Patent Application
20130018083
The present invention concerns Sipa1I1 a new target involved in adipogenesis modulation as well as screening test for identification of modulators of the activity of this target. Further, the present invention relates to modulators of Sipa1I1 activity and their use, especially in pharmaceutical composition, to modulate adipogenesis and thus treat obesity and related disorders.
Obesity is a major risk factor for a number of disorders including hypertension, coronary artery disease, dyslipidemia, insulin resistance and type 2 diabetes. Because of the importance of the obesity epidemic, a great deal of investigation has centered on the biology of the adipocyte, including the developmental pathway by which new adipocytes are created. Adipogenesis is the process by which undifferentiated mesenchymal precursor cells become mature adipocytes. Throughout the last decade considerable progress has been made in elucidating the molecular mechanisms of adipocyte differentiation, which involve sequential activation of transcription factors from several families such as CCAAT/enhancer binding proteins (C/EBPα, α, and γ) and the nuclear hormone receptor peroxisome proliferator-activated receptor γ (PPARγ) (Rosen, E. D. et al., 2002). PPARγ is described as a “master regulator” of adipogenesis since it has been shown to be both sufficient and necessary for adipogenesis both in vitro and in vivo. Recently, new transcription factors have been described to participate in adipogenesis such as KLF family (KLF2, 5 and KLF15) (Banerjee, S. S. et al., 2003; Gray, S. M. et al., 2002), Ebf family (Jimenez, M. A. et al., 2007) and Krox 20 (Chen, Z. et al., 2005), suggesting that the transcriptional cascade occurring during adipogenesis is much more complex than previously thought. Furthermore, signaling molecules and/or receptors such as the Wnt family of secreted proteins (Kang S. et al., 2007), sonic hedgehog protein, Notch receptor have also been described to be involved in molecular events leading to adipocyte formation. It is interesting to note that extracellular and intracellular events are somehow coupled to regulate adipogenesis. All these signaling pathways converge on a tightly regulated transcriptional cascade, which needs to be more completely understood to potentially control adipocyte development and prevent obesity.
Storage of fat in adipose tissue is limited and exceeding this capacity leads to accumulation of lipids in others tissues, in particular muscle, liver, and the endocrine pancreas, and to the secretion by adipocytes of various adipokines. The adipose tissue consists of several deposits located at different anatomical sites which may originate from distinct precursors and which have different physiological functions and pathophysiological roles. The visceral, as opposed to the subcutaneous adipose depots, may contribute more to the defects associated with the metabolic syndrome.
Cannabinoid 1 receptors have been identified in all organs playing a key role in glucose metabolism and type 2 diabetes, i.e. adipose tissue, the gastrointestinal tract, the liver, the skeletal muscle and the pancreas. Rimonabant, the first selective cannabinoid receptor 1 (CB1R) antagonist in clinical use, has been shown to reduce food intake and body weight thus improving glucose metabolism regulation.
However, there is still a need for novel therapeutic targets for the treatment of obesity.
Spa1 mouse protein is known to hamper mitogen-induced cell cycle progression when abnormally or prematurely expressed. The human Sipa1 gene was cloned in 1997; it encodes a 1042-amino acid polypeptide with a predicted mass of 130 kD. The protein contains a C-terminal leucine zipper motif and an N-terminal GTPase activating protein (GAP) domain homologous to the human RAP1GAP protein (Tsai, I. C. et al., 2007). Human and mouse Spa1 amino acid sequences are 90% identical, with their GAP domains 98% identical. Human SPA1 was expressed at high levels in lymphohematopoietic tissues and at lower levels in several other tissues. Sipa1I1 belongs to the Rap/Ras GTPase activating protein family and has been described as an anti-apoptotic protein by acting on p53 expression. This protein has a PDZ domain and can potentially bind to transcription factors and modulate their action on gene transcription.
The inventors have now found that Sipa1I1 plays a critical role in adipocyte differentiation. Sipa1I1 might modify gene expression by acting on cofactors or intermediate signaling proteins. It is a now considered as a new relevant target for modulation of adipogenesis, and thus for the treatment of obesity and related disorders.
