joining the sample nucleic acid to a label (e.g., a fluorophore).

The detection methods used to determine where hybridization has taken place and/or to quantify the hybridization intensity will typically depend upon the label selected above. For example, radiolabels may be detected using photographic film or phosphoimager (for detecting and quantifying ³²P incorporation). Fluorescent markers may be detected and quantified using a photodetector to detect emitted light (see U.S. Pat. No. 5,143,854 for an exemplary apparatus). Enzymatic labels are typically detected by providing the enzyme with a substrate and measuring the reaction product produced by the action of the enzyme on the substrate; and finally colorimetric labels are detected by simply visualizing the colored label.

The detection method provides a positional localization of the region where hybridization has taken place. The position of the hybridized region correlates to the specific sequence of the probe, and hence the identify of the gene transcript expressed in the test subject. The detection methods also yield quantitative measurement of the level of hybridization intensity at each hybridized region, and thus a direct measurement of the level of expression of a given gene transcript. A collection of the data indicating the regions of hybridization present on an array and their respective intensities constitutes a “hybridization pattern” that is representative of a multiplicity of expressed gene transcripts of a subject. Any discrepancies detected in the hybridization patterns generated by hybridizing target nucleic acids derived from different subjects are indicative of differential expression of a multiplicity of gene transcripts of these subjects.

One of skill in the art, however, will appreciate that hybridization signals will vary in strength with efficiency of hybridization, the amount of label on the target nucleic acid and the amount of particular target nucleic acid in the sample. Typically target nucleic acids present at very low levels (e.g., <1 pmol) will show a weak signal. In evaluating the hybridization data, a threshold intensity value may be selected below which a signal is not counted as being essentially indistinguishable from background. In addition, the provision of appropriate controls permits a more detailed analysis that controls for variations in hybridization conditions, cell health, non-specific binding and the like. The subjects employed for the comparative hybridization analysis may be cells treated with or without external or internal stimuli. Thus, the comparative hybridization analysis using the arrays described herein can be employed to monitor gene expression in a wide variety of contexts. Such analysis may be extended to detecting differential expression of genes between diseased and normal tissues, or amongst cells that are subjected to various environmental stimuli or candidate drugs, such as the polypeptides of the present invention.

Assays for Measuring Expression Levels

The screening methods of the invention may be used to identify candidate compounds that modulate the expression levels of any of the polypeptides listed in Table 4 or Table 5 by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 100% relative to an untreated control. According to one approach, candidate compounds are added at varying concentrations to the culture medium of cells expressing the polypeptide of Table 4 or Table 5. Gene expression of the polypeptide is then measured, for example, by standard Northern blot analysis (Ausubel et al., supra), using any appropriate fragment prepared from the nucleic acid molecule encoding the polypeptide as a hybridization probe or by real time PCR with appropriate primers. The level of gene expression in the presence of the candidate compound is compared to the level measured in a control culture medium lacking the candidate molecule. If desired, the effect of candidate compounds may, in the alternative, be measured at the protein level using the same general approach and standard immunological techniques, such as Western blotting or immunoprecipitation with an antibody specific to the polypeptide for example. For example, immunoassays may be used to detect or monitor the level of the polypeptide from Table 4 or Table 5. Polyclonal or monoclonal antibodies which are capable of binding to such polypeptides may be used in any standard immunoassay format (e.g., ELISA or RIA assay) to measure protein levels of the polypeptide. The polypeptide of the invention can also be measured using mass spectroscopy, high performance liquid chromatography, spectrophotometric or fluorometric techniques, or combinations thereof.

Reporter Gene Assays

Expression of a reporter gene that is operably linked to the promoter of a gene identified in Tables 4 or 5, (e.g., an NT-3, VIP, CGRP, CCK-8, or GRP promoter) can also be used to identify a candidate compound for treating or preventing PD. Assays employing the detection of reporter gene products are extremely sensitive and readily amenable to automation, hence making them ideal for the design of high-throughput screens. Assays for reporter genes may employ, for example, calorimetric, chemiluminescent, or fluorometric detection of reporter gene products. Many varieties of plasmid and viral vectors containing reporter gene cassettes are easily obtained. Such vectors contain cassettes encoding reporter genes such as lacZ/β-galactosidase, green fluorescent protein, and luciferase, among others. A genomic DNA fragment carrying a selected transcriptional control region (e.g., a promoter and/or enhancer) is first cloned using standard approaches (such as those described by Ausubel et al. (supra). The DNA carrying the selected transcriptional control region is then inserted, by DNA subcloning, into a reporter vector, thereby placing a vector-encoded reporter gene under the control of that transcriptional control region. The activity of the selected transcriptional control region operably linked to the reporter gene can then be directly observed and quantified as a function of reporter gene activity in a reporter gene assay.

In one embodiment, for example, the transcriptional control region could be cloned upstream from a luciferase reporter gene within a reporter vector. This could be introduced into the test cells, along with an internal control reporter vector (e.g., a lacZ gene under the transcriptional regulation of the β-actin promoter). After the cells are exposed to the test compounds, reporter gene activity is measured and the reporter gene activity is normalized to internal control reporter gene activity.

Assays Measuring Biological Activity

Based on this invention, a candidate compound may be tested for its ability to modulate the biological activity of one or more polypeptides listed in Table 4 or Table 5 in cells that naturally express such a polypeptide, after transfection with a cDNA for this polypeptide, or in cell-free solutions containing the polypeptide, as described further below. Accordingly, candidate compounds are first contacted with a polypeptide from either table, having some level of a characteristic biological activity (including cell survival). The exact level of activity is unimportant and may be at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or more than 100% of the biological activity of the naturally-occurring, wild-type polypeptide. The effect of a candidate compound on the activity of the polypeptide can be tested by radioactive and non-radiaoactive binding assays, competition assays, and receptor signaling assays.

In one example, a cell (e.g., a primary VMDA) expressing the polypeptide of Table 4 or Table 5 is contacted with a candidate compound, after which the biological activity (e.g., survival of a cell or any one of the activities associated with the naturally-occurring polypeptide) of the polypeptide is measured in the cell. In another example, contacting between candidate compounds and polypeptides occurs in a cell-free system or in an animal, and biological activity is then determined. Biological activity may be determined using any standard method, including those described herein. A candidate compound that modulates such biological activity relative to that of the same polypeptide in a cell not contacted with the candidate compound, identifies the candidate compound as being useful for treating or preventing neurodegenerative disorders.

Candidate compounds of the present invention may also be identified based on their ability to increase the growth or survival of cells (e.g., dopaminergic cells) that express one of a panel of target polypeptides. For example, a candidate compound may be contacted with a plurality of cell populations, such that each contacting event is segregated from the others. Each population of cells expresses a polypeptide listed in Table 4 or Table 5. A candidate compound that increases the growth or survival of at least two populations of cells expressing such polypeptides, relative to the growth or survival of control populations not contacted with the candidate compound, is identified as a compound having the ability to treat or prevent neurodegenerative disorders. Optionally, assays measuring cell growth or cell survival may also be employed to confirm that a candidate compound identified by any of the other assays of the invention (e.g., assays detecting expression levels or biological activity (other than cell survival) of the polypeptides) can effectively increase cell survival.

If the contacting event occurs in vivo, the biological activity of the candidate compound may be assessed by determining the survival of treated animals relative to untreated animals, the reduction in neurodegenerative symptoms (e.g., neuronal atrophy) in treated animals relative to untreated animals, or both.

Candidate Compounds

Candidate compounds (e.g., organic molecules, peptides, peptide mimetics, polypeptides, nucleic acids, or antibodies) may be obtained using any of the numerous approaches in combinatorial library methods known in the art, including: biological libraries; spatially addressable parallel solid phase or solution phase libraries; synthetic library methods requiring deconvolution; the ‘one-bead one-compound’ library method; and synthetic library methods using affinity chromatography selection. The biological library approach is limited to peptide libraries, while the other four approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds (see e.g., Lam, Anticancer Drug Des. 12:145, 1997).

Examples of methods for the synthesis of molecular libraries can be found in the art, for example in: DeWitt et al., Proc. Natl. Acad Sci. USA. 90:6909, 1993; Erb et al., Proc. Natl. Acad Sci. USA 91:11422, 1994; Zuckermann et al., J. Med. Chem. 37:2678, 1994; Cho et al., Science 261:1303, 1993; Carrell et al., Angew. Chem. Int. Ed. Engl. 33:2059, 1994; Carell et al., Angew. Chem. Int. Ed. Engl. 33:2061, 1994; and Gallop et al., J. Med. Chem. 37:1233, 1994. Libraries of compounds may be presented in solution (Houghten, Biotechniques 13:412-421, 1992), or on beads (Lam, Nature 354:82-84, 1991), chips (Fodor, Nature 364:555-556, 1993), bacteria (Ladner U.S. Pat. No. 5,223,409), spores (Ladner U.S. Pat. No. 5,223,409), plasmids (Cull et al., Proc. Natl. Acad. Sci. USA 89:1865-1869, 1992) or on phage (Scott et al., Science 249:386-390, 1990; Devlin, Science 249:404-406, 1990; Cwirla et al., Proc. Natl. Acad. Sci. 87:6378-6382 1990; Felici, J. Mol. Biol. 222:301-310, 1991).

Optionally, either the polypeptide of Table 4 or Table 5 or the candidate compound may include a label or tag that facilitates their isolation. For polypeptides, an exemplary tag of this type is a poly-histidine sequence generally containing around six histidine residues that permits the isolation of a compound so labeled by means of nickel chelation. Other labels and tags, such as the FLAG tag (Eastman Kodak, Rochester, N.Y.), are well known and are routinely used in the art. Small molecules may be radiolabeled for detection.

Candidate Compounds: Polypeptides and Proteins

For their use in the present invention as candidate compounds, recombinant polypeptides, particularly polypeptides of Table YY, may be produced using any standard technique known in the art. Following their production, these polypeptides are useful, for example, for the identification of therapeutic compounds using the methods described herein.

Host cells, such as yeast, bacterial, mammalian, and insect cells, may produce any of the polynucleotides of the present invention. These cells may produce such polynucleotides endogenously or may alternatively be genetically engineered to do so. Polynucleotides may be introduced into host cells using any standard method known in the art, including, for example, calcium phosphate transfection, DEAE-dextran mediated transfection, transvection, microinjection, cationic lipid-mediated transfection, electroporation, transduction, ballistic introduction, and infection or fusion with carriers such as liposomes, micelles, ghost cells, and protoplasts.

In general, any expression system or vector that is able to maintain, propagate, or express a polynucleotide to produce a polypeptide in a host may be used. These include chromosomal, episomal, and virus-derived systems such as vector-derived bacterial plasmids, bacteriophages, transposons, yeast episomes, insertion elements, yeast chromosomal elements, viruses (such as baculoviruses, papova viruses (e.g., SV40), vaccinia viruses, adenoviruses, fowl pox viruses, pseudorabies viruses, and retroviruses), and vectors derived from combinations thereof, such as those derived from plasmid and bacteriophage genetic elements, such as cosmids and phagemids. Preferred expression vectors include, but are not limited to, pcDNA3 (Invitrogen) and pSVL (Pharmacia Biotech). Other exemplary expression vectors include pSPORT vectors, pGEM vectors (Promega), pPROEXvectors (LTI, Bethesda, Md.), Bluescript vectors (Stratagene), pQE vectors (Qiagen), pSE420 (Invitrogen), and pYES2 (Invitrogen). Optionally, the expression systems may contain control regions that facilitate or regulate expression. The appropriate polynucleotide may be inserted into an expression system by any of a variety of well-known and routine techniques, including transformation, transfection, electroporation, nuclear injection, or fusion with carriers such as liposomes, micelles, ghost cells, and protoplasts.

