Patent Application
20090131361
1. Field of the Invention
The present invention relates to novel uses of the MLN 51 gene or protein, in particular, to novel uses of the MLN 51 gene or protein associated with rheumatoid arthritis.
2. Description of the Related Art
Synovial tissue from healthy individuals consists of a single layer of synovial cells without infiltration of inflammatory cells. In synovial tissue of rheumatoid arthritis (RA) patients, lymphocytes and macrophages are recruited and activated, and these activated macrophages release high concentrations of inflammatory cytokines. In response to these cytokines, synovial fibroblasts proliferate vigorously and form villous hyperplastic synovial tissues. These fibroblasts secrete inflammatory mediators, which further attract inflammatory cells and stimulate growth of the synovial fibroblasts as well as that of vascular endothelial cells (1). These activated macrophages and fibroblasts produce tissue-degrading proteinases (2). Thus, the invasive hyperplastic synovial tissue, termed pannus, is directly responsible for structural and functional damage of the affected joints. Therapeutic intervention against RA could be aimed at any one of these steps, but the underlying mechanisms for this are largely unknown. Impaired regulation of apoptosis has been associated with RA (3-5). Recently, however, apoptosis of synovial cells has been identified in rheumatoid synovium (6,7), suggesting that synovial tissue hyperplasia may be a result of cell proliferation rather than that of apoptotic cell death.
Throughout this application, various patents and publications are referenced and citations are provided in parentheses. The disclosure of these patents and publications in their entities are hereby incorporated by references into this application in order to more fully describe this invention and the state of the art to which this invention pertains.
The present inventors have made intensive researches to develop novel biomarkers or therapeutic targets relating to pathogenesis of rheumatoid arthritis (RA), and as a result found that MLN 51 (metastatic lymph node 51) plays a crucial role in RA pathogenesis.
Accordingly, it is an object of this invention to provide a kit for detecting rheumatoid arthritis.
It is another object of this invention to provide a method for screening a substance for preventing or treating rheumatoid arthritis.
It is still another object of this invention to provide a pharmaceutical composition for preventing or treating rheumatoid arthritis.
It is further object of this invention to provide a rheumatoid arthritis-related biomarker.
It is still further object of this invention to provide a method for detecting rheumatoid arthritis.
It is still yet further object of this invention to provide a method for preventing or treating rheumatoid arthritis.
It is another object of this invention to a use of a primer or probe having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1 for manufacturing a composition for detecting rheumatoid arthritis.
It is still another object of this invention to provide a use of an antibody binding specifically to the MLN 51 (metastatic lymph node 51) protein as set forth in SEQ ID NO:2 for manufacturing a composition for detecting rheumatoid arthritis.
It is further object of this invention to provide a use of a substance to inhibit the expression of the MLN 51 (metastatic lymph node 51) gene or the activity of the MLN 51 protein for manufacturing a medicament for detecting preventing or treating rheumatoid arthritis.
Other objects and advantages of the present invention will become apparent from the following detailed description together with the appended claims and drawings.
In one aspect of this invention, there is provided a kit for detecting rheumatoid arthritis, which comprises a primer or probe having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1.
In another aspect of this invention, there is provided a kit for detecting rheumatoid arthritis, which comprises an antibody binding specifically to the MLN 51 protein as set forth in SEQ ID NO:2.
In still another aspect of this invention, there is provided a method for detecting rheumatoid arthritis, which comprises contacting a nucleic acid sample to a probe having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1.
In further aspect of this invention, there is provided a method for detecting rheumatoid arthritis, which comprises amplifying a nucleic acid sample by use of a primer having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1.
In still further aspect of this invention, there is provided a method for detecting rheumatoid arthritis, which comprises contacting a biosample to an antibody binding specifically to the MLN 51 (metastatic lymph node 51) protein as set forth in SEQ ID NO:2.
In still yet further aspect of this invention, there is provided a use of a primer or probe having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1 for manufacturing a composition for detecting rheumatoid arthritis.
In another aspect of this invention, there is provided a use of an antibody binding specifically to the MLN 51 (metastatic lymph node 51) protein as set forth in SEQ ID NO:2 for manufacturing a composition for detecting rheumatoid arthritis.
The present inventors have made intensive researches to develop novel biomarkers relating to pathogenesis of rheumatoid arthritis (RA), and as a result found that MLN 51 (metastatic lymph node 51) plays a crucial role in RA pathogenesis, particularly in chronic synovitis of RA patients.
MLN 51 (metastatic lymph node 51) has been first identified in breast cancer cells (8, 9). Early studies have revealed that MLN 51 plays an essential role in mRNA trafficking from nucleus to cytoplasm (10-12). Recently, its localization, RNA binding module, structural analysis and biological functions were addressed in several reports (8-12).