The present invention consists in the use of inhibitors of Sipa1I1 activity for modulation of adipogenesis, in particular for treatment of obesity and related disorders. The invention also concerns pharmaceutical composition containing such modulators of adipogenesis and related disorders and screening test for such modulators.
There is a need for new therapeutical targets useful to regulate adipogenesis and to treat obesity and related disorders. The inventors have now identified le role of Sipa1I1 in adipogenesis modulation.
Through a transcriptomic approach, they identified genes whose expression was correlated with body weight gain in cohorts of C57BI/6 mice fed a high fat diet. Then, they conducted a second analysis in order to evaluate the changes in gene expression induced by rimonabant treatment of the high fat diet fed mice. Genes which have never been described before in adipocyte biology, but which might be involved in important biological processes such as signaling, modification of extracellular matrix proteins, and gene transcription were retained. These genes could be important for adipogenesis especially since they might be involved in the mechanism by which rimonabant reduces fat mass in mice. In this context, Sipa1I1 was identified as involved in adipocytes metabolism, especially in new signaling pathway. More generally, this gene appears to play a role in adipogenesis and control of adipose tissue development in obesity.
The present invention consists in identification of modulators of Sipa1I1 activity. Such modulators can be any compound or molecule able to modulate Sipa1I1 activity in particular small molecules, lipids and siRNA.
Modulators of Sipa1I1 activity can be identified by detecting the ability of an agent to modulate the activity of Sipa1I1. Inhibitors of Sipa1I1 are any compound able to reduce or inhibit, totally or partially, the activity of Sipa1I1. Inhibitors of Sipa1I1 include, but are not limited to, agents that interfere with the interaction of Sipa1I1 with its natural ligand in the intracellular compartment, agents that reduce Sipa1I1 expression, both at transcriptional and translational levels, as well as agents that inhibit intracellular signals wherein Sipa1I1 is involved.
In one embodiment, Sipa1I1 activity can be reduced using small molecules that inhibit, totally or partially, the transcription of Sipa1I1. Such modulators can be identified using methods well known by the person skilled of the art, as a reporting system consisting in the promoter of Sipa1I1 linked in frame to a reporter gene and expressed in a suitable cell line; the reporter gene product's activity can be quantitatively measured. Thus, a compound that inhibits the expression of the reporter gene, for example by inhibiting an activating transcription factor, can be considered as a potential candidate.
The reporter genes that can be used in such reporting systems are numerous and well known in the art. For example, such reporter genes can be genes allowing expression of Green Fluorescent Protein (GFP), luciferase, β-galactosidase . . . .
Therefore, on aspect of the present invention is to provide a method for screening for inhibitors of the activity of Sipa1I1 which comprises the steps of:
a) transfecting a cell line with a reporter construction comprising a Sipa1I1 promoter linked to a reporter gene,
b) cultivating said cell line in condition to allow expression of the reporter gene,
c) adding candidate compounds into the cell culture,
d) identifying inhibitor compounds as being those compounds which have the ability to reduce or inhibit the reporter gene expression.
The predicted promoter of Sipa1I1 to be used in the described above screening test for modulators of Sipa1I1 transcription corresponds to SEQ ID NO. 19.
In another embodiment, the expression of Sipa1I1 is modulated through RNA interference, using small interfering RNAs (siRNA) or small hairpin RNAs (shRNAs). Therefore, in one aspect, the present invention relates to double stranded nucleic acid molecules including small nucleic acid molecules, such as short interfering nucleic acid (siNA), short interfering RNA (siRNA), double-stranded RNA (dsRNA), micro-RNA (miRNA), and short hairpin RNA (shRNA) molecules able to mediate RNA interference (RNAi) against Sipa1I1 gene expression, including cocktails of such small nucleic acid molecules and suitable formulations of such small nucleic acid molecules.
The phenomenon of RNAi mediated gene silencing has been described first in the Caenorhabditis elegans system, in which microinjection of long double stranded RNA molecules was reported. The mechanism of RNA mediated gene inactivation seems to be slightly different in the various organisms that have been investigated so far. However, in all systems, RNA mediated gene silencing is based on post-transcriptional degradation of the target mRNA induced by the endonuclease Argonaute2 which is part of the so called RISC complex. Sequence specificity of degradation is determined by the nucleotide sequence of the specific antisense RNA strand loaded into the RISC complex.