Expression systems of the invention include bacterial, yeast, fungal, plant, insect, invertebrate, vertebrate, and mammalian cells systems. If a eukaryotic expression vector is employed, then the appropriate host cell is any eukaryotic cell capable of expressing the cloned sequence. Preferably, eukaryotic cells are cells of higher eukaryotes. Suitable eukaryotic cells include non-human mammalian tissue culture cells and human tissue culture cells. Preferred host cells include insect cells, HeLa cells, Chinese hamster ovary cells (CHO cells), African green monkey kidney cells (COS cells), human 293 cells, murine embryonal stem (ES) cells, and murine 3T3 fibroblasts. The propagation of such cells in cell culture is standard in the art. Yeast hosts may also be employed as a host cell. Preferred yeast cells include the genera Saccharomyces, Pichia, and Kluveromyces. Preferred yeast hosts are Saccharomyces cerevisiae and Pichia pastoris. Yeast vectors may contain any of the following elements: an origin of replication sequence from a 2T yeast plasmid, an autonomous replication sequence (ARS), a promoter region, sequences for polyadenylation, sequences for transcription termination, and a selectable marker gene. Shuttle vectors for replication in both yeast and E. coli are also included herein.

Alternatively, insect cells may be used as host cells. In a preferred embodiment, the polypeptides of the invention are expressed using a baculovirus expression system. The Bac-to-Bac complete baculovirus expression system (Invitrogen) may be used, for example, for protein production in insect cells.

Expression of polypeptides in prokaryotes is most often carried out in E. coli with vectors containing constitutive or inducible promoters directing the expression of either fusion or non-fusion proteins. Fusion vectors add a number of amino acids to a polypeptide encoded therein, usually to the amino terminus of the recombinant polypeptide. Such fusion vectors typically serve three purposes: 1) to increase expression of recombinant protein; 2) to increase the solubility of the recombinant protein; and 3) to aid in the purification of the recombinant protein by acting as a ligand in affinity purification. Often, in fusion expression vectors, a proteolytic cleavage site is introduced at the junction of the fusion moiety and the recombinant polypeptide to enable separation of the recombinant protein from the fusion moiety subsequent to purification of the fusion protein. Such enzymes, and their cognate recognition sequences, include Factor Xa, thrombin, and enterokinase. Typical fusion expression vectors include pGEX, pMAL, and pRIT5, which fuse glutathione S-transferase (GST), maltose E binding protein, and protein A, respectively, to the target recombinant protein.

The polypeptides of the present invention may also be expressed at the surface of cells, which are then harvested prior to use in the screening assay. If the polypeptide is secreted into the medium, the medium may be recovered in order to recover and purify the polypeptide. If produced intracellularly, the cells must first be lysed before the polypeptide is recovered. Polypeptides of the present invention may be recovered and purified from recombinant cell cultures or lysates by well-known methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxyapatite chromatography, and lectin chromatography. Most preferably, high performance liquid chromatography is employed for purification. Well-known techniques for refolding proteins may be employed to regenerate active conformation when the polypeptide is denatured during intracellular synthesis, isolation, and/or purification.

Optionally, the polypeptides of the present invention may be prepared by chemical synthesis using, for example, automated peptide synthesizers.

Materials and Methods

Laser Capture Microdissection (LCM)

Tissue Preparation

Adult C57/B6 mice (Jackson Laboratory, West Grove, Pa.) were anesthetized with intraperitoneal (i.p.) sodium pentobarbital (300 mg/kg) and decapitated. The brain was removed, snap-frozen in dry ice-cooled 2-methylbutane (−60° C.), and embedded in frozen tissue medium (Tissue Tek OTC, Sakura Finetek USA, Torrance, Calif.). Twelve micron-thick coronal sections of the midbrain were cut using a cryostat, mounted on LCM slides (Arcturus), and immediately stored at −70° C.

Quick Immunostaining and Dehydration of Sections

A quick immunostaining protocol against tyrosine hydroxylase (TH) was used to identify the dopaminergic neurons to be captured. The tissue sections will be fixed in cold 70% ethanol for 15 seconds, followed by 5 minutes fixation in cold acetone. Slides were washed in PBS, incubated with rabbit anti-TH (Pel-Freez Biologicals, Rogers, Ark.; 1:25) for 5 min, washed in PBS, and exposed to biotinylated anti-rabbit antibody (Vector Laboratories, Burlingame, Calif.; 1:300) for 5 minutes. Slides were washed in PBS, incubated in ABC-horseradish peroxidase enzyme complex (Vectastain, Vector Laboratories) for 5 min and the staining was detected with the substrate, diaminobenzidine (DAB). Sections were subsequently dehydrated in graded ethanol solution (1 min each in water, 70% ethanol, 95% ethanol, 100% ethanol, and twice for 5 min in xylene).

LCM of Mouse Midbrain Tissue

The PixCell II System (Arcturus Engineering, Inc, Mountain View, Calif.) was used for LCM. Approximately one thousand neurons were captured in each region of A9 and A10 in each animal. Since ventrolateral A9 cells are the most vulnerable and medial A10 cells are the most resistant to degeneration, only ventrolateral A9 (ventrolateral SNc, substantia nigra pars reticulata (SNr), substantia nigra pars lateralis (SNpl)) and medial A10 cells (central linear nucleus (CLi), interfascicular nucleus (IF), medial VTA, medial nucleus paranigralis (PN), medial nucleus parabrachialis pigmentosus (PBN)) were microdissected (FIGS. 1A-1D).

Affymetrix GeneChip Microarrays

Sample and Array Processing Total RNA was extracted from the individual samples using the PicoPure RNA isolation kit (Arcturus, Mountain View, Calif.). RNA quality was assessed by electrophoresis using the Agilent Bioanalyzer 2100 and spectrophotometric analysis prior to sample processing. Nanogram quantities of total RNA from each sample was used to generate a high fidelity cDNA, which is modified at the 3′ end to contain an initiation site for T7 RNA polymerase. Upon completion of cDNA synthesis all of the product was used in an in vitro transcription (IVT) reaction to generate aRNA. Up to 2 ug of aRNA was used for a second round of amplification that was initiated by random hexamer priming for first strand cDNA synthesis. The second round IVT contained biotinylated UTP and CTP which are utilized for detection following hybridization to the oligonucleotide microarray. 20 μg of full-length cRNA, from both control and enriched samples, were fragmented and hybridized to GeneChip arrays following the manufacturer's protocol. All samples were subjected to gene expression analysis via the Affymetrix Murine 430A high-density oligonucleotide array, which queries 22,000 mouse probe sets. Protocols for target hybridization, washing and staining were performed as per the manufacturer's protocol (http://www.affymetrix.com).

Data Normalization and Statistical Analysis

Several complementary data analysis approaches were used to identify differentially expressed genes. The Gene Chip Operating System 1.0 (GCOS, Affymetrix) was employed to generate one approach to comparative analysis presented in this study. Distinct algorithms were used to determine the absolute call, which distinguishes the presence or absence of a transcript, the differential change in gene expression and the magnitude of change, which is represented as signal log ratio (on a log base 2 scale). The mathematical definitions for each of these algorithms can be found in the GCOS data analysis guide. Two additional low level analysis methods were applied to all data sets outside of the Affymetrix normalization schema. Iobion's GeneTraffic MULTI was used to perform Robust Multi-Chip Analysis (RMA), which is a median polishing algorithm used in conjunction with both background subtraction and quantile normalization approaches. For each normalization approach, statistical analysis using the Significance Analysis Tool set in GeneTraffic was utilized. A two class unpaired analytical approach employing Benjamini-Hochberg correction for false discovery rate (FDR) was used for all probe level normalized data. Gene lists of differentially expressed genes were generated from this output for functional analysis. All data were organized in a central database in the University of Rochester Functional Genomics Center and is accessible through the following URL (www.fgc.urmc.rochester). Following each of these normalization approaches all genes differentially expressed were clustered based on biological relevance utilizing both hierarchical and K-means clustering techniques. Lastly, PathwayAssist (Iobion Informatics) was employed to build functional networks of differentially expressed genes.

Realtime PCR for Candidate Gene Validation

RNA samples from A9 and A10 DA neurons obtained from LCM were reverse-transcribed into cDNA using Sensiscript reverse transcriptase (Qiagen, Valencia, Calif.) and oligo dT as the primer. PCR reactions were set up in 25 μl reaction volume using SYBR Green PCR Master Mix (Applied Biosystems, Foster City, Calif.). Primers for each candidate gene were designed using MacVacter 7.0 and used with final concentration of 250 nM. For each primer pairs, duplicates of three to five independently collected A9 and A10 samples were compared to quantify relative gene expression differences between these cells using 2^−ΔΔCT method. Beta-actin was used as an internal control gene and primers for candidate genes with approximately equal (within 5% difference) amplification efficiency to that of the internal control were chosen.

Gene Transfer Using Lentivirus

Recombinant viruses, such as herpes simplex virus (HSV-1) and derivatives, Adenovirus (Ad), Adeno Associated Virus (AAV) and Lentivirus (LV) are effective vehicles for gene transfer to the adult CNS. Among these viruses, the LVs have several advantages, which make them an attractive tool for gene delivery to the brain. This includes a large cloning capacity (up to 9 kbp), stable integration into the genome of non-dividing cells, long-term gene expression, and high transduction efficiency of cells in both striatum and substantia nigra. The current third generation of LVs used in our studies has several features to reduce the risk of recombination events, such as the elimination of about 60% of the viral genome, the generation of virus particles with a four plasmid transfection system, and the introduction of self-inactivation. The efficiency of the LVs was also improved by pseudotyping with the vesicular stomatitis virus (VSV-G) envelope protein and the introduction of transcriptional and transduction enhancers into the virus backbone, such as the woodchuck virus regulatory element (WPRE) and a pol-derived poly pyrimidine tract (cPPT), respectively. Recombinant LVs have been successfully used in a variety of settings with high transduction and expression efficiencies including the brain. In particular, recombinant LVs expressing GDNF have been effective as a neuroprotective treatment in both rodent and primate models of PD.

Construction of Lentiviral Vectors

Mouse GIRK2 cDNA was cloned into lentiviral vector, pRRL.cPPT.PGK.GFP. W.Sin-18 vector. Virus constructs was confirmed by sequence analyses.

Production of Lentiviral Vectors and Cell Transduction

High titer of infectious lentiviral particles were produced in 293 T cells using a four-plasmid transfection protocol (Current Protocols in Neuroscience, 2000, 4.21.1-4.21.12). The packaging plasmids pMDLg/pRRE (for gag and pol expression), pMD.G (for expression of the VSV-G env protein), and pRSV.Rev (for rev expression) were co-transfected with the recombinant pRRL.cPPT.PGK.W.Sin-18 vectors to produce viral transduction units (TU). Virus supernatants were collected and filtered through a 0.2 μm filter and either used freshly, stored at −80° C. or ultracentrifuged to obtain high concentrations of viral stocks. Virus titers were determined by measuring the viral capsid protein p24 by ELISA. For in vitro transduction, PC12-αSyn were cultured directly in virus-containing media supplemented with 8 μg/ml polybrene.

Detection of Cell Death

Cell death will be assessed by quantifying intra- and extracellular lactate dehydrogenase (LDH). The ratio between the amount of LDH released and the amount remaining in the cells produces a measure of cell death. $\mathrm{Cell}\mathrm{death}\propto \frac{\mathrm{extracellular}\mathrm{LDH}}{\mathrm{total}\mathrm{LDH}}$

A sample of the medium will be the extracellular LDH sample. Cells were washed with PBS and extracted in cell lysis buffer (50 mM Tris pH 8.0, 150 mM NaCl, 5 mM EDTA, 1% Triton X-100, 10 μg/ml Aprotinin, 25 μg /ml Leupeptin, 10 μg/ml Pepstatin, 1 mM PMSF; all protease inhibitors purchased from Sigma Chemicals, St. Louis, Mo.). The cell homogenate were centrifuged at 4° C. for 3 minutes at 14,000 rpm. The supernatant were taken for intracellular LDH sample. LDH activity will be quantified using an LDH assay kit (Roche, Indianapolis, Ind.).