The present invention is drawn to novel uses of MLN 51, in particular to novel uses of MLN 51 as diagnostic or therapeutic targets for rheumatoid arthritis. The novel use of the present invention is based on our findings that MLN 51 is closely associated with hyperproliferation of RA FLS (rheumatoid arthritis fibroblast-like synoviocyte).
RA is a heterogeneous autoimmune disease. Histologically, RA joints are characterized by chronic inflammation with hyperplasia in the synovial lining cells. It is now well established that FLS (fibroblast-like synoviocyte) actively participate in RA synovitis. FLS in RA joints aggressively proliferate to form a pannus, which eventually destroys articular bone and cartilage. A number of growth factors or cytokines have been described in association with the proliferative response of FLS, such as TGF-β, PDGF, fibroblast growth factor, IL-1β, TNF-α, and IL-6. However, in trials of those therapeutic agents, response was not achieved in a significant proportion of patients, suggesting that some other important factors still remain undiscovered. To our best knowledge, the present invention is a first report or suggestion that MLN 51 plays a critical role in hyperproliferation of RA FLS.
The probes or primers used in the present kit has a complementary sequence to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1. The term “complementary” with reference to sequence used herein refers to a sequence having complementarity to the extent that the sequence anneals or hybridizes specifically with the nucleotide sequence of the MLN 51 gene set forth in SEQ ID NO:1 under certain annealing or hybridization conditions. In this regard, the term “complementary” used herein has different meaning from the term “perfectly complementary”. The probes or primers used in the present invention can be one or more mismatch, so long as such mismatches are not sufficient to completely preclude specific annealing or hybridization to the MLN 51 gene.
As used herein the term “probe” means a linear oligomer of natural or modified monomers or linkages, including deoxyribonucleotides and ribonucleotides, capable of specifically binding to a target polynucleotide. The probe may be naturally occurring or artificially synthesized. The probe is preferably single stranded. Preferably, the probes used in the present invention are oligodeoxyribonucleotides. The probe of this invention can be comprised of naturally occurring dNMP (i.e., dAMP, dGM, dCMP and dTMP), modified nucleotide, or non-natural nucleotide. The primer can also include ribonucleotides. For instance, the probes of this invention may include nucleotides with backbone modifications such as peptide nucleic acid (PNA) (M. Egholm et al., Nature, 365:566-568 (1993)), phosphorothioate DNA, phosphorodithioate DNA, phosphoramidate DNA, amide-linked DNA, MMI-linked DNA, 2′-O-methyl RNA, alpha-DNA and methylphosphonate DNA, nucleotides with sugar modifications such as 2′-O-methyl RNA, 2′-fluoro RNA, 2′-amino RNA, 2′-O-alkyl DNA, 2′-O-allyl DNA, 2′-O-alkynyl DNA, hexose DNA, pyranosyl RNA, and anhydrohexitol DNA, and nucleotides having base modifications such as C-5 substituted pyrimidines (substituents including fluoro-, bromo-, chloro-, iodo-, methyl-, ethyl-, vinyl-, formyl-, ethynyl-, propynyl-, alkynyl-, thiazolyl-, imidazolyl-, pyridyl-), 7-deazapurines with C-7 substituents (substituents including fluoro-, bromo-, chloro-, iodo-, methyl-, ethyl-, vinyl-, formyl-, alkynyl-, alkenyl-, thiazolyl-, imidazolyl-, pyridyl-), inosine, and diaminopurine.
The term “primer” as used herein refers to an oligonucleotide, which is capable of acting as a point of initiation of synthesis when placed under conditions in which synthesis of primer extension product which is complementary to a nucleic acid strand (template) is induced, i.e., in the presence of nucleotides and an agent for polymerization, such as DNA polymerase, and at a suitable temperature and pH. The suitable length of primers will depend on many factors, including temperature, application and source of primer, generally, 15-30 nucleotides in length. Shorter primers generally need lower temperature to form stable hybridization duplexes to templates.
The sequences of primers are not required to have perfectly complementary sequence to templates. The sequences of primers may comprise some mismatches, so long as they can be hybridized with templates and serve as primers. Therefore, the primers of this invention are not required to have perfectly complementary sequence to the MLN 51 gene as templates; it is sufficient that they have complementarity to the extent that they anneals specifically to the nucleotide sequence of the MLN 51 gene for acting as a point of initiation of synthesis. The primer design may be conveniently performed with referring to the MLN 51 gDNA or cDNA sequences, preferably, cDNA sequence. For instance, the primer design may be carried out using computer programs for primer design (e.g., PRIMER 3 program). Exemplified primers of this invention is set forth in SEQ ID NO:3 (sense primer) and SEQ ID NO:4 (antisense primer).
According to a preferred embodiment, the diagnosis or detection kit for rheumatoid arthritis comprising probes is in the form of microarray, more preferably DNA or cDNA microarray, most preferably cDNA microarray.