The introduction into cells of a siRNA compound results in cells having a reduced level of the target mRNA and, thus, of the corresponding polypeptide and, concurrently, of the corresponding enzyme activity.
SiRNAs specific for Sipa1I1, as described herein, can be used as modulators of Sipa1I1 activity, in order to reduce the translation of Sipa1I1 mRNA. More particularly, siRNA specific for Sipa1I1 can be used to reduce adipogenesis and thus to treat obesity and related diseases.
In one embodiment, the invention features a double stranded nucleic acid molecule, such as an siRNA molecule, where one of the strands comprises nucleotide sequence having complementarity to a predetermined Sipa1I1 nucleotide sequence in a target Sipa1I1 nucleic acid molecule, or a portion thereof.
The RNA molecule can be used modified or unmodified. An example of modification is the incorporation of tricylo-DNA to allow improved serum stability of oligonucleotide.
In one embodiment, the predetermined Sipa1I1 nucleotide sequence is a Sipa1I1 nucleotide target sequence described herein (SEQ ID NO. 1 and SEQ ID NO. 3).
Due to the potential for sequence variability of the genome across different organisms or different subjects, selection of siRNA molecules for broad therapeutic applications likely involves the conserved regions of the gene. Thus in one embodiment, the present invention relates to siRNA molecules that target conserved regions of the genome or regions that are conserved across different targets. SiRNA molecules designed to target conserved regions of various targets enable efficient inhibition of Sipa1I1 gene expression in diverse patient populations.
In one embodiment, the invention features a double-stranded short interfering nucleic acid molecule that down-regulates expression of a target Sipa1I1 gene or that directs cleavage of a target RNA, wherein said siRNA molecule comprises about 15 to about 28 base pairs, preferably 19 base pairs. A siRNA or RNAi inhibitor of the instant invention can be chemically synthesized, expressed from a vector or enzymatically synthesized.
In a particular embodiment, the siRNA specific for Sipa1I1 are shRNA having sequence SEQ ID NO. 5 or SEQ ID NO. 6. In a preferred embodiment, the siRNA specific for Sipa1I1 is shRNA having sequence SEQ ID NO. 6.
The use of a siRNA according to the present invention leads to reduction of the mRNA level from 5% to 20%, preferably from 5% to 15%, more preferably from 5% to 10% of the mRNA level of the corresponding wild type cell. The wild type cell is the cell prior to the introduction of the nucleic acid encoding the siRNA compound, in which the targeted mRNA is not degraded by a siRNA compound.
Inhibitors of Sipa1I1 activity can be administrated by any suitable route, both locally or systemically depending on the nature of the molecule and the expected effect. SiRNA can be administrated locally in case of double strand molecule directly in the targeted tissue, or administrated through a vector in case of shRNA, according to protocols used in the art.
In one embodiment, RNAi is obtained using shRNA molecules. ShRNA constructs encode a stem-loop RNA. After introduction into cells, this stem-loop RNA is processed into a double stranded RNA compound, the sequence of which corresponds to the stem of the original RNA molecule. Such double stranded RNA can be prepared according to any method known in the art including in vitro and in vivo methods as, but not limited to, described in Sahber et al (1987), Bhattacharyya et al, (1990) or U.S. Pat. No. 5,795,715.
For in vivo administration, shRNA can be introduced into a plasmid. Plasmid-derived shRNAs present the advantage to provide the option for combination with reporter genes or selection markers, and delivery via viral or non viral vectors. The introduction of shRNA into a vector and then into cells ensure that the shRNA is continuously expressed. The vector is usually passed on to daughter cells, allowing the gene silencing to be inherited.
The present invention also provides vectors comprising the polynucleotides for expression of shRNA expression of the invention. These vectors are for example AAV vector, retroviral vector in particular lentiviral vector, adenoviral vector which can be administered by different suitable routes including intravenous route, intramuscular route, direct injection into subcutaneous tissue or other targeted tissue chosen according to usual practice.