Apoptotic nuclei may be detected using TUNEL (ApopTag™, Serologicals Corporation, Norcross, Ga.). This technique tails nucleosome-sized DNA fragments with digoxigenin-dNTP followed by antibody conjugation. Nuclei may be counterstained with Hoechst 33342 (Molecular Probes, Eugene, Oreg.). Apoptosis may be quantified by a blinded assessor and expressed as the percentage of nuclei that are TUNEL-positive in two randomly selected 20× fields.

Immunocytochemistry

Routine indirect immunofluorescence was performed on 4% paraformaldehyde fixed VM culture. The fixed cells were incubated in a blocking solution consisting of 10% normal donkey serum (Jackson Immuno Research Laboratories Inc, West Grove, Pa.) and 0.1% Triton X-100 (Sigma, St. Louis, Mo.) in 0.1M phosphate buffered saline (PBS) for 1 hour at room temperature before transferring to the primary antibody solution. The primary antibodies were diluted in blocking solution and the cells were incubated overnight at 4° C. The primary antibodies used were raised against tyrosine hydroxylase (sheep anti-TH, 1:300, Pel-Freez Biologicals, Rogers, Ak.) and GIRK2 (rabbit; 1:80, Alomone Laboratories, Jerusalem, Israel). The cells were rinsed three times in 0.1 M PBS for five minutes each before the application of the secondary antibody solution for one hour at room temperature. The secondary antibodies were diluted in 10% normal donkey serum in 0.1M PBS. The secondary antibodies were conjugated to spectrally distinct fluorescent dyes to facilitate color separation (Alexa Fluor 488 conjugated donkey anti-sheep and Alexa Fluor 594 conjugated donkey anti-rabbit, Molecular Probes, Eugene, Oreg.). After rinsing in triplicate for ten minutes each in 0.1 M PBS, the cells were counterstained with 0.0005% Hoechst 33342 (Molecular Probes) in 0.1M Tris buffered saline. The coverslips containing the fixed cells were then rinsed in 0.1M PBS followed by distilled water and mounted onto slides using an aqueous mountant (Gel/Mount, Biømeda Corp., Calif.). Control coverslips immunostained without primary antibody were used to assess specificity of the technique.

Stereology

Design based stereology was performed by counters blinded to experimental groups on the stained coverslips using an integrated Axioskop 2 microscope (Carl Zeiss, Thornwood, N.Y.) and Stereoinvestigator image capture equipment and software (MicroBrightField, Williston, Vt.). A contour was drawn around each coverslip to identify the area of interest. A physical disector probe was utilized and counting frames were placed in a systematically random manner at approximately 125 sites per coverslip. The resultant coefficient of error for the stereological counts was used to assess precision (p<0.05).

Semiquantitative RT-PCR

One to three micrograms of amplified RNA was transcribed into cDNA with the SuperScript™ Preamplification Kit (Life Technologies) and random hexamers. The PCR reactions were carried out with 1×IN Reaction Buffer (Epicentre Technologies, Madison, Wis.), 1.4 nm of each primer, and 2.5 units of Taq I DNA polymerase (Promega, Madison, Wis.). Samples were amplified in an Eppendorf Thermocycler (Brinkmann Instruments, Westbury, N.Y.) under the following conditions: denaturing step at 95° C., 40 sec; annealing step at 55° C., 30 sec; amplification step at 72° C., 1 min for 20-30 cycles and a final amplification step at 72° C., 10 min. For semiquantitative RT-PCR, cDNA templates were normalized by β-actin-specific transcript and levels of gene transcription were detected by adjusting PCR cycling and primer design in such a way that each primer set amplified its corresponding gene product within a linear range, avoiding saturation of signals.

Quantitative Real Time PCR (Q-PCR)

RNA can be reverse transcribed to cDNA using Sensiscript (Qiagen, Valencia, Calif.) reverse transcriptase (RT) with oligo dT primer. RT reaction is performed at 37° C. for 1 hour and will be followed by inactivation of the enzyme at 93° C. for 5 min. Q-PCR may be performed using SYBR Green PCR master mix (PE Applied Biosystems, Foster City, Calif.). PCR mixture contains optimized concentrations of forward and reverse primers, cDNA and 1×SYBR Green PCR master mix. PCR amplification is performed as followed: 95° C. for 10 min, 49 cycles of 95° C. for 30 sec, 55° C. for 30 sec, 72° C. for 30 sec on a DNA Engine Opticon (MJ Research, Waltham, Mass.). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and β-actin will be used as an internal control. The fold change in A9 and A10 cDNA relative to the internal controls is determined by: Fold change=2^−ΔΔCt, whereΔΔCt=(Ct_A9−Ct_{internal control})−(Ct_A10−Ct_{internal control}).