In microarray, the present probes serve as hybridizable array elements and are immobilized on substrates. A preferable substrate includes suitable solid or semi-solid supporters, such as membrane, filter, chip, slide, wafer, fiber, magnetic or nonmagnetic bead, gel, tubing, plate, macromolecule, microparticle and capillary tube. The hybridizable array elements are arranged and immobilized on the substrate. Such immobilization occurs through chemical binding or covalent binding such as UV. In an embodiment of this invention, the hybridizable array elements are bound to a glass surface modified to contain epoxy compound or aldehyde group or to a polylysin-coated surface. Further, the hybridizable array elements are bound to a substrate through linkers (e.g. ethylene glycol oligomer and diamine).
DNAs to be examined with a microarray of this invention may be labeled, and hybridized with array elements on microarray. Various hybridization conditions are applicable, and for the detection and analysis of the extent of hybridization, various methods are available depending on labels used.
The present method for diagnosing rheumatoid arthritis may be carried out in accordance with hybridization. For such analysis, probes, which have a complementary sequence to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1, are used.
Using probes hybridizable with the MLN 51 gene or cDNA, preferably cDNA, rheumatoid arthritis is diagnosed or detected by hybridization-based assay. According to a preferred embodiment, some modifications in the probes of this invention can be made unless the modifications abolish the advantages of the probes. Such modifications, i.e., labels linking to the probes generate a signal to detect hybridization. Suitable labels include fluorophores (e.g., fluorescein), phycoerythrin, rhodamine, lissamine, Cy3 and Cy5 (Pharmacia), chromophores, chemiluminescers, magnetic particles, radioisotopes (e.g., P32 and S35), mass labels, electron dense particles, enzymes (e.g., alkaline phosphatase and horseradish peroxidase), cofactors, substrates for enzymes, heavy metals (e.g., gold), and haptens having specific binding partners, e.g., an antibody, streptavidin, biotin, digoxigenin and chelating group, but not limited to. Labeling is performed according to various methods known in the art, such as nick translation, random priming (Multiprime DNA labeling systems booklet, “Amersham” (1989)) and kination (Maxam & Gilbert, Methods in Enzymology, 65:499 (1986)). The labels generate signal detectable by fluorescence, radioactivity, measurement of color development, mass measurement, X-ray diffraction or absorption, magnetic force, enzymatic activity, mass analysis, binding affinity, high frequency hybridization or nanocrystal.
The nucleic acid sample (preferably, cDNA) to be analyzed may be prepared using mRNA from various biosamples. The biosample is preferably a cell from synovial tissues, most preferably FLS (fibroblast-like synoviocyte). Instead of probes, cDNA may be labeled for hybridization-based analysis.
Probes are hybridized with cDNA molecules under stringent conditions for detecting rheumatoid arthritis. Suitable hybridization conditions may be routinely determined by optimization procedures. Conditions such as temperature, concentration of components, hybridization and washing times, buffer components, and their pH and ionic strength may be varied depending on various factors, including the length and GC content of probes and target nucleotide sequence. The detailed conditions for hybridization can be found in Joseph Sambrook, et al., Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001); and M. L. M. Anderson, Nucleic Acid Hybridization, Springer-Verlag New York Inc. N.Y. (1999). For example, the high stringent condition includes hybridization in 0.5 M NaHPO4, 70% SDS (sodium dodecyl sulfate) and 1 mM EDTA at 65° C. and washing in 0.1×SSC (standard saline citrate)/0.1% SDS at 68° C. Also, the high stringent condition includes washing in 6×SSC/0.05% sodium pyrophosphate at 48° C. The low stringent condition includes e.g., washing in 0.2×SSC/0.1% SDS at 42° C.
Following hybridization reactions, a hybridization signal indicative of the occurrence of hybridization is then measured. The hybridization signal may be analyzed by a variety of methods depending on labels. For example, where probes are labeled with enzymes, the occurrence of hybridization may be detected by reacting substrates for enzymes with hybridization resultants. The enzyme/substrate pair useful in this invention includes, but not limited to, a pair of peroxidase (e.g., horseradish peroxidase) and chloronaphthol, aminoethylcarbazol, diaminobenzidine, D-luciferin, lucigenin (bis-A methylacridinium nitrate), resorufin benzyl ether, luminol, Amplex Red reagent (10-acetyl-3,7-dihydroxyphenoxazine), HYR (p-phenylenediamine-HCl and pyrocatechol), TMB (3,3,5,5-tetramethylbenzidine), ABTS (2,2-Azine-di[3-ethylbenzthiazoline sulfonate]), o-phenylenediamine (OPD) or naphthol/pyronine; a pair of alkaline phosphatase and bromochloroindolylphosphate (BCIP), nitro blue tetrazolium (NBT), naphthol-AS-B1-phosphate or ECF substrate; and a pair of glucosidase and t-NBT (nitroblue tetrazolium) or m-PMS (phenazine methosulfate). Where probes are labeled with gold particles, the occurrence of hybridization may be detected by silver staining method using silver nitrate.