The route of administration of siRNA varies from local, direct delivery to systemic intravenous administration. The advantage of local delivery is that the doses of siRNA required for efficacy are substantially low since the molecules are injected into or near the target tissue. Local administration also allows for focused delivery of siRNA. For such direct delivery, naked siRNA can be used. “Naked siRNA” refers to delivery of siRNA (unmodified or modified) in saline or other simple excipients such as 5% dextrose. The ease of formulation and administration of such molecules makes this an attractive therapeutic approach. Naked DNA can also be formulated into lipids especially liposomes.
Systemic application of siRNA is often less invasive and, more importantly, not limited to tissues which are sufficiently accessible from outside. For systemic delivery, siRNA can be formulated with cholesterol conjugate, liposomes or polymer-based nanoparticles. Liposomes are traditionally used in order to provide increased pharmacokinetics properties and/or decreased toxicity profiles. They allow significant and repeated success in vivo delivery. Currently, use of lipid-based formulations of systemic delivery of siRNA, especially to hepatocytes, appears to represent one of the most promising near-term opportunities for development of RNAi therapeutics. Formulation with polymers such as dynamic polyconjugates—for example coupled to N-acetylglucosamine for hepatocytes targeting—and cyclodextrin-based nanoparticles allow both targeted delivery and endosomal escape mechanisms. Others polymers such as atelocollagen and chitosan allow therapeutic effects on subcutaneous tumor xenografts as well as on bone metastases.
SiRNA can also be directly conjugated with a molecular entity designed to help targeted delivery. Given the nature of the siRNA duplex, the presence of the inactive or sense stand makes for an ideal site for conjugation. Examples of conjugates are lipophilic conjugates such as cholesterol, or aptamer-based conjugates.
Cationic peptides and proteins are also used to form complexes with the negatively charged phosphate backbone of the siRNA duplex.
These different delivery approaches can be used to target the Sipa1I1 siRNA into the relevant tissue, especially adipose tissue. For such targeting, siRNA can be conjugated to different molecules interacting with pre-adipocytes and adipocytes, as for example ligands interacting with lipids transporters, receptors, insulin receptor or any molecule known in the art.
Another object of the invention is a pharmaceutical composition, which comprises, as active principle, a modulator of Sipa1I1 according to the present invention. These pharmaceutical compositions comprise an effective dose of at least one modulator according to the invention, and at least one pharmaceutically acceptable excipient. Said excipients are chosen according to the pharmaceutical form and the administration route desired, among usual excipients known of one of skill in the art.
The invention also consists in a method for modulation of adipogenesis. Such method can be used to treat obesity or related diseases. Such method can also be used in order to decrease fat accumulation in a cosmetic purpose.
Modulators of Sipa1I1 activity are useful in therapeutics to modulate adipogenesis, in particular in the treatment and prevention of obesity related disorders, in particular type 2 diabetes, dyslipidemia, elevated blood pressure, insulin resistance, cardiovascular disorders and more generally metabolic syndromes.
The present invention, according to another of its aspects, relates to a method for the treatment of the above pathologies, which comprises the in vivo administration to a patient of an effective dose of a modulator of Sipa1I1 according to the invention.
The appropriate unitary dosage forms comprise the oral forms, such as tablets, hard or soft gelatin capsules, powders, granules and oral solutions or suspensions, the sublingual, buccal, intratracheal, intraocular, intranasal forms, by inhalation, the topical, transdermal, sub-cutaneous, intramuscular or intra-venous forms, the rectal forms and the implants. For the topical application, the compounds of the invention may be used as creams, gels, ointments or lotions.
According to usual practice, the dosage suitable to each patient is determined by the physician according to the administration route, the weight and response of the patient.
Sipa1I1 inhibitors are also useful for cosmetic applications in order to reduce disgraceful fat accumulation. For cosmetic applications, inhibitors of Sipa1I1 can be incorporated in a suitable formulation for topical use. The inhibitors of Sipa1I1 can both be small molecules or siRNA as previously described.
The invention is now described by reference to the following examples, which are illustrative only, and are not intended to limit the present invention.