TABLE 4
Genes Overexpressed by at Least 1.5 Fold in A9 Cells Relative to A10 Cells
	Fold
Gene ID	Induction	UniGene Name	UniGene Symbol	Representative mRNA Accession
1418601_at	5.89	aldehyde dehydrogenase family 1,	Aldhla7	NM_011921 // aldehyde
		subfamily A7		dehydrogenase family 1, subfamily A7
1449571_at	5.56	thyrotropin releasing hormone receptor	Trhr	NM_013696 // thyrotropin releasing hormone receptor
1437502_x_at	4.07	CD24a antigen	Cd24a	NM_009846 // CD24a antigen
1448182_a_at	3.92	CD24a antigen	Cd24a	NM_009846 // CD24a antigen
1423136_at	3.57	fibroblast growth factor 1	Fgf1	NM_010197 // fibroblast growth factor 1
1449494_at	3.28	RAB3C, member RAS oncogene family	Rab3c	NM_023852 // RAB3C, member RAS oncogene family
1449348_at	3.23	membrane protein, palmitoylated 6	Mpp6	NM_019939 // membrane protein,
		(MAGUK p55 subfamily member 6)		palimitoylated 3 (MAGUK p55 subfamily member 6)
1448954_at	3.17	RIKEN cDNA A330103B05 gene	A330103B05Rik	NM_020610 // RIKEN cDNA A330103B05
1449254_at	2.92	secreted phosphoprotein 1	Spp1	NM_009263 // secreted phosphoprotein 1
1452656_at	2.90	zinc finger, DHHC domain containing 2	Zdhhc2	NM_178395 // zinc finger, DHHC domain containing 2
1423287_at	2.87	cerebellin 1 precursor protein	Cbln1	NM_019626 // cerebellin 1 precursor protein
1449245_at	2.84	glutamate receptor, ionotropic, NMDA2C	Grin2c	NM_010350 // glutamate receptor,
		(epsilon 3)		ionotropic, NMDA2C (epsilon 3)
143860_x_at	2.74	solute carrier family 25 (mitochondrial	Slc25a5	NM_007451 // solute carrier family 25, member 5
		carrier; adenine nucleotide translocator),
		member 5
1418104_at	2.73	RIKEN cDNA A330103B05 gene	A330103B05Rik	NM_020610 // RIKEN cDNA A330103B05
1422520_at	2.73	neurofilament 3, medium	Nef3	NM_008691 // neurofilament 3, medium
1448673_at	2.70	poliovirus receptor-related 3	Pvrl3	NM_021495 // poliovirus receptor-related 3 ///
				NM_021496 // nectin-3beta /// NM_021497 //
				nectin-3 gamma
1421534_at	2.65	fibroblast growth factor inducible 15	Fin15	NM_008016 // fibroblast growth factor inducible 15
1438945_x_at	2.56	gap junction membrane channel protein	Gja1	NM_010288 // gap junction membrane
		alpha 1		channel protein alpha 1
1417071_s_at	2.54	cytochrome P450, family 4, subfamily v,	Cyp4v3	NM_133969 // family 4 cytochrome P450
		polypeptide 3
1415800_at	2.51	gap junction membrane channel protein	Gja1	NM_010288 // gap junction
		alpha 1		membrane channel protein alpha 1
1436182_at	2.50	special AT-rich sequence binding protein 1	Satb1	NM_009122 // special
				AT-rich sequence binding protein 1
1438922_x_at	2.50	solute carrier family 25 (mitochondrial	Slc25a5	NM_007451 // solute carrier family 25, member 5
		carrier; adenine nucleotide translocator),
		member 5
1452583_s_at	2.49	RIKEN cDNA A530057M15 gene	A530057M15Rik	NM_176963 // aldose 1-epimerase
1427677_a_at	2.45	SRY-box containing gene 6	Sox6	NM_011445 // SRY-box containing gene 6
1437992_x_at	2.45	gap junction membrane channel protein	Gja1	NM_010288 // gap junction
		alpha 1		membrane channel protein alpha 1
1448600_s_at	2.43	vav 3 oncogene	Vav3	NM_020505 // vav 3 oncogene ///
				NM_146139 // vav 3 oncogene
1438782_at	2.42	axonal-associated cell adhesion molecule	Axcam	NM_007518 // /// NM_173004 //
				axonal-associated cell adhesion molecule
1415861_at	2.34	tyrosinase-related protein 1	Tyrp1	NM_031202 // tyrosinase-related protein 1
1452142_at	2.32	gamma-aminobutyric acid (GABA-A)	Gabt1	NM_178703 // gamma-aminobutyric
		transporter 1		acid (GABA-A) transporter 1
1422600_at	2.31	RAS protein-specific guanine nucleotide-	Rasgrf1	NM_011245 // RAS protein-specific
		releasing factor 1		guanine nucleotide-releasing factor 1
1425846_a_at	2.27	calneuron 1	Caln1	NM_021371 // calneuron 1
1437401_at	2.27	insulin-like growth factor 1	Igf1	NM_010512 // insulin-like growth factor 1 ///
				NM_184052 // insulin-like growth factor 1
1421349_x_at	2.25	BM88 antigen	Bm88-pending	NM_021316 // BM88 antigen
1421841_at	2.24	fibroblast growth factor receptor 3	Fgfr3	NM_008010 // fibroblast growth factor receptor 3
1423286_at	2.23	cerebellin 1 precursor protein	Cbln1	NM_019626 // cerebellin 1 precursor protein
1434801_x_at	2.15	solute carrier family 25 (mitochondrial	Slc25a5	NM_007451 // solute carrier family 25, member 5
		carrier; adenine nucleotide translocator),
		member 5
1419225_at	2.11	calcium channel, voltage dependent,	Cacna2d3	NM_009785 // calcium channel,
		alpha2/delta subunit 3		voltage dependent, alpha2/delta subunit 3
1427019_at	2.11	protein tyrosine phosphatase, receptor	Ptprz1	NM_011219 // protein tyrosine
		type, Z polypeptide 1		phosphatase, receptor type, Z polypeptide 1 isoform 1 ///
				phosphatase, receptor type, Z polypeptide 1 isoform 2
1450878_at	2.11	RIKEN cDNA 2210417O06 gene	2210417O06Rik	NM_025618 // RIKEN cDNA 2210417O06
1438650_x_at	2.08	gap junction membrane channel protein	Gja1	NM_010288 // gap junction
		alpha 1		membrane channel protein alpha 1
1421180_at	2.07	limb expression 1 homolog (chicken)	Lix1	NM_025681 // limb expression 1 homolog
1416561_at	2.07	glutamic acid decarboxylase 1	Gad1	NM_008077 // glutamic acid decarboxylase 1
1417788_at	2.05	synuclein, gamma	Sncg	NM_011430 // synuclein, gamma
1436027_at	2.04	oxysterol binding protein-like 11	Osbpl11	NM_176840 // oxysterol binding protein-like 11
1416007_at	2.04	special AT-rich sequence binding protein 1	Satb1	NM_009122 // special AT-rich
				sequence binding protein 1
1434449_at	2.03	aquaporin 4	Aqp4	NM_009700 // aquaporin 4
1427919_at	2.03	RIKEN cDNA 1110039C07 gene	1110039C07Rik	NM_026838 // sushi-repeat containing protein
1432432_a_at	2.03	RAB3C, member RAS oncogene family	Rab3c	NM_023852 // RAB3C, member RAS oncogene family
1422706_at	2.03	Mus musculus, clone IMAGE: 5370952,	NA	NA
		mRNA
1425542_a_at	2.01	protein phosphatase 2, regulatory subunit	Ppp2r5c	NM_012023 // gamma isoform of
		B (B56), gamma isoform		regulatory subunit B56, protein phosphatase 2A
1435176_a_at	2.00	inhibitor of DNA binding 2	Idb2	NM_010496 // inhibitor of DNA binding 2
1439263_at	2.00	Mus musculus transcribed sequences	NA	NA
1434893_at	2.00	Mus musculus, clone IMAGE: 1365759,	NA	NA
		mRNA
1419519_at	1.98	insulin-like growth factor 1	Igf1	NM_010512 // insulin-like growth factor 1 ///
				NM_184052 // insulin-like growth factor 1
1436736_x_at	1.98	DNA segment, human D4S114	D0H4S114	NM_053078 // neuronal protein 3.1
1423854_a_at	1.97	RIKEN cDNA 1190017B18 gene	1190017B18Rik	NA
1423772_x_at	1.97	solute carrier family 25 (mitochondrial	Slc25a5	NM_007451 // solute carrier family 25, member 5
		carrier; adenine nucleotide translocator),
		member 5
1416183_a_at	1.97	lactate dehydrogenase 2, B chain	Ldh2	NM_008492 // lactate dehydrogenase 2, B chain
1425149_a_at	1.95	phosducin-like	Pdc1	NM_026176 // phosducin-like
1448955_s_at	1.94	Ca<2+>dependent activator protein for	Cadps	NM_012061 // Ca<2+>dependent
		secretion		activator protein for secretion
1421348_a_at	1.93	BM88 antigen	Bm88-pending	NM_021316 // BM88 antigen
1426283_at	1.93	RIKEN cDNA 6230410L23 gene	6230410L23Rik	NA
1416148_at	1.93	lysosomal-associated protein	Laptm4b	NM_033521 // lysosomal-associated
		transmembrane 4B		protein transmembrane 4B
1448213_at	1.93	annexin A1	Anxa1	NM_010730 // annexin A1
1448334_a_at	1.92	cyclin I	Ccni	NM_017367 // cyclin I
1448987_at	1.92	acetyl-Coenzyme A dehydrogenase, long-	Acad1	NM_007381 // acetyl-Coenzyme
		chain		A dehydrogenase, long-chain
1424988_at	1.91	myosin regulatory light chain interacting	Mir-pending	NM_153789 // myosin regulatory
		protein		light chain interacting protein
1427186_a_at	1.90	myocyte enhancer factor 2A	Mef2a	NA
1423288_s_at	1.89	cerebellin 1 precursor protein	Cbln1	NM_019626 // cerebellin 1 precursor protein
1416200_at	1.89	RIKEN cDNA 9230117N10 gene	9230117N10Rik	NM_133775 // RIKEN cDNA 9230117N10
1456395_at	1.89	RIKEN cDNA A830037N07 gene	A830037N07Rik	NM_177113 // RIKEN cDNA A830037N07 gene
1451190_a_at	1.89	SH3-binding kinase	Sbk-pending	NM_145587 // SH3-binding kinase
1448729_a_at	1.88	septin 4	38234	NM_011129 // peanut-like 2 homolog
1450839_at	1.88	DNA segment, human D4S114	D0H4S114	NM_053078 // neuronal protein 3.1
1452284_at	1.88	protein tyrosine phosphatase, receptor	Ptprz1	NM_011219 // protein tyrosine
		type, Z polypeptide 1		phosphatase, receptor type, Z polypeptide 1 isoform 1 ///
				NM_178180 // protein tyrosine phosphatase,
				receptor type, Z polypeptide 1 isoform 2
1424034_at	1.87	RAR-related orphan receptor alpha	Rora	NM_013646 // RAR-related orphan receptor alpha
1416749_at	1.85	protease, serine, 11 (Igf binding)	Prss11	NM_019564 // protease, serine, 11 (Igf binding)
1434229_a_at	1.85	polymerase (DNA directed), beta	Polb	NM_011130 // polymerase (DNA directed), beta
1434877_at	1.85	neuronal pentraxin 1	Nptx1	NM_008730 // neuronal pentraxin 1
1421129_a_at	1.85	ATPase, Ca++ transporting, ubiquitous	Atp2a3	NM_016745 // ATPase, Ca++ transporting, ubiquitous
1418929_at	1.83	estrogen-related receptor beta like 1	Esrrbl1	NM_028680 // huntingtin-
				interacting protein-1 protein interactor
1427344_s_at	1.83	RIKEN cDNA 4930526B11 gene	4930526B11Rik	NA
1416114_at	1.82	SPARC-like 1 (mast9, hevin)	Sparcl1	NM_010097 // SPARC-like 1 (mast9, hevin)
1438545_at	1.82	solute carrier family 25 (mitochondrial	Slc25a5	NM_007451 // solute carrier family 25, member 5
		carrier; adenine nucleotide translocator),
		member 5
1437874_s_at	1.81	hexosaminidase B	Hexb	NM_010422 // hexosaminidase B
1452123_s_at	1.81	RIKEN cDNA 6030440G05 gene	6030440G05Rik	NM_145148 // GRP1-binding protein GRSP1
1451313_a_at	1.81	RIKEN cDNA 1110067D22 gene	1110067D22Rik	NM_173752 // RIKEN cDNA 1110067D22
1424847_at	1.80	neurofilament, heavy polypeptide	Nefh	NA
1449312_at	1.80	neuropeptide Y receptor Y5	Npy5r	NM_016708 // neuropeptide Y receptor Y5
1448527_at	1.80	programmed cell death 10	Pdcd10	NM_019745 // programmed cell death 10
1438292_x_at	1.80	adenosine kinase	Adk	NM_007411 // /// NM_134079 // adenosine kinase
1451236_at	1.79	RAS-like, estrogen-regulated, growth-	Rerg	NM_181988 // RAS-like,
		inhibitor		estrogen-regulated, growth-inhibitor
1455239_at	1.79	Mus musculus, Similar to RIKEN cDNA	NA	NA
		6330512M04 gene, clone MGC: 58491
		IMAGE: 6534368, mRNA, complete cds
1452090_a_at	1.78	olfactomedin 3	Olfm3	NM_153157 // olfactomedin 3,
				isoformB /// NM_153458 // olfactomedin 3, isoform A
1424095_at	1.78	RIKEN cDNA 2310009A18 gene	2310009A18Rik	NM_025517 // RIKEN cDNA 2310009A18
1423312_at	1.75	trophoblast glycoprotein	Tpbg	NM_011627 // trophoblast glycoprotein
1422824_s_at	1.74	epidermal growth factor receptor pathway	Eps8	NM_007945 // epidermal growth factor
		substrate 8		receptor pathway substrate 8
1451991_at	1.73	Eph receptor A7	Epha7	NM_010141 // Eph receptor A7
1452283_at	1.73	expressed sequence AW123240	AW123240	NA
1453060_at	1.72	RIKEN cDNA 6530413N01 gene	6530413N01Rik	NM_026380 // RIKEN cDNA 6530413N01
1450940_at	1.72	ganglioside-induced differentiation-	Gdap1	NM_010267 // ganglioside-induced
		associated-protein 1		differentiation-associated-protein 1
1418758_a_at	1.72	pleckstrin homology, Sec7 and coiled-coil	Pscd3	NM_011182 // pleckstrin homology,
		domains 3		Sec7 and coiled-coil domains 3
1417318_at	1.71	deleted in bladder cancer chromosome	Dbccr1	NM_019967 // deleted in bladder cancer
		region candidate 1 (human)		chromosome region candidate 1
1415908_at	1.71	testis-specific protein, Y-encoded-like	Tspy1	NM_009433 // testis-specific protein, Y-encoded-like
1427004_at	1.71	F-box only protein 2	Fbxo2	NM_176848 // F-box only protein 2
1449929_at	1.70	t-complex-associated-testis-expressed 1-	Tcte11	NM_025975 // t-complex-
		like		associated-testis-expressed 1-like
1429318_a_at	1.70	quaking	Qk	NM_021881 // quaking protein
1421878_at	1.70	mitogen activated protein kinase 9	Mapk9	NM_016961 // mitogen activated protein kinase 9
1455534_s_at	1.70	oxysterol binding protein-like 11	Osbpl11	NM_176840 // oxysterol binding protein-like 11
1459903_at	1.70	RIKEN cDNA 2900057C09 gene	2900057C09Rik	NA
1434109_at	1.69	RIKEN cDNA A930014C21 gene	A930014C21Rik	NM_172507 // RIKEN cDNA A930014C21
1422823_at	1.69	epidermal growth factor receptor pathway	Eps8	NM_007945 // epidermal growth factor