In these connections, where the present method for diagnosing rheumatoid arthritis is carried out by hybridization, it comprises the steps of (i) contacting a nucleic acid sample to a probe having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 (metastatic lymph node 51) gene as set forth in SEQ ID NO:1; and (ii) detecting the occurrence of hybridization.
The signal intensity from hybridization is indicative of rheumatoid arthritis. When the hybridization signal to MLN 51 cDNA from a sample to be diagnosed is measured to be stronger than normal samples (or osteoarthritis samples), the sample can be determined to have rheumatoid arthritis.
According to a preferred embodiment, the primers of this invention are used for amplification reactions.
The term used herein “amplification reactions” refers to reactions for amplifying nucleic acid molecules. A multitude of amplification reactions have been suggested in the art, including polymerase chain reaction (hereinafter referred to as PCR) (U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159), reverse transcription-polymerase chain reaction (hereinafter referred to as RT-PCR) (Sambrook, J. et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)), the methods of Miller, H. I. (WO 89/06700) and Davey, C. et al. (EP 329,822), ligase chain reaction (LCR) (17, 18), Gap-LCR (WO 90/01069), repair chain reaction (EP 439,182), transcription-mediated amplification (TMA) (19) (WO 88/10315), self sustained sequence replication (WO 90/06995), selective amplification of target polynucleotide sequences (U.S. Pat. No. 6,410,276), consensus sequence primed polymerase chain reaction (CP-PCR) (U.S. Pat. No. 4,437,975), arbitrarily primed polymerase chain reaction (AP-PCR) (U.S. Pat. Nos. 5,413,909 and 5,861,245), nucleic acid sequence based amplification (NASBA) (U.S. Pat. Nos. 5,130,238, 5,409,818, 5,554,517, and 6,063,603), strand displacement amplification and loop-mediated isothermal amplification (LAMP), but not limited to. Other amplification methods that may be used are described in, U.S. Pat. Nos. 5,242,794, 5,494,810, 4,988,617 and in U.S. Ser. No. 09/854,317.
According to the most preferred embodiment, the amplification reaction is carried out in accordance with PCR (polymerase chain reaction) which is disclosed in U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159.
PCR is one of the most predominant processes for nucleic acid amplification and a number of its variations and applications have been developed. For example, for improving PCR specificity or sensitivity, touchdown PCR (24), hot start PCR (25, 26), nested PCR (2) and booster PCR (27) have been developed with modifying traditional PCR procedures. In addition, real-time PCR, differential display PCR (DD-PCR), rapid amplification of cDNA ends (RACE), multiplex PCR, inverse polymerase chain reaction (IPCR), vectorette PCR, thermal asymmetric interlaced PCR (TAIL-PCR) and multiplex PCR have been suggested for certain applications. The details of PCR can be found in McPherson, M. J., and Moller, S. G. PCR. BIOS Scientific Publishers, Springer-Verlag New York Berlin Heidelberg, N.Y. (2000), the teachings of which are incorporated herein by reference in its entity.
Where the present method for diagnosing rheumatoid arthritis is carried out using primers, the nucleic acid amplification is executed for analyzing the expression level of the MLN 51 gene. Because the present invention is intended to assess the expression level of the MLN 51 gene, the level of the MLN 51 mRNA in samples (e.g., FLS) is analyzed.
Therefore, the present invention performs nucleic acid amplifications using mRNA molecules in samples as templates and primers to be annealed to mRNA or cDNA.
For obtaining mRNA molecules, total RNA is isolated from samples. The isolation of total RNA may be performed by various methods (Sambrook, J. et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001); Tesniere, C. et al., Plant Mol. Biol. Rep., 9:242 (1991); Ausubel, F. M. et al., Current Protocols in Molecular Biology, John Willey & Sons (1987); and Chomczynski, P. et al., Anal. Biochem. 162:156 (1987)). For example, total RNA in cells may be isolated using Trizol. Afterwards, cDNA molecules are synthesized using mRNA molecules isolated and then amplified. Since total RNA molecules used in the present invention are isolated from human samples, mRNA molecules have poly-A tails and converted to cDNA by use of dT primer and reverse transcriptase (PNAS USA, 85:8998 (1988); Libert F, et al., Science, 244:569 (1989); and Sambrook, J. et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)). cDNA molecules synthesized are then amplified by amplification reactions.
The primers used for the present invention is hybridized or annealed to a region on template so that double-stranded structure is formed. Conditions of nucleic acid hybridization suitable for forming such double stranded structures are described by Joseph Sambrook, et al., Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001) and Haymes, B. D., et al., Nucleic Acid Hybridization, A Practical Approach, IRL Press, Washington, D.C. (1985).