C57BL/6J mice, which are obesity-prone (Collins S. et al., 2004) were fed for 6 months with a high fat diet (HFD). After 6 months of HFD, mice exhibited scattered body weights with various degrees of glucose intolerance (measured by a glucose tolerance test. The HFD mice were separated into 3 groups displaying the same level of glucose intolerance but with low (L), medium (M) or high (H) body weights and treated them, as well as normal chow (NC) fed mice, for one month with vehicle or Rimonabant (10 mg.kg−1.day−1), to normalize their body weight. The treatment also normalized glucose tolerance, as described previously (Poirier et al., 2005).
RNA Preparation, Labelling and Hybridization on cDNA Microarrays.
RNA from 5 different mice per group was extracted from visceral and subcutaneous adipose tissues using peqGOLD Trifast™ (peqlab) and chloroform-isoamylalcool (24:1) extraction. RNA was precipitated with isopropanol and purified by passage over RNeasy columns (Qiagen). RNA quality was checked before and after amplification with a Bioanalyzer 2100 (Agilent). RNA was reverse transcribed and RNA was amplified with MessageAmp™ kit (Ambion). A Mouse Universal Reference (Clontech) was similarly amplified and both adipose tissue and reference RNAs were labeled by an indirect technique with Cy5 and Cy3 according to published protocols (de Fourmestraux et al., J. Biol. Chem. 2004 279:50743-53). Labeled RNAs were hybridized to microarrays containing 17664 cDNAs prepared at the DNA Array Facility of the University of Lausanne. Scanning, image, and quality control analyses were performed as previously published (de Fourmestraux et al., J. Biol. Chem. 2004 279:50743-53). Data were expressed as log2 intensity ratios (Cy5/Cy3), normalized with a print tip locally weighted linear regression (Lowess) method and filtered based on spot quality and incomplete annotation. All analyses were performed with the R software for statistical computing available at the Comprehensive R Archive Network (cran.us.r-project.org/).
3T3-L1 cells were cultured in DMEM (Gibco) with 10% FBS (Gibco) at 5% CO2. After retroviral infection (see below), cells were allow to grow to confluence in either 100-mm or 60-mm dishes in DMEM with 10% FBS. Once confluence was reached, cells were exposed to differentiation medium containing dexamethasone (1 μM), insulin (5 μg/ml), and isobutylmethylxanthine (0.5 μM) (DMI). After 2 days cells were maintained in medium containing insulin (5 μg/ml) until ready for harvest at 7 days.
After 7 to 10 days of differentiation, cells were washed once in PBS and fixed with formaldehyde (Formalde-fresh; Fisher) for 15 minutes. The staining solution was prepared by dissolving 0.5 g oil-red-O in 100 ml of isopropanol; 60 ml of this solution was mixed with 40 ml of distilled water. After 1 hour at room temperature the staining solution was filtered and added to dishes for 4 hours. The staining solution was then removed and cells were washed twice with distilled water.
shRNA Constructs
ShRNAs were constructed using the RNAi-Ready pSIREN-RetroQ ZsGreen (Clontech). Target sequences for Sipa1I1 were designed by querying the Whitehead siRNA algorithm (http://jura.wi.mit.edu/bioc/siRNAext/) as well as the siRNA designer software from Clontech (http://bioinfo.clontech.com/rnaidesigner/); at least two sequences represented by both algorithms were subcloned into the pSIREN vectors (Clontech) using the EcoRI and BamH1 restriction sites. The following target sequences for Sipa1I1 were chosen SEQ ID NO. 18. As a negative control, we used the following siRNA sequence against luciferase: SEQ ID NO. 7.
Transfection of shRNA Constructs
The specificity of shRNAs was tested in 293T HEK cells co-transfected using calcium-Phosphate methods described in Jordan M. et al (2004) with expression vectors containing Sipa1I1 cDNA and the RNAi-Ready pSIREN-RetroQ ZsGreen vector expressing either the shRNA against lucifeare (control shLUC) or Sipa1I1. RT-PCR analysis was performed on cell RNA-extraction 24 h after transfection.