		substrate 8		receptor pathway substrate 8
1430326_s_at	1.69	low molecular mass ubiquinone-binding	Qpc-pending	NM_025352 // low molecular
		protein		mass ubiquinone-binding protein
1455235_x_at	1.68	lactate dehydrogenase 2, B chain	Ldh2	NM_008492 // lactate dehydrogenase 2, B chain
1417403_at	1.68	ELOVL family member 6, elongation of	Elov16	NM_130450 // ELOVL family
		long chain fatty acids (yeast)		member 6, elongation of long chain fatty acids
1415930_a_at	1.68	microtubule-associated protein 1 light	Map1lc3	NM_026160 // microtubule-
		chain 3		associated protein 1 light chain 3
1416958_at	1.68	nuclear receptor subfamily 1, group D,	Nr1d2	NM_011584 // nuclear receptor
		member 2		subfamily 1, group D, member 2
1415783_at	1.68	vacuolar protein sorting 35	Vps35	NM_008582 // ///
				NM_022997 // vacuolar protein sorting 35
1424367_a_at	1.68	homer homolog 2 (Drosopila)	Homer2	NA
1428187_at	1.68	RIKEN cDNA 9130415E20 gene	9130415E20Rik	NM_175169 // RIKEN cDNA 9130415E20
1449921_s_at	1.68	copine Vl	Cpne6	NM_009947 // copine VI
1438606_a_at	1.67	DNA segment, Jeremy M. Boss 3	D0Jmb3	NA
1423907_a_at	1.67	NADH dehydrogenase (ubiquinone) Fe—S	Ndufs8	NM_144870 // NADH dehydrogenase
		protein 8		(ubiquinone) Fe—S protein 8
1436915_x_at	1.67	lysosomal-associated protein	Laptm4b	NM_033521 // lysosomal-
		transmembrane 4B		associated protein transmembrane 4B
1422052_at	1.67	cadherin 8	Cdh8	NM_007667 // cadherin 8
1456005_a_at	1.67	BCL2-like 11 (apoptosis facilitator)	Bcl2l11	NM_009754 // BCL2-like 11 apoptosis facilitator
1423135_at	1.67	thymus cell antigen 1, theta	Thy1	NM_009382 // thymus cell antigen 1, theta
1439255_s_at	1.67	transmembrane 7 superfamily member 1	Tm7sf1	NM_031999 // transmembrane 7 superfamily member 1
1418506_a_at	1.66	peroxiredoxin 2	Prdx2	NM_011563 // peroxiredoxin 2
1452130_at	1.66	RIKEN cDNA 2310042M24 gene	2310042M24Rik	NM_025868 // RIKEN cDNA 2310042M24
1423796_at	1.66	splicing factor proline/glutamine rich	Sfpq	NM_023603 // splicing factor
		(polypyrimidine tract binding protein		proline/glutamine rich (polypyrimidine tract binding
		associated)		protein associated)
1436912_at	1.66	RIKEN cDNA 3110038O15 gene	3110038O15Rik	NA
1417151_a_at	1.65	neurotensin receptor 2	Ntsr2	NM_008747 // neurotensin receptor 2
1460192_at	1.65	oxysterol binding protein-like 1A	Osbp11a	NM_020573 // oxysterol binding protein-like 1A
1438957_x_at	1.65	CDP-diacylglycerol synthase	Cds2	NM_138651 // phosphatidate cytidylyltransferase 2
		(phosphatidate cytidylyltransferase) 2
1434099_at	1.65	caspase 7	Casp7	NM_007611 // caspase 7
1434256_s_at	1.65	CDP-diacylglycerol synthase	Cds2	NM_138651 // phosphatidate cytidylyltransferase 2
		(phosphatidate cytidylyltransferase) 2
1435614_s_at	1.65	RAS protein-specific guanine nucleotide-	Rasgrf1	NM_011245 // RAS protein-specific
		releasing factor 1		guanine nucleotide-releasing factor 1
1449256_a_at	1.65	RAB11a, member RAS oncogene family	Rab11a	NM_017382 // RAB11a, member RAS oncogene family
1419244_a_at	1.65	RAB14, member RAS oncogene family	Rab14	NM_026697 // RAB14, member RAS oncogene family
1448210_at	1.64	RAB1, member RAS oncogene family	Rab1	NM_008996 // RAB1, member RAS oncogene family
1418073_at	1.64	acyl-Coenzyme A thioesterase 2,	Acate2-pending	NM_019736 // acyl-Coenzyme
		mitochondrial		A thioesterase 2, mitochondrial
1436934_s_at	1.64	aconitase 2, mitochondrial	Aco2	NM_080633 // aconitase 2, mitochondrial
1433562_s_at	1.64	ATP synthase, H+ transporting,	Atp5f1	NM_009725 // ATP synthase,
		mitochondrial F0 complex, subunit b,		H+ transporting, mitochondrial
		isoform 1		F0 complex, subunit b, isoform 1
1426282_at	1.64	neurotrimin	Hnt-pending	NM_172290 // neurotrimin
1455422_x_at	1.64	septin4	38234	NM_011129 // peanut-like 2 homolog
1452141_a_at	1.63	selenoprotein P, plasma, 1	Sepp1	NM_009155 // selenoprotein P, plasma, 1
1437164_x_at	1.63	ATP synthase, H+ transporting,	Atp5o	NM_138597 // ATP synthase,
		mitochondrial F1 complex, O subunit		H+ transporting, mitochondrial F1 complex, O subunit
1428107_at	1.62	SH3-binding domain glutamic acid-rich	Sh3bgrl	NM_019989 // SH3-binding domain
		protein like		glutamic acid-rich protein like
1426917_s_at	1.62	RIKEN cDNA 4833415E20 gene	4833415E20Rik	NA
1423283_at	1.61	phosphatidylinositol transfer protein	Pitpn	NM_008850 // phosphatidylinositol transfer protein
1423079_a_at	1.61	translocase of outer mitochondrial	Tomm20-pending	NM_024214 // translocase of
		membrane 20 homolog (yeast)		outer mitochondrial membrane 20 homolog
1423172_at	1.61	N-ethylmaleimide sensitive fusion protein	Napb	NM_019632 // N-ethylmaleimide sensitive
		attachment protein beta		fusion protein attachment protein beta
1416127_a_at	1.61	aspartyl aminopeptidase	Dnpep	NM_016878 // aspartyl aminopeptidase
1452347_at	1.61	myocyte enhancer factor 2A	Mef2a	NA
1424573_at	1.61	RIKEN cDNA 3110020O18 gene	3110020O18Rik	NM_028445 // /// NM_028876 // CGI-100-like protein
1448237_x_at	1.61	lactate dehydrogenase 2, B chain	Ldh2	NM_008492 // lactate dehydrogenase 2, B chain
1436750_a_at	1.60	3-oxoacid CoA transferase	Oxct	NM_024188 // 3-oxoacid CoA transferase
1417340_at	1.60	thioredoxin-like 2	Txnl2	NM_023140 // thioredoxin-like 2
1424488_a_at	1.60	inorganic pyrophosphatase 2	Sid6306-pending	NM_146141 // inorganic pyrophosphatase 2
1416904_at	1.60	muscleblind-like (Drosophila)	Mbn1	NM_020007 // muscleblind-like
1415753_at	1.60	cDNA sequence BC005632	BC005632	NM_145421 // cDNA sequence BC005632
1417404_at	1.60	ELOVL family member 6, elongation of	Elov16	NM_130450 // ELOVL family member 6,
		long chain fatty acids (yeast)		elongation of long chain fatty acids
1426858_at	1.60	inhibin beta-B	Inhbb	NA
1423399_a_at	1.59	YY1 associated factor 2	Yaf2	NM_024189 // YY1 associated factor 2
1448474_at	1.59	NIMA (never in mitosis gene a)-related	Nek7	NM_021605 // NIMA (never in
		expressed kinase 7		mitosis gene a)-related expressed kinase 7
1419872_at	1.59	colony stimulating factor 1 receptor	Csflr	NM_007779 // colony stimulating factor 1 receptor
1418937_at	1.59	deiodinase, iodothyronine, type II	Dio2	NM_010050 // deiodinase, iodothyronine, type II
1420161_at	1.58	Mus musculus transcribed sequences	NA	NA
1424293_s_at	1.58	RIKEN cDNA 2610319K07 gene	2610319K07Rik	NM_028264 // RIKEN cDNA 2610319K07
1428788_at	1.57	RIKEN cDNA 1700012G19 gene	1700012G19Rik	NM_025954 // RIKEN cDNA 1700012G19
1421022_x_at	1.57	acylphosphatase 1, erythrocyte (common)	Acyp1	NM_025421 //
		type		acylphosphatase 1, erythrocyte (common) type
1422640_at	1.57	protocadherin beta 9	Pcdhb9	NM_053134 // protocadherin beta 9
1416501_at	1.57	3-phosphoinositide dependent protein	Pdpk1	NM_011062 // 3-phosphoinositide
		kinase-1		dependent protein kinase-1
1426312_at	1.57	brain and reproductive organ-expressed	Bre	NM_144541 // brain and reproductive
		protein		organ-expressed protein
1419554_at	1.57	RIKEN cDNA B430305P08 gene	B430305P08Rik	NA
1460180_at	1.56	hexosaminidase B	Hexb	NM_010422 // hexosaminidase B
1451542_at	1.56	single-stranded DNA binding protein 2	Ssbp2	NM_024186 // single-stranded DNA binding
				protein 2 /// NM_024272 // single-stranded
				DNA binding protein 2
1418072_at	1.56	histone 1, H2bc	Hist1h2bc	NM_023422 // histone 1, H2bc
1452152_at	1.56	expressed sequence AI642036	AI642036	NA
1416149_at	1.56	oligodendrocyte transcription factor 1	Olig1	NM_016968 // oligodendrocyte transcription factor 1
1423515_at	1.56	sodium channel, voltage-gated, type VIII,	Scn8a	NM_011323 // sodium channel,
		alpha polypeptide		voltage-gated, type VIII, alpha polypeptide
1418501_a_at	1.56	oxidation resistance 1	Oxr1	NM_130885 // oxidation resistance 1
1451235_at	1.56	BM88 antigen	Bm88-pending	NM_021316 // BM88 antigen
1423978_at	1.55	SH3-binding kinase	Sbk-pending	NM_145587 // SH3-binding kinase
1450757_at	1.55	cadherin 11	Cdh11	NM_009866 // cadherin 11
1450888_at	1.55	brain protein 14	Brp14	NA
1436824_x_at	1.55	ring finger protein 26	Rnf26	NM_153762 // ring finger protein 26
1427182_s_at	1.55	DNA segment, Chr 18, ERATO Doi 653,	D18Ertd653e	NM_172631 // DNA segment,
		expressed		Chr 18, ERATO Doi 653, expressed
1434100_x_at	1.55	caspase 7	Casp7	NM_007611 // caspase 7
1434261_at	1.55	hypothetical protein LOC244668	LOC244668	NA
1425580_a_at	1.55	RIKEN cDNA 5330434F23 gene	5330434F23Rik	NM_181414 // RIKEN cDNA 5330434F23 gene
1425562_s_at	1.55	tRNA nucleotidyl transferase, CCA-	Trnt1	NM_027296 // tRNA nucleotidyl
		adding, 1		transferase, CCA-adding, 1
1416202_at	1.54	B-cell receptor-associated protein 37	Bcap37	NM_007531 // B-cell receptor-associated protein 37
1452202_at	1.54	phosphodiesterase 2A, cGMP-stimulated	Pde2a	NA
1449815_a_at	1.54	single-stranded DNA binding protein 2	Ssbp2	NM_024186 // single-stranded DNA binding
				protein 2 /// NM_024272 // single-stranded DNA binding
				protein 2
1422578_at	1.54	citrate synthase	Cs	NM_026444 // citrate synthase
1421396_at	1.54	proprotein convertase subtilisin/kexin type 1	Pcsk1	NM_013628 // proprotein
1427288_at	1.54	amyloid beta (A4) precursor protein-	Apba2	NA
		binding, family A, member 2		convertase subtilisin/kexin type 1
1423113_a_at	1.54	RIKEN cDNA 1100001F19 gene	1100001F19Rik	NM_025356 // RIKEN cDNA 1100001F19
1456542_s_at	1.53	Mus musculus RIKEN cDNA 2700038P16	NA	NA
		gene, mRNA (cDNA clone
		IMAGE: 4923133), partial cds
1425575_at	1.53	Eph receptor A3	Epha3	NM_010140 // Eph receptor A3
1427470_s_at	1.53	N-ethylmaleimide sensitive fusion protein	Napb	NM_019632 // N-ethylmaleimide sensitive
		attachment protein beta		fusion protein attachment protein beta
1423784_at	1.53	glycyl-tRNA synthetase	Gars	NM_180678 // glycyl-tRNA synthetase
1424885_at	1.53	RIKEN cDNA A630065K24 gene	A630065K24Rik	NM_144810 // RIKEN cDNA A630065K24
1422504_at	1.53	glycine receptor, beta subunit	Glrb	NM_010298 // glycine receptor, beta subunit
1451290_at	1.53	RIKEN cDNA 1010001H21 gene	1010001H21Rik	NM_025735 // RIKEN cDNA 4922501H04
1415918_a_at	1.53	triosephosphate isomerase	Tpi	NM_009415 // triosephosphate isomerase
1429240_at	1.53	StAR-related lipid transfer (START)	Stard4	NM_133774 // StAR-related lipid transfer
		domain containing 4		(START) domain containing 4
1455893_at	1.52	RIKEN cDNA 2610028F08 gene	2610028F08Rik	NM_172815 // RIKEN cDNA 2610028F08
1435659_a_at	1.52	triosephosphate isomerase	Tpi	NM_009415 // triosephosphate isomerase
1424211_at	1.52	RIKEN cDNA 5730438N18 gene	5730438N18Rik	NM_027460 // RIKEN cDNA 5730438N18
1424842_a_at	1.52	RIKEN cDNA 0610025G21 gene	0610025G21Rik	NM_029270 // RIKEN cDNA 0610025G21 ///
				NM_146161 // RIKEN cDNA 0610025G21
1417900_a_at	1.52	very low density lipoprotein receptor	Vldlr	NM_013703 // very low density lipoprotein receptor
1427069_at	1.51	DNA segment, Chr 1, ERATO Doi 578,	D1Ertd578e	NM_175127 // DNA segment, Chr 1, ERATO
		expressed		Doi 578, expressed
1435970_at	1.51	nemo like kinase	Nlk	NM_008702 // nemo like kinase
1416989_at	1.51	RIKEN cDNA 3100002B05 gene	3100002B05Rik	NM_026664 // RIKEN cDNA 3100002B05
1451695_a_at	1.51	glutathione peroxidase 4	Gpx4	NM_008162 // glutathione peroxidase 4
1423736_a_at	1.51	RIKEN cDNA 4933427L07 gene	4933427L07Rik	NM_026986 // /// NM_027727 // RIKEN
				cDNA 4933427L07
1420570_x_at	1.51	T-cell leukemia/lymphoma 1B, 3	Tcl1b3	NM_013772 // T-cell leukemia/lymphoma 1B, 3
1421479_at	1.51	zinc finger protein 318	Zfp318	NM_021346 // zinc finger protein 318
1426994_at	1.51	expressed sequence AI836256	AI836256	NA
1417283_at	1.51	Ly6/neurotoxin 1	Lynx1	NM_011838 // Ly6/neurotoxin 1
1448259_at	1.51	follistatin-like	Fstl	NM_008047 // follistatin-like
1451425_a_at	1.51	makorin, ring finger protein, 1	Mkrn1	NM_018810 // makorin, ring finger protein, 1
1424100_s_at	1.51	BM88 antigen	Bm88-pending	NM_021316 // BM88 antigen
1431074_a_at	1.50	RIKEN cDNA 1110020B03 gene	1110020B03Rik	NM_145823 // retinal degeneration B beta
1451269_at	1.50	RIKEN cDNA 2700099C19 gene	2700099C19Rik	NM_028303 // RIKEN cDNA 2700099C19
1431619_a_at	1.50	dystrobrevin binding protein 1	Dtnbp1	NM_025772 // dystrobrevin binding protein 1
1417892_a_at	1.50	sirtuin 3 (silent mating type information	Sirt3	NM_022433 // sirtuin 3 (silent mating type information
		regulation 2, homolog) 3 (S. cerevisiae)		regulation 2, homolog) 3