A variety of DNA polymerases can be used in the amplification step of the present methods, which includes “Klenow” fragment of E. coli DNA polymerase I, a thermostable DNA polymerase and bacteriophage T7 DNA polymerase. Preferably, the polymerase is a thermostable DNA polymerase such as may be obtained from a variety of bacterial species, including Thermus aquaticus (Taq), Thermus thermophilus (Tth), Thermus filiformis, Thermis flavus, Thermococcus literalis, and Pyrococcus furiosus (Pfu).
When a polymerization reaction is being conducted, it is preferable to provide the components required for such reaction in excess in the reaction vessel. Excess in reference to components of the amplification reaction refers to an amount of each component such that the ability to achieve the desired amplification is not substantially limited by the concentration of that component. It is desirable to provide to the reaction mixture an amount of required cofactors such as Mg2+, and dATP, dCTP, dGTP and dTTP in sufficient quantity to support the degree of amplification desired. All of the enzymes used in this amplification reaction may be active under the same reaction conditions. Indeed, buffers exist in which all enzymes are near their optimal reaction conditions. Therefore, the amplification process of the present invention can be done in a single reaction volume without any change of conditions such as addition of reactants.
Annealing or hybridization in the present method is performed under stringent conditions that allow for specific binding between the primer and the template nucleic acid. Such stringent conditions for annealing will be sequence-dependent and varied depending on environmental parameters.
The amplified MLN 51 cDNA molecules are then analyzed to assess the expression level of the MLN 51 gene. For example, the amplified products are resolved by a gel electrophoresis and the bands generated are analyzed to assess the expression level of the MLN 51 gene. When the expression level of the MLN 51 gene from a sample to be diagnosed is measured to be higher than normal samples (or osteoarthritis samples), the sample can be determined to have rheumatoid arthritis.
In these connections, where the present method for diagnosing rheumatoid arthritis is carried out by amplification, it comprises the steps of (i) amplifying a nucleic acid sample by use of a primer having a nucleotide sequence complementary to the nucleotide sequence of the MLN 51 gene as set forth in SEQ ID NO:1; and (ii) analyzing the amplified products to determine the expression level of the MLN 51 gene.
The diagnosing kit for rheumatoid arthritis may be constructed by incorporating an antibody binding specifically to the MLN 51 protein as set forth in SEQ ID NO:2.
The antibody against the MLN 51 protein used in this invention may polyclonal or monoclonal, preferably monoclonal. The antibody could be prepared according to conventional techniques such as a fusion method (Kohler and Milstein, European Journal of Immunology, 6:511-519 (1976)), a recombinant DNA method (U.S. Pat. No. 4,816,56) or a phage antibody library (Clackson et al, Nature, 352:624-628 (1991) and Marks et al, J. Mol. Biol., 222:58, 1-597 (1991)). The general procedures for antibody production are described in Harlow, E. and Lane, D., Antibodies: A Laboratory Manual, Cold Spring Harbor Press, New York, 1988; Zola, H., Monoclonal Antibodies: A Manual of Techniques, CRC Press, Inc., Boca Raton, Fla., 1984; and Coligan, CURRENT PROTOCOLS IN IMMUNOLOGY, Wiley/Greene, NY, 1991, which are incorporated herein by references. For example, the preparation of hybridoma cell lines for monoclonal antibody production is done by fusion of an immortal cell line and the antibody producing lymphocytes. This can be done by techniques well known in the art. Polyclonal antibodies may be prepared by injection of the MLN 51 protein antigen to suitable animal, collecting antiserum containing antibodies from the animal, and isolating specific antibodies by any of the known affinity techniques.
Where the diagnosing method of this invention is performed using antibodies to the MLN 51 protein, it could be carried out according to conventional immunoassay procedures for detecting rheumatoid arthritis.
Such immunoassay may be executed by quantitative or qualitative immunoassay protocols, including radioimmunoassay, radioimmuno-precipitation, enzyme-linked immunosorbent assay (ELISA), capture-ELISA, inhibition or competition assay, sandwich assay, flow cytometry, immunofluorescence assay and immuoaffinity assay, but not limited to. The immunoassay and immunostaining procedures can be found in Enzyme Immunoassay, E. T. Maggio, ed., CRC Press, Boca Raton, Fla., 1980; Gaastra, W., Enzyme-linked immunosorbent assay (ELISA), in Methods in Molecular Biology, Vol. 1, Walker, J. M. ed., Humana Press, NJ, 1984; and Ed Harlow and David Lane, Using Antibodies: A Laboratory Manual, Cold Spring Harbor Press, 1999, which are incorporated herein by references.
For example, according to the radioimmunoassay method, the radioisotope (e.g., C14, I125, P32 and S35) labeled antibody may be used to detect the MLN 51 protein.