Retroviruses were constructed in the RNAi-Ready pSIREN-RetroQ ZsGreen (pSIREN Clontech) or pMSCV puromycin plasmid (pMSCV, Clontech). Viral constructs were transfected using calcium-phosphate method described in Jordan M. et al (2004) into 293 HEK packaging cells along with constructs encoding gag-pol and the VSV-G protein. Supernatants were harvested after 48 h in presence of 3 pm of Trichostatin A (Sigma) and either used immediately or snap frozen and stored at −80° C. for later use. Viral supernatants were added to the cells for 6 hours in the presence of polybrene (4 μg/ml) and diluted two times with fresh medium for the next 15 hours.
Isolation of Adipocytes and Stromal Vascular Fraction (SVF) from Adipose Tissue
Eight week-old male C57BL/6J mice (n=6-8) were euthanized by CO2 inhalation and epididymal (visceral) and subcutaneous adipose tissue were collected and placed in DMEM medium containing 10 mg/mL fatty acid-poor BSA (Sigma-Aldrich, St. Louis, Mich.). The tissue was minced into fine pieces and then digested in 0.12 units/mL collagenase type I (Sigma) at 37° C. in a shaking water bath (80 Hz) for 1 hour. Samples were then filtered through a sterile 250 μm nylon mesh (Scrynel NY250HC, Milian) to remove undigested fragments. The resulting suspension was centrifuged at 1100 RPM for 10 min to separate SVF from adipocytes. Adipocytes were removed and washed with DMEM buffer. They were then suspended in peqGOLD TriFast reagent (Axonlab) and RNA was isolated according to the manufacturer's instructions. The SVF fraction was incubated in erythrocyte lysis buffer (0.154 mM NH4Cl, 10 mM KHCO3, 0.1 mM EDTA) for 2 min. Cells were then centrifuged at 1100 RPM for 10 min and re-suspended in 500 μl of peqGOLD TriFast reagent (Axonlab) for RNA isolation.
Total RNA was isolated from cultured cells using peqGOLD TriFast reagent according to the manufacturer's instructions (Axonlab). First strand cDNA was synthesized from 0.5 μg of total RNA using random primers and Superscript II (Invitrogen). Real time PCR was performed using Power SYBR Green Mix (Applied Biosystem). The following primers were used for mouse genes: SEQ ID NO. 8 (mSipa1I1-F), SEQ ID NO. 9 (mSipa1I1-R), SEQ ID NO. 16 (Ap2-F), SEQ ID NO. 17 (Ap2-R), SEQ ID NO. 12 (mCyclophilin A-F) and SEQ ID NO. 13 (mCyclophilin A-R). The following primers were used for human genes: SEQ ID NO. 10 (hSlap1I1-F), SEQ ID NO. 11 (hSlap1I1-R), SEQ D NO. 14 (hCyclophilin A-F) and SEQ ID NO. 15 (hcyclophilin A-R).
Total RNA from various mouse tissues was isolated using the peqGOLD TriFast reagent according to the manufacturer's instructions (Axonlab). Total RNA (8 μg) was separated on a 1.2% agarose/forlmaldehyde gel and transfected overnight to a nylon membrane. To control for RNA quantity loading, the membrane was stained with methylene blue prior the subsequent hybridizations. For the detection of Sipa1I1 signals, probes from the full-length cDNA mouse plasmid (Open Biosystem) were used. The probes were labeled by random priming with [α-32P]dCTP (Amersham). Hybridization and washing were carried out using the Quickhib method according to manufacturer's instructions (Stratagene). Blots were exposed to Hyperfilm ECL (Amersham) at −80° C. for 1 day or several days depending on the signal intensity.
Bioinformatic analysis of the microarray data was performed to identify genes that fulfilled the three following criteria: (i) regulated by high fat feeding, (ii) similar regulated expression by high fat feeding in both visceral (VAT) and subcutaneous fat (SCAT) and (iii) similar normalization of their expression by rimonabant treatment (
Most importantly, many of the genes cited in table 1 have never been studied in the context of adipose tissue development or biology. These genes belong to the following classes of function: extracellular matrix/cell interaction, cytoskeleton, intracellular signaling, enzymes, and transcription factors/co-factors. They are likely involved in tissue remodeling, and particularly in adipocyte development. One of these genes, Sipa1I1 gene and it role in adipocyte biology, is presented herein and constitutes one aspect of the present invention.