TABLE 5
Genes Overexpressed by at Least 1.5 Fold in A10 Cells Relative to A9 Cells
	Fold		UniGene
ID	Induction	UniGene Name	Symbol	Representative mRNA Accession
1415904_at	−17.94	lipoprotein lipase	Lpl	NM_008509 // lipoprotein lipase
1424525_at	−16.19	gastrin releasing peptide	Grp	NM_175012 // gastrin releasing peptide
1422825_at	−6.96	cocaine and amphetamine regulated transcript	Cart-pending	NM_013732 // cocaine and amphetamine
				regulated transcript
1425926_a_at	−6.25	orthodenticle homolog 2 (Drosophila)	Otx2	NM_144841 // orthodenticle homolog 2
1437405_a_at	−5.06	insulin-like growth factor binding protein 4	Igfbp4	NM_010517 // insulin-like growth factor
				binding protein 4
1452004_at	−5.05	calcitonin/calcitonin-related polypeptide, alpha	Calca	NM_007587 // calcitonin/calcitonin-related
				polypeptide, alpha
1423756_s_at	−4.95	insulin-like growth factor binding protein 4	Igfbp4	NM_010517 // insulin-like growth factor
				binding protein 4
1418047_at	−4.71	neurogenic differentiation 6	Neurod6	NM_009717 // neurogenic differentiation 6
1449360_at	−4.71	colony stimulating factor 2 receptor, beta 2,	Csf2rb2	NM_007781 // colony stimulating factor 2
		low-affinity (granulocyte-macrophage)		receptor, beta 2, low-affinity (granulocyte-
				macrophage)
1456307_s_at	−4.12	adenylate cyclase 7	Adcy7	NM_007406 // adenylate cyclase 7
1417065_at	−4.07	early growth response 1	Egr1	NM_007913 // early growth response 1
1426528_at	−3.85	neuropilin 2	Nrp2	NM_010939 // neuropilin 2
1417962_s_at	−3.77	growth hormone receptor	Ghr	NM_010284 // growth hormone receptor
1428664_at	−3.56	vasoactive intestinal polypeptide	Vip	NM_011702 // vasoactive intestinal
				polypeptide
1427509_at	−3.54	RIKEN cDNA 0610007P22 gene	0610007P22Rik	NM_026676 // RIKEN cDNA 0610007P22
1417680_at	−3.52	potassium voltage-gated channel, shaker-related	Kcna5	NM_008419 // potassium voltage-gated
		subfamily, member 5		channel, shaker-related subfamily, member 5
1437029_at	−3.43	tachykinin receptor 3	Tacr3	NM_021382 // neurokinin-3 receptor
1417343_at	−3.37	FXYD domain-containing ion transport regulator 6	Fxyd6	NM_022004 // FXYD domain-containing ion
				transport regulator 6
1428301_at	−3.36	RIKEN cDNA 2610042L04 gene	2610042L04Rik	NM_025940 // RIKEN cDNA 2610042L04
1452731_x_at	−3.34	RIKEN cDNA 2610042L04 gene	2610042L04Rik	NM_025940 // RIKEN cDNA 2610042L04
1417090_at	−3.18	reticulocalbin	Rcn	NM_009037 // reticulocalbin
1418599_at	−3.17	procollagen, type XI, alpha 1	Col11a1	NM_007729 // procollagen, type XI, alpha 1
1417504_at	−3.14	calbindin-28K	Calb1	NM_009788 // calbindin-28K
1436862_at	−3.01	double C2, alpha	Doc2a	NM_010069 // double C2, alpha
1417376_a_at	−2.95	immunoglobulin superfamily, member 4	Igsf4	NM_018770 // immunoglobulin superfamily,
				member 4
1423100_at	−2.95	FBJ osteosarcoma oncogene	Fos	NM_010234 // FBJ osteosarcoma oncogene
1418084_at	−2.94	neuropilin	Nrp	NM_008737 // neuropilin
1420465_s_at	−2.93	major urinary protein 1	Mup1	NM_031188 // major urinary protein 1
1448738_at	−2.88	calbindin-28K	Calb1	NM_009788 // calbindin-28K
1426301_at	−2.85	activated leukocyte cell adhesion molecule	Alcam	NM_009655 // activated leukocyte cell
				adhesion molecule
1435627_x_at	−2.73	MARCKS-like protein	Mlp	NM_010807 // MARCKS-like protein
1437226_x_at	−2.72	MARCKS-like protein	Mlp	NM_010807 // MARCKS-like protein
1425918_at	−2.71	Mus musculus, Similar to EGL nine homolog 3	NA	NA
		(C. elegans), clone MGC: 36685 IMAGE: 5371854,
		mRNA, complete cds
1423427_at	−2.69	adenylate cyclase activating polypeptide 1	Adcyap1	NM_009625 // adenylate cyclase activating
				polypeptide 1
1428379_at	−2.67	solute carrier family 17 (sodium-dependent inorganic	Slc17a6	NM_080853 // solute carrier family 17
		phosphate cotransporter), member 6		(sodium-dependent inorganic phosphate
				cotransporter), member 6
1424586_at	−2.61	DNA sequence AF424697	AF424697	NM_153078 // DNA sequence AF424697
1421595_at	−2.58	NA	NA	NA
1449240_at	−2.58	G substrate	Gsbs-pending	NM_011153 // G substrate
1419406_a_at	−2.57	B-cell CLL/lymphoma 11A (zinc finger protein)	Bcl11a	NM_016707 // B-cell CLL/lymphoma 11A
				(zinc finger protein)
1426208_x_at	−2.56	pleiomorphic adenoma gene-like 1	Plagl1	NM_009538 // pleiomorphic adenoma gene-
				like 1
1435415_x_at	−2.55	MARCKS-like protein	Mlp	NM_010807 // MARCKS-like protein
1451129_at	−2.55	calbindin 2	Calb2	NM_007586 // calbindin 2
1460716_a_at	−2.52	core binding factor beta	Cbfb	NM_022309 // core binding factor beta
1417377_at	−2.47	immunoglobulin superfamily, member 4	Igsf4	NM_018770 // immunoglobulin superfamily,
				member 4
1419077_at	−2.47	membrane protein, palmitoylated 3 (MAGUK p55	Mpp3	NM_007863 // Mpp3 membrane protein,
		subfamily member 3)		palmitoylated 3
1450047_at	−2.43	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	NM_015819 // heparan sulfate 6-O-
				sulfotransferase 2
1418815_at	−2.42	cadherin 2	Cdh2	NM_007664 // cadherin 2
1423760_at	−2.41	CD44 antigen	Cd44	NA
1456108_x_at	−2.41	zinc finger protein 179	Zfp179	NM_009548 // zinc finger protein 179
1448468_a_at	−2.40	potassium voltage-gated channel, shaker-related	Kcnab1	NM_010597 // potassium voltage-gated
		subfamily, beta member 1		channel, shaker-related subfamily, beta
				member 1
1419473_a_at	−2.38	cholecystokinin	Cck	NM_031161 // cholecystokinin
1452406_x_at	−2.37	erythroid differentiation regulator	edr	NM_133362 // erythroid differentiation
				regulator
1423213_at	−2.36	plexin C1	Plxnc1	NM_018797 // plexin C1
1425603_at	−2.29	RIKEN cDNA 0610011I04 gene	0610011I04Rik	NM_025326 // RIKEN cDNA 0610011I04
1421508_at	−2.28	odd Oz/ten-m homolog 1 (Drosophila)	Odz1	NM_011855 // odd Oz/ten-m homolog 1
1448943_at	−2.23	neuropilin	Nrp	NM_008737 // neuropilin
1427917_s_at	−2.22	single-stranded DNA binding protein 3	Ssbp3	NM_023672 // single-stranded DNA-binding
				protein
1418304_at	−2.21	photoreceptor cadherin	Prcad-pending	NM_130878 // photoreceptor cadherin
1448553_at	−2.18	myosin, heavy polypeptide 7, cardiac muscle, beta	Myh7	NM_080728 // myosin, heavy polypeptide 7,
				cardiac muscle, beta
1417378_at	−2.14	immunoglobulin superfamily, member 4	Igsf4	NM_018770 // immunoglobulin superfamily,
				member 4
1418835_at	−2.14	pleckstrin homology-like domain, family A, member 1	Phlda1	NM_009344 // pleckstrin homology-like
				domain, family A, member 1
1415716_a_at	−2.12	ribosomal protein S27	Rps27	NM_027015 // ribosomal protein S27
1418734_at	−2.09	histocompatibility 2, Q region locus 1	H2-Q1	NM_010390 // histocompatibility 2, Q region
				locus 1
1426951_at	−2.08	cysteine-rich motor neuron 1	Crim1	NA
1426002_a_at	−2.08	cell division cycle 7 (S. cerevisiae)	Cdc7	NM_009863 // cell division cycle 7
1450123_at	−2.07	ryanodine receptor 2, cardiac	Ryr2	NM_023868 // ryanodine receptor 2, cardiac
1452035_at	−2.05	procollagen, type IV, alpha 1	Col4a1	NM_009931 // procollagen, type IV, alpha 1
1418603_at	−2.05	arginine vasopressin receptor 1A	Avpr1a	NM_016847 // arginine vasopressin receptor
				1A
1417765_a_at	−2.04	amylase 1, salivary	Amy1	NM_007446 // amylase 1, salivary
1416181_at	−2.03	mesoderm development candiate 2	Mesdc2	NM_023403 // mesoderm development
				candiate 2
1437340_x_at	−2.00	RIKEN cDNA 2200002K21 gene	2200002K21Rik	NM_025466 // RIKEN cDNA 2200002K21
1422710_a_at	−1.99	calcium channel, voltage-dependent, T type, alpha 1H	Cacna1h	NM_021415 // calcium channel alpha13.2
		subunit		subunit
1423415_at	−1.97	G protein-coupled receptor 83	Gpr83	NM_010287 // G protein-coupled receptor
				83
1427600_at	−1.97	Mus musculus 9.5 days embryo parthenogenote cDNA,	NA	NA
		RIKEN full-length enriched library, clone:
		B130041F17
		product: unknown EST, full insert sequence.
AFFX-	−1.96	NA	NA	NA
18SRNAMur/X
00686_M_at
AFFX-	−1.95	NA	NA	NA
18SRNAMur/X
00686_5_at
1452754_at	−1.95	RIKEN cDNA 5730592L21 gene	5730592L21Rik	NM_029720 // RiKEN cDNA 5730592L21
1448812_at	−1.95	hippocalcin-like 1	Hpcal1	NM_016677 // hippocalcin-like 1
1452270_s_at	−1.95	cubilin (intrinsic factor-cobalamin receptor)	Cubn	NA
1418360_at	−1.92	zinc finger protein 179	Zfp179	NM_009548 // zinc finger protein 179
1424051_at	−1.92	procollagen, type IV, alpha 2	Col4a2	NM_009932 // procollagen, type IV, alpha 2
1420377_at	−1.89	sialyltransferase 8 (alpha-2, 8-sialyltransferase) B	Siat8b	NM_009181 // sialyltransferase 8 (alpha-2,
				8-sialyltransferase) B
1426604_at	−1.89	ribonuclease L (2′,5′-oligoisoadenylate synthetase-	Rnasel	NM_011882 // ribonuclease L (2′,5′-
		dependent)		oligoisoadenylate synthetase-dependent)
1428055_at	−1.88	Mus musculus cDNA for MBII-343 snoRNA.	NA	NA
1428074_at	−1.86	RIKEN cDNA 2310037P21 gene	2310037P21Rik	NA
1424547_at	−1.85	carbonic anhydrase 10	Car10	NA
1427320_at	−1.85	coatomer protein complex, subunit gamma 2,	Copg2as2	XR_000142 //
		antisense 2
1437687_x_at	−1.85	FK506 binding protein 9	Fkbp9	NM_012056 // FK506 binding protein 9
1438968_x_at	−1.84	serine protease inhibitor, Kunitz type 2	Spint2	NM_011464 // serine protease inhibitor,
				Kunitz type 2
1435526_at	−1.83	hypothetical protein MGC6357	MGC6357	NM_144791 // hypothetical protein
				MGC6357
1424415_s_at	−1.82	RIKEN cDNA D330035F22 gene	D330035F22Rik	NA
1450905_at	−1.82	plexin C1	Plxnc1	NM_018797 // plexin C1
1429227_x_at	−1.81	nucleosome assembly protein 1-like 1	Nap1l1	NM_015781 // nucleosome assembly protein
				1-like 1
1424214_at	−1.80	RIKEN cDNA 9130213B05 gene	9130213B05Rik	NM_145562 // RIKEN cDNA 9130213B05