In addition, according to the ELISA method, the example of the present method may comprise the steps of: (i) coating a surface of solid substrates with cell (e.g., FLS) lysate to be analyzed; (ii) incubating the coated cell lysate with a primary antibody to the MLN 51 protein; (iii) incubating the resultant with a secondary antibody conjugated with an enzyme; and (iv) measuring the activity of the enzyme.
The solid substrate useful in this invention includes carbohydrate polymer (e.g., polystyrene and polypropylene), glass, metal and gel, most preferably microtiter plates.
The enzyme conjugated with the secondary antibody is that catalyzing colorimetric, fluorometric, luminescence or infra-red reactions, e.g., including alkaline phosphatase, β-galactosidase, luciferase, Cytochrome P450 and horseradish peroxidase. Where using alkaline phosphatase, bromochloroindolylphosphate (BCIP), nitro blue tetrazolium (NBT) or ECF may be used as a substrate for color-developing reactions; in the case of using horseradish peroxidase, chloronaphthol, aminoethylcarbazol, diaminobenzidine, D-luciferin, lucigenin (bis-N-methylacridinium nitrate), resorufin benzyl ether, luminol, Amplex Red reagent (10-acetyl-3,7-dihydroxyphenoxazine), HYR (p-phenylenediamine-HCl and pyrocatechol), TMB (3,3,5,5-tetramethylbenzidine), ABTS (2,2-Azine-di[3-ethylbenzthiazoline sulfonate]), o-phenylenediamine (OPD) or naphthol/pyronine may be used as a substrate; and in the case of using glucose oxidase, t-NBT (nitroblue tetrazolium) or m-PMS (phenazine methosulfate) may be used as a substrate.
Where the present method is performed in accordance with the capture-ELISA method, the specific example of the present method may comprise the steps of: (i) coating a surface of a solid substrate with a capturing antibody capable of binding specifically to the MLN 51 protein; (ii) incubating the capturing antibody with a cell sample (e.g., FLS) to be analyzed; (iii) incubating the resultant of step (ii) with a detecting antibody which is capable of binding specifically to the MLN 51 protein and conjugated with a label generating a detectable signal; and (iv) detecting the signal generated from the label conjugated with the detecting antibody.
The detecting antibody has a label generating a detectable signal. The label includes, but not limited to, a chemical (e.g., biotin), an enzymatic (e.g., alkaline phosphatase, horseradish peroxidase, β-galactosidase and Cytochrome P450), a radioactive (e.g., C14, I125, P32 and S35), a fluorescent (e.g., fluorescein), a luminescent, a chemiluminescent and a FRET (fluorescence resonance energy transfer) label. Various labels and methods for labeling antibodies are well known in the art (Ed Harlow and David Lane, Using Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory Press, 1999).
The detection of the signal generated from the label conjugated with the detecting antibody can be carried out by various processes well known in the art. The detection of the signal enables to analyze the MLN 51 protein in a quantitative or qualitative manner. Where biotin and luciferase are used as labels, the signal detection may be achieved by use of streptavidin and luciferin, respectively.
The measurement of signal intensities generated from the immunoassay described above is indicative of rheumatoid arthritis. When the signal to the MLN 51 protein in a biosample to be diagnosed is measured to be higher than normal samples, the biosample can be determined to have rheumatoid arthritis.
The kit of the present invention may optionally include other reagents along with primers, probes or antibodies described above. For instance, where the present kit may be used for nucleic acid amplification, it may optionally include the reagents required for performing PCR reactions such as buffers, DNA polymerase (thermostable DNA polymerase obtained from Thermus aquaticus (Taq), Thermus thermophilus (Tth), Thermus filiformis, Thermis flavus, Thermococcus literalis, and Pyrococcus furiosus (Pfu)), DNA polymerase cofactors, and deoxyribonucleotide-5-triphosphates. The kits, typically, are adapted to contain in separate packaging or compartments the constituents afore-described.
The kits for detecting or diagnosing rheumatoid arthritis permit to determine the development, aggravation and alleviation of rheumatoid arthritis. In this regard, the term used herein “detecting or diagnosing” with reference to disease means not only the determination of the existence of disease but also the development, aggravation and alleviation of disease.
According to a preferred embodiment, the kits and methods of the present invention is used to detect or diagnose rheumatoid arthritis developed by hyperproliferation of FLS (fibroblast-like synoviocyte).
The present method for detecting rheumatoid arthritis can diagnose conditions of rheumatoid arthritis in much more effective and accurate manner, and determine rheumatoid arthritis differentially from osteoarthritis.
In another aspect of this invention, there is provided a method for screening a substance for preventing or treating rheumatoid arthritis, which comprises the steps of: (a) contacting the substance to be analyzed to a cell containing the MLN 51 (metastatic lymph node 51) gene or protein; and (b) measuring the expression level of the MLN 51 gene, the amount of the MLN 51 protein or the activity of the MLN 51 protein, wherein if the expression level of the MLN 51 gene, the amount of the MLN 51 protein or the activity of the MLN 51 protein is measured to be down-regulated, the substance has a potency to prevent or treat rheumatoid arthritis.