Sipa1I1 belongs to the Rap/Ras GTPase activating protein family and has been described as an anti-apoptotic protein by acting on p53 expression (Tsai I. C. et al., 2007). This protein has also a PDZ domain and can potentially bind to transcription factors and modulate their action on gene transcription.
Acetyl-Coenzyme A dehydrogenase,
medium chain (Acadm)
Amyloid beta (A4) precursor protein (App)
Annexin A2 (Anxa2)
Role in actin-assembly
Calmodulin 1 (Calm1)
Caveolin, caveolae protein 1 Cav1)
Role in lipid homeostasis
Fibroblast growth factor 1 (Fgf1)
Regulator of human adipogenesis
Mesoderm specific transcript (Mest)
Adipocyte differentiation and
enlargement
Nidogen 1 (Nid1)
natriuretic peptide receptor 3 (Npr3)
Possible role in sodium retention
characteristic of obesity associated
hypertension
Phosphatidylinositol 3-kinase, catalytic,
Essential for proper growth factor
alpha polypeptide (Pik3ca)
signaling. Role in adipogenesis.
Secreted acidic cysteine rich glycoprotein
Mediates cell-matrix interactions and
(Sparc)
play a differentiation and angiogenesis.
Spectrin beta 2 (Spnb2)
Zinc finger, DHHC domain containing 2
(Zdhhc2)
Expressed sequence AW112037
RIKEN cDNA B930093H17 gene (like-
glycosyltransferase)
To better understand the role of Sipa1I1 in adipocytes development, its pattern of expression was first characterized. mRNA levels were measured by northern-blot and RT-PCR in various mouse tissues, in isolated preadipocytes and adipocytes, in visceral adipose tissue (VAT) and subcutaneous adipose tissue (SCAT) of mouse obesity model (Ob/Ob mice) and in human adipose tissues.
By northern-blotting, it was shown that Sipa1I1 mRNA was expressed at high level in kidney and showed a weaker expression in all adipose tissues, and at very low level in lung (signals at 5 and 1.5 kb indicated by arrows on
Adipose tissue is a complex tissue that includes not only mature adipocytes, but also precursor cells such as preadipocytes as well as blood vessels, macrophages and fibroblastic cells. Based on a collagenase I digestion technique, stromal vascular fraction (SVF) (including preadipocyte, endothelial and macrophage cells) was separated from the isolated adipocyte fraction. It was found that Sipa1I1 is predominantly expressed in the stromal vascular fraction, containing preadipocytes (
The next step was to determine whether Sipa1I1 gene is conserved among species. To address this question, a RT-PCR was performed on human adipose tissue samples. Preadipocytes and adipocytes were isolated from SCAT or VAT. Isolated preadipocytes were induced to differentiate in vitro until day 7. Results showed that Sipa1I1 is indeed expressed in human fat (
Next, the expression of Sipa1I1 gene was assessed during adipogenesis. For that purpose, mRNA levels were measured by RT-PCR during a detailed differentiation time-course of 3T3-L1 (an adipogenic cell line) (
For the loss-of-function studies, shRNA specific for Sipa1I1 subcloned into a retroviral vector from Clontech were used (RNAi-Ready pSIREN-RetroQ ZsGreen or pSIREN). This plasmid contains a GFP marker, which allows controlling the infection efficiency in 3T3-L1 cells. Two different shRNA for Sipa1I1, were cloned into the pSIREN plasmid, and were first tested in 293T HEK cells. This experiment demonstrated the ability of shRNA specific for Sipa1I1 to inhibit Sipa1I1 expression and obtained 95% and 77% of knockdown with shSipa1I1 (
3T3-L1 cells were then infected for 6 hours with retroviral vectors expressing shRNA directed towards either Sipa1I1 (shSipa1I1) or luciferase (shLuc). Using the GFP marker, we observed 90% infection in the 3T3-L1 cells. At day 0, a 60% knockdown for Sipa1I1 was obtained in cells infected with sSipa1I1 (
| Number | Date | Country | Kind |
|---|---|---|---|
| 09305929.3 | Oct 2009 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB2010/054436 | 10/1/2010 | WO | 00 | 9/27/2012 |