1418983_at	−1.80	channel-interacting PDZ domain protein	Cipp	NM_007704 // channel-interacting PDZ
				domain protein /// NM_172696 // channel-
				interacting PDZ domain protein
1448545_at	−1.78	syndecan 2	Sdc2	NM_008304 // syndecan 2
1417011_at	−1.78	syndecan 2	Sdc2	NM_008304 // syndecan 2
1449244_at	−1.77	cadherin 2	Cdh2	NM_007664 // cadherin 2
1425784_a_at	−1.77	olfactomedin 1	Olfm1	NM_019498 // olfactomedin 1
1455177_at	−1.77	Abelson helper integration site	Ahi1	NM_026203 // AHi1
1448554_s_at	−1.76	myosin, heavy polypeptide 7, cardiac muscle, beta	Myh7	NM_080728 // myosin, heavy polypeptide 7,
				cardiac muscle, beta
1418091_at	−1.76	Tcfcp2-related transcriptional repressor 1	Crtr1-pending	NM_023755 // transcription repressor
				CRTR-1
1417782_at	−1.76	RIKEN cDNA 2900019C14 gene	2900019C14Rik	NM_026058 // RIKEN cDNA 2900019C14
1419879_s_at	−1.76	tripartite motif protein 25	Trim25	NA
1452107_s_at	−1.75	nephronectin	Npnt	NM_033525 // nephronectin
1449410_a_at	−1.74	growth arrest specific 5	Gas5	NM_013525 // growth arrest specific 5
1424949_at	−1.74	upstream regulatory element binding protein 1	Ureb1-pending	NA
1427670_a_at	−1.74	transcription factor 12	Tcf12	NM_011544 // transcription factor 12
1426436_at	−1.73	RIKEN cDNA 8430420C20 gene	8430420C20Rik	NM_145586 // promethin
1416997_a_at	−1.73	huntingtin-associated protein 1	Hap1	NM_010404 // huntingtin-associated protein
				1 isoform A /// NM_177981 // huntingtin-
				associated protein 1 isoform B
1418164_at	−1.73	epimorphin	Epim	NM_007941 // epimorphin
1438443_at	−1.72	zinc finger protein 288	Zfp288	NM_019778 // zinc finger protein 288
1423085_at	−1.72	ephrin B3	Efnb3	NM_007911 // ephrin B3
1428875_at	−1.71	RIKEN cDNA 3110027H23 gene	3110027H23Rik	NM_175193 // RIKEN cDNA 3110027H23
1425110_at	−1.71	RIKEN cDNA 6330404A12 gene	6330404A12Rik	NM_025696 // RIKEN cDNA 6330404A12
1449799_s_at	−1.70	RIKEN cDNA 1200008D14 gene	1200008D14Rik	NM_026163 // RIKEN cDNA 1200008D14
				/// NM_027894 //
1421088_at	−1.70	glypican 4	Gpc4	NM_008150 // glypican 4
1417272_at	−1.69	RIKEN cDNA 9130005N14 gene	9130005N14Rik	NM_026667 // RIKEN cDNA 9130005N14
1448065_at	−1.69	UDP-Gal: betaGlcNAc beta 1,4-galactosyltransferase,	B4galt3	NM_020579 // UDP-Gal: betaGlcNAc beta
		polypeptide 3		1,4-galactosyltransferase, polypeptide 3
1417996_at	−1.68	neuroglobin	Ngb	NM_022414 // neuroglobin
1417978_at	−1.68	RIKEN cDNA 1300018P11 gene	1300018P11Rik	NM_025829 // RIKEN cDNA 1300018P11
1424659_at	−1.68	slit homolog 2 (Drosophila)	Slit2	NM_178804 // slit homolog 2
1430195_at	−1.67	RIKEN cDNA 2810043O03 gene	2810043O03Rik	NA
1421340_at	−1.67	mitogen activated protein kinase kinase kinase 5	Map3k5	NM_008580 // mitogen activated protein
				kinase kinase kinase 5
1425314_at	−1.67	monogenic, audiogenic seizure susceptibility 1	Mass1	NM_054053 // monogenic, audiogenic
				seizure susceptibility 1
1423802_at	−1.67	cDNA sequence BC017634	BC017634	NM_145621 // similar to vesicle-associated
				calmodulin-binding protein
1420476_a_at	−1.67	nucleosome assembly protein 1-like 1	Nap1l1	NM_015781 // nucleosome assembly protein
				1-like 1
1455491_at	−1.67	Mus musculus, clone IMAGE: 6741456, mRNA	NA	NA
1422433_s_at	−1.66	isocitrate dehydrogenase 1 (NADP+), soluble	Idh1	NM_010497 // isocitrate dehydrogenase 1
				(NADP+), soluble
1451799_at	−1.66	RIKEN cDNA 2610528H13 gene	2610528H13Rik	NM_145944 // RIKEN cDNA 2610528H13
1418257_at	−1.65	solute carrier family 12, member 7	Slc12a7	NM_011390 // solute carrier family 12,
				member 7
1455628_at	−1.64	RIKEN cDNA 6430543G08 gene	6430543G08Rik	NA
1427501_at	−1.64	hypothetical protein 5031409G23	5031409G23	NA
1422064_a_at	−1.63	zinc finger protein 288	Zfp288	NM_019778 // zinc finger protein 288
1422831_at	−1.63	fibrillin 2	Fbn2	NM_010181 // fibrillin 2
1428113_at	−1.63	RIKEN cDNA 4930403J22 gene	4930403J22Rik	NA
1419638_at	−1.62	ephrin B2	Efnb2	NM_010111 // ephrin B2
1449630_s_at	−1.62	RIKEN cDNA B930025N23 gene	B930025N23Rik	NA
1426774_at	−1.62	expressed sequence AA409132	AA409132	NM_172893 // expressed sequence
				AA409132
1423852_at	−1.60	RIKEN cDNA 9430059P22 gene	9430059P22Rik	NM_145463 // hypothetical protein
				BC024118
1419470_at	−1.60	guanine nucleotide binding protein, beta 4	Gnb4	NM_013531 // guanine nucleotide-binding
				protein, beta-4 subunit
1427123_s_at	−1.60	coatomer protein complex, subunit gamma 2,	Copg2as2	XR_000142 //
		antisense 2
1427156_s_at	−1.60	RIKEN cDNA 1700011I11 gene	1700011I11Rik	NM_029291 // ASC-1 complex subunit P100
1448940_at	−1.59	tripartite motif protein 21	Trim21	NM_009277 // 52 kD Ro/SSA autoantigen
1439260_a_at	−1.59	ectonucleotide pyrophosphatase/phosphodiesterase 3	Enpp3	NA
1417959_at	−1.59	RIKEN cDNA 1110003B01 gene	1110003B01Rik	NM_026131 // RIKEN cDNA 1110003B01
1435184_at	−1.58	RIKEN cDNA B430320C24 gene	B430320C24Rik	NA
1460292_a_at	−1.58	SWI/SNF related, matrix associated, actin dependent	Smarca1	NM_053123 // SWI/SNF related, matrix
		regulator of chromatin, subfamily a, member 1		associated, actin dependent regulator of
				chromatin, subfamily a, member 1
1416111_at	−1.58	CD83 antigen	Cd83	NM_009856 // CD83 antigen
1416874_a_at	−1.58	RIKEN cDNA 5730511K23 gene	5730511K23Rik	NM_019458 // RIKEN cDNA 5730511K23
1455796_x_at	−1.58	olfactomedin 1	Olfm1	NM_019498 // olfactomedin 1
1449236_at	−1.58	delta-like 3 (Drosophila)	Dll3	NM_007866 // delta-like 3 isoform 1
1425264_s_at	−1.57	myelin basic protein	Mbp	NM_010777 // myelin basic protein
1434935_at	−1.57	RIKEN cDNA 5530400K14 gene	5530400K14Rik	NA
1425111_at	−1.57	RIKEN cDNA 6330404A12 gene	6330404A12Rik	NM_025696 // RIKEN cDNA 6330404A12
1422629_s_at	−1.57	shroom	Shrm	NM_015756 // shroom
1436921_at	−1.55	ATPase, Cu++ transporting, alpha polypeptide	Atp7a	NM_009726 // ATPase, Cu++ transporting,
				alpha polypeptide
1419254_at	−1.55	methylenetetrahydrofolate dehydrogenase (NAD+	Mthfd2	NM_008638 // methylenetetrahydrofolate
		dependent), methenyltetrahydrofolate cyclohydrolase		dehydrogenase (NAD+ dependent),
				methenyltetrahydrofolate cyclohydrolase
1418774_a_at	−1.55	ATPase, Cu++ transporting, alpha polypeptide	Atp7a	NM_009726 // ATPase, Cu++ transporting,
				alpha polypeptide
1415691_at	−1.55	discs, large homolog 1 (Drosophila)	Dlgh1	NM_007862 // discs large homolog 1
1420342_at	−1.54	ganglioside-induced differentiation-associated-protein	Gdap10	NM_010268 // ganglioside-induced
		10		differentiation-associated-protein 10
1423489_at	−1.54	monocyte to macrophage differentiation-associated	Mmd	NM_026178 // monocyte to macrophage
				differentiation-associated
1423851_a_at	−1.54	RIKEN cDNA 9430059P22 gene	9430059P22Rik	NM_145463 // hypothetical protein
				BC024118
1455222_a_at	−1.54	upstream binding protein 1	Ubp1	NM_013699 // upstream binding protein 1
1427052_at	−1.54	acetyl-Coenzyme A carboxylase beta	Acacb	NA
1416807_at	−1.54	ribosomal protein L44	Rpl44	NM_019865 // ribosomal protein L44
1453037_at	−1.53	RIKEN cDNA 1110002E23 gene	1110002E23Rik	NM_025365 // RIKEN cDNA 1110002E23
1417220_at	−1.53	fumarylacetoacetate hydrolase	Fah	NM_010176 // fumarylacetoacetate
				hydrolase
1449315_at	−1.53	odd Oz/ten-m homolog 3 (Drosophila)	Odz3	NM_011857 // odd Oz/ten-m homolog 3
1439244_a_at	−1.53	hypothetical protein MGC11932	MGC11932	NM_144925 // hypothetical protein
				MGC11932
1460324_at	−1.53	Mus musculus transcribed sequences	NA	NA
1452222_at	−1.53	utrophin	Utrn	NM_011682 // utrophin
1416301_a_at	−1.53	early B-cell factor 1	Ebf1	NM_007897 // early B-cell factor 1
1419291_x_at	−1.52	growth arrest specific 5	Gas5	NM_013525 // growth arrest specific 5
1427795_s_at	−1.52	Mus musculus, clone IMAGE: 6494162, mRNA	NA	NA
1419655_at	−1.52	transducin-like enhancer of split 3, homolog of	Tle3	NM_009389 // transducin-like enhancer
		Drosophila E(spl)		protein 3
1454789_x_at	−1.52	RIKEN cDNA 2610031L17 gene	2610031L17Rik	NM_133701 // RIKEN cDNA 1190003A07
1419186_a_at	−1.51	sialyltransferase 8 (alpha-2, 8-sialyltransferase) D	Siat8d	NM_009183 // sialyltransferase 8 (alpha-2,
				8-sialyltransferase) D
1451501_a_at	−1.51	growth hormone receptor	Ghr	NM_010284 // growth hormone receptor
1423437_at	−1.51	glutathione S-transferase, alpha 3	Gsta3	NM_010356 // glutathione S-transferase,
				alpha 3
1427254_at	−1.51	expressed sequence AW610627	AW610627	NM_173364 // expressed sequence
				AW610627
1423404_at	−1.51	RIKEN cDNA 2200002K21 gene	2200002K21Rik	NM_025466 // RIKEN cDNA 2200002K21
1460637_s_at	−1.51	prefoldin 5	Pfdn5	NM_020031 // prefoldin 5
1422834_at	−1.51	potassium voltage-gated channel, Shal-related family,	Kcnd2	NM_019697 // potassium voltage-gated
		member 2		channel, Shal-related family, member 2
1424632_a_at	−1.51	REV3-like, catalytic subunit of DNA polymerase zeta	Rev3l	NM_011264 // REV3-like, catalytic subunit
		RAD54 like (S. cerevisiae)		of DNA polymerase zeta RAD54 like
1417022_at	−1.51	solute carrier family 7 (cationic amino acid transporter,	Slc7a3	NM_007515 // solute carrier family 7
		y+ system), member 3		(cationic amino acid transporter, y+ system),
				member 3
1418004_a_at	−1.50	RIKEN cDNA 1810009M01 gene	1810009M01Rik	NM_023056 // LR8 protein
1449106_at	−1.50	glutathione peroxidase 3	Gpx3	NM_008161 // glutathione peroxidase 3
1448925_at	−1.50	twist homolog 2 (Drosophila)	Twist2	NM_007855 // twist homolog 2
1438802_at	−1.50	forkhead box P1	Foxp1	NM_053202 // forkhead box P1
1419967_at	−1.50	sec13-like protein	Sec13l-pending	NM_028112 // sec13-like protein