According to the present method, cells containing the MLN 51 gene or protein are first contacted to substances to be analyzed. Preferably, cells containing the MLN 51 gene or protein are rheumatoid arthritis fibroblast-like synoviocyte. The term “substance” used herein in conjunction with the present screening method refers to a material tested in the present method for analyzing the influence on the expression level of the MLN 51 gene, the amount of the MLN 51 protein or the activity of the MLN 51 protein. The substance includes chemical substances, nucleotides, antisense-RNA, siRNA (small interference RNA) and extract of natural source, but not limited to.
Afterwards, the expression level of the MLN 51 gene, the amount of the MLN 51 protein or the activity of the MLN 51 protein in cells is measured. Where the expression level of the MLN 51 gene, the amount of the MLN 51 protein or the activity of the MLN 51 protein is measured to be down-regulated, the substance is determined to be a candidate to prevent or treat rheumatoid arthritis.
The measurement of the expression level of the MLN 51 gene could be carried out by a variety of methods known in the art. For example, RT-PCR (Sambrook et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)), Northern blotting (Peter B. Kaufma et al., Molecular and Cellular Methods in Biology and Medicine, 102-108, CRC press), hybridization using cDNA microarray (Sambrook et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)) and in situ hybridization (Sambrook et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)) may be used.
Where the expression level of the MLN 51 gene is analyzed by RT-PCT, total RNA is first isolated from cells treated with a substance to be analyzed and a first cDNA strand is then synthesized using oligo dT primer and reverse transcriptase. Then, PCR amplifications are performed using the first cDNA strand as templates and a MLN 51-specific primer set which is exemplified in SEQ ID NOs:3 and 4. Finally, the PCR amplified products are resolved by electrophoresis and bands are analyzed for assessing the expression level of the MLN 51 gene.
The amount of the MLN 51 protein is determined by various immunoassays known in the art. For example, radioimmunoassay, radioimmuno-precipitation, enzyme-linked immunosorbent assay (ELISA), capture-ELISA, inhibition or competition assay and sandwich assay are used for analyzing the amount of the MLN 51 protein.
In still another aspect of this invention, there is provided a pharmaceutical composition for preventing or treating rheumatoid arthritis, which comprises a substance to inhibit the expression of the MLN 51 gene or the activity of the MLN 51 protein as an active ingredient.
In further aspect of this invention, there is provided a method for preventing or treating rheumatoid arthritis, which administering to a subject a substance to inhibit the expression of the MLN 51 (metastatic lymph node 51) gene or the activity of the MLN 51 protein.
In still further aspect of this invention, there is provided a use of a substance to inhibit the expression of the MLN 51 (metastatic lymph node 51) gene or the activity of the MLN 51 protein for manufacturing a medicament for detecting preventing or treating rheumatoid arthritis.
The pharmaceutical composition of this invention may comprise chemical substances, nucleotides, antisense oligonucleotides, siRNA oligonucleotides or extract of natural source.
According to a preferred embodiment, the substance to inhibit the expression of the MLN 51 gene is an antisense or siRNA oligonucleotide having a complementary sequence to the nucleotide sequence of SEQ ID NO:1.
The term used herein “antisense oligonucleotide” used herein is intended to refer to nucleic acids, preferably, DNA, RNA or its derivatives, that are complementary to the base sequences of a target mRNA, characterized in that they binds to the target mRNA and interfere its translation to protein. The antisense oligonucleotide of this invention means DNA or RNA sequences complementary and binding to MLN 51 mRNA of SEQ ID NO:1, that are able to inhibit translation, translocation, maturation or other biological functions of MLN 51 mRNA. The antisense nucleic acid is 6-100, preferably, 8-60, more preferably, 10-40 nucleotides in length.
The antisense oligonucleotide may comprise at least one modification in its base, sugar or backbone for its higher inhibition efficacy (De Mesmaeker et al., Curr Opin Struct Biol, 5(3):343-55 (1995)). The modified nucleic acid backbone comprises phosphorothioate, phosphotriester, methyl phosphonate, short chain alkyl or cycloalkyl intersugar linkages or short chain heteroatomic or heterocyclic intersugar linkages. The antisense oligonucleotide may also contain one or more substituted sugar moieties. The antisense nucleic acid may include one or more modified bases, for example, hypoxanthine, 6-methyladenine, 5-me pyrimidines (particularly, 5-methylcytosine), 5-hydroxymethylcytosine (HMC), glycosyl HMC and gentobiosyl HMC, as well as synthetic nucleobases, e.g., 2-aminoadenine, 2-(methylamino)adenine, 2-(imidazolylalkyl)adenine, 2-(aminoalkylamino)adenine or other heterosubstituted alkyladenines, 2-thiouracil, 2-thiothymine, 5-bromouracil, 5-hydroxymethyluracil, 8-azaguanine, 7-deazaguanine, N6(6-aminohexyl)adenine and 2,6-diaminopurine. Another modification of the oligonucleotides of the invention involves chemically linking to the oligonucleotide one or more moieties or conjugates which enhance the activity or cellular uptake of the oligonucleotide. Such moieties include but are not limited to lipid moieties such as a cholesterol moiety, a cholesteryl moiety (Letsinger et al., Proc. Natl. Acad. Sci. USA, 86:6553 (1989)), cholic acid (Manoharan et al. Bioorg. Med. Chem. Let, 4:1053 (1994)), a thioether, e.g., hexyl-5-tritylthiol (Manoharan et al. Ann. N.Y. Acad. Sci., 660:306 (1992); Manoharan et al. Bioorg. Med. Chem. Let, 3: 2765 (1993)), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 20:533 (1992)), an aliphatic chain, e.g., dodecandiol or undecyl residues (Saison-Behmoaras et al. EMBO J., 10:111 (1991); Kabanov et al. FEBS Lett., 259:327 (1990); Svinarchuk et al. Biochimie, 75:49 (1993), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethylammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate (Manoharan et al. Tetrahedron Lett., 36:3651 (1995); Shea et al. Nucl. Acids Res., 18:3777 (1990)), a polyamine or a polyethylene glycol chain (Manoharan et al. Nucleosides & Nucleotides, 14:969 (1995)), or adamantane acetic acid (Manoharan et al. Tetrahedron Lett., 36: 3651 (1995)). Oligonucleotides comprising lipophilic moieties, and methods for preparing such oligonucleotides are known in the art, for example, U.S. Pat. Nos. 5,138,045, 5,218,105 and 5,459,255. The modifications described above enhance stability against nuclease degradation and increase affinity of the antisense oligonucleotide toward its target mRNA.
The antisense molecule is conventionally synthesized in vitro and then transmitted to cells. In addition, it is intracellularly produced by transcription from foreign sequence. In vitro synthesis involves RNA polymerase I. In vivo transcription for preparing antisense RNA uses vector having origin of recognition region (MCS) in opposite orientation. The antisense RNA preferably comprises a translation stop codon for inhibiting translation to peptide.
According to a preferred embodiment, the antisense oligonucleotide of this invention has a complementary sequence to the nucleotide sequence spanning nucleotides 200-700 of SEQ ID NO:1.
The pharmaceutical composition of this invention comprises as an active ingredient a siRNA oligonucleotide having a complementary sequence to the nucleotide sequence of SEQ ID NO:1.
The term “siRNA” used herein refers to a nucleic acid molecule mediating RNA interference or gene silencing (see WO 00/44895, WO 01/36646, WO 99/32619, WO 01/29058, WO 99/07409 and WO 00/44914). The siRNA to inhibit expression of a target gene provides effective gene knock-down method or gene therapy method. It was been first in plants, insects, Drosophila melanogaster and parasites and recently has been used for mammalian cell researches.
The siRNA molecule of this invention may consist of a sense RNA strand (having sequence corresponding to MLN 51 mRNA) and an antisense RNA strand (having sequence complementary to MLN 51 mRNA) and form a duplex structure. Alternatively, the siRNA molecule of this invention may have a single strand structure comprising self-complementary sense and antisense strands.
The siRNA of this invention is not restricted to a RNA duplex of which two strands are completely paired and may comprise non-paired portion such as mismatched portion with non-complementary bases and bulge with no opposite bases. The overall length of the siRNA is 10-100 nucleotides, preferably, 15-80 nucleotides, and more preferably, 20-70 nucleotides.
The siRNA may comprise either blunt or cohesive end so long as it enables to silent the MLN 51 expression due to RNAi effect. The cohesive end may be prepared in 3′-end overhanging structure or 5′-end overhanging structure.
The siRNA may be constructed by inserting a short nucleotide sequence (e.g., about 5-15 nt) between self-complementary sense and antisense strands. The siRNA expressed forms a hairpin structure by intramolecular hybridization, resulting in the formation of stem-and-loop structure. The stem-and-loop structure is processed in vitro or in vivo to generate active siRNA molecule mediating RNAi.
According to a preferred embodiment, the siRNA oligonucleotide of this invention has a complementary sequence to the nucleotide sequence spanning nucleotides 200-700 of SEQ ID NO:1. Most preferably, the siRNA oligonucleotide of this invention is a double stranded oligonucleotide having SEQ ID NOs:5 and 6.
The pharmaceutically acceptable carrier contained in the pharmaceutical composition of the present invention, which is commonly used in pharmaceutical formulations, but is not limited to, includes lactose, dextrose, sucrose, sorbitol, mannitol, starch, rubber