Other Embodiments

All publications and patent applications cited in this specification are herein incorporated by reference as if each individual publication or patent application were specifically and individually indicated to be incorporated by reference. Although the foregoing invention has been described in some detail by way of illustration and example for-purposes of clarity of understanding, it will be readily apparent to those of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.

Claims

1. A method of identifying a compound for treating or preventing Parkinson's disease, said method comprising the steps of: (a) providing cells that express at least five genes selected from Table 4; (b) contacting said cells with a candidate compound; and (c) assessing the expression level of said genes relative to the expression level of said genes in the absence of said candidate compound, wherein a candidate compound that reduces the expression of at least three of said genes is identified as a compound useful for treating or preventing Parkinson's disease.

2. The method of claim 1, wherein said cells comprise more than one cell-type.

3. The method of claim 1, wherein all of said genes are expressed in a single cell-type.

4. The method of claim 1, wherein said cells express at least 10 genes selected from Table 4.

5. The method of claim 1, wherein said cells express at least 50 genes selected from Table 4.

6. The method of claim 2, wherein said each cell-type is segregated from the other cell-types during steps (b) and (c).

7. The method of claim 1, wherein said contacting further comprises contacting said cell with a mitochondrial complex I inhibitor.

8. The method of claim 7, wherein said mitochondrial complex I inhibitor is 1-methyl-4-phenylpyridinium (MPP+), rotenone, isoquinoline, tetrahydroisoquinoline, or 6-hydroxydopamine.

9. The method of claim 1, wherein said cells are mammalian cells.

10. The method of claim 9, wherein said cell is a human cell or a rodent cell.

11. The method of claim 10, wherein at least one of said cells is a dopaminergic cell or a cell isolated from the ventral mesencephalic tissue.

12. The method of claim 1, wherein at least one of said cells is a PC12 cell.

13. The method of claim 12, wherein said PC12 cells overexpress α-synuclein.

14. The method of claim 1, wherein said assessing step (c) comprises measuring the RNA levels transcribed from said gene.

15. The method of claim 1, wherein said assessing step (c) comprises measuring the amount of said protein encoded by said gene.

16. The method of claim 1, wherein at least one of said genes is recombinantly expressed by said cells.

17. A method of identifying a compound for treating or preventing Parkinson's disease, said method comprising the steps of: (a) providing cells that expresses at least five genes selected from Table 5; (b) contacting said cells with a candidate compound; and (c) assessing the expression level of said genes relative to the expression level of said protein in the absence of said candidate compound, wherein a candidate compound that increases the expression of at least three of said genes is identified as a compound useful for treating or preventing Parkinson's disease.

18. The method of claim 17, wherein said cells comprise more than one cell-type.

19. The method of claim 17, wherein all of said genes are expressed in a single cell-type.

20. The method of claim 17, wherein said cells express at least 10 genes selected from Table 5.

21. The method of claim 17, wherein said cells express at least 50 genes selected from Table 5.

22. The method of claim 18, wherein said each cell-type is segregated from the other cell-types during steps (b) and (c).

23. The method of claim 17, wherein said contacting further comprises contacting said cell with a mitochondrial complex I inhibitor.

24. The method of claim 23, wherein said mitochondrial complex I inhibitor is 1-methyl-4-phenylpyridinium (MPP+), rotenone, isoquinoline, tetrahydroisoquinoline, or 6-hydroxydopamine.

25. The method of claim 17, wherein said cells are mammalian cells.

26. The method of claim 25, wherein said cell is a human cell or a rodent cell.

27. The method of claim 26, wherein at least one of said cells is a dopaminergic cell or a cell isolated from the ventral mesencephalic tissue.

28. The method of claim 17, wherein at least one of said cells is a PC12 cell.

29. The method of claim 28, wherein said PC12 cells overexpress α-synuclein.

30. The method of claim 17, wherein said assessing step (c) comprises measuring the RNA levels transcribed from said gene.

31. The method of claim 17, wherein said assessing step (c) comprises measuring the amount of said protein encoded by said gene.

32. The method of claim 17, wherein at least one of said genes is recombinantly expressed by said cells.

33. A method of identifying a compound for treating or preventing Parkinson's disease, said method comprising the steps of: (a) providing a cell comprising a reporter gene operably linked to the promoter of a gene selected from Table 4; (b) contacting said cell with a candidate compound; and (c) assessing the level of expression of said reporter gene relative to the level of expression of said reporter gene in the absence of said candidate compound, wherein a candidate compound that reduces the level of expression of said reporter gene is identified as a compound that is useful for the treatment or prevention of Parkinson's disease.

34. The method of claim 33, wherein said reporter gene is selected from the group consisting of glucuronidase (GUS), luciferase, chloramphenicol transacetylase (CAT), green fluorescent protein (GFP), alkaline phosphatase, and β-galactosidase.

35. The method of claim 33, wherein said contacting further comprises contacting said cell with a mitochondrial complex I inhibitor.

36. The method of claim 35, wherein said mitochondrial complex I inhibitor is 1-methyl-4-phenylpyridinium (MPP+), rotenone, isoquinoline, or tetrahydroisoquinoline.

37. The method of claim 36, wherein said cell is a human cell or a rodent cell.

38. The method of claim 33, wherein said cell is a dopaminergic cell or a cell isolated from the ventral mesencephalic tissue.

39. The method of claim 33, wherein said cell is a PC12 cell.

40. The method of claim 39, wherein said PC12 cell overexpresses α-synuclein.

41. A method of identifying a compound for treating or preventing Parkinson's disease, said method comprising the steps of: (a) providing a cell comprising a reporter gene operably linked to the promoter of a gene selected from Table 5; (b) contacting said cell with a candidate compound; and (c) assessing the level of expression of said reporter gene relative to the level of expression of said reporter gene in the absence of said candidate compound, wherein a candidate compound that increases the level of expression of said reporter gene is identified as a compound that is useful for the treatment or prevention of Parkinson's disease.

42. The method of claim 41, wherein said reporter gene is selected from the group consisting of glucuronidase (GUS), luciferase, chloramphenicol transacetylase (CAT), green fluorescent protein (GFP), alkaline phosphatase, and β-galactosidase.

43. The method of claim 41, wherein said contacting further comprises contacting said cell with a mitochondrial complex I inhibitor.

44. The method of claim 43, wherein said mitochondrial complex I inhibitor is 1-methyl-4-phenylpyridinium (MPP+), rotenone, isoquinoline, or tetrahydroisoquinoline.

45. The method of claim 41, wherein said cell is a mammalian cell.

46. The method of claim 45, wherein said cell is a human cell or a rodent cell.

47. The method of claim 41, wherein said cell is a dopaminergic cell or a cell isolated from the ventral mesencephalic tissue.

48. The method of claim 41, wherein said cell is a PC12 cell.

49. The method of claim 48, wherein said PC12 cell overexpresses α-synuclein.

50. A solid support surface comprising 1000 or fewer unique polynucleotide probes capable of binding at least 200 distinct nucleic acids that encode the genes of Table 4 and Table 5, wherein said probes are arranged on said surface such that, when contacted with a sample containing said nucleic acids, each binding event is segregated from the others.

51. The solid support surface of claim 50, wherein said 1000 or fewer unique polynucleotide probes capable of binding at least 300 distinct nucleic acids that encode the genes of Table 4 and Table 5.

52. The solid support surface of claim 50, wherein said 1000 or fewer distinct polynucleotide probes capable of binding at least 400 distinct nucleic acids that encode the genes of Table 4 and Table 5.

53. The solid support surface of claim 50, wherein said polynucleotide probes are conjugated to a detectable label.

54. The solid support surface of claim 53, wherein said detectable label is a fluorescent label or an enzyme tag.

55. The solid support surface of claim 54, wherein said enzyme tag is selected from the group consisting of digoxigenin, β-galactosidase, urease, alkaline phosphatase, peroxidase, or avidin/biotin complex.

56. The surface of claim 55, wherein said surface is a multiwell plate.

57. The surface of claim 55, wherein said surface is a slide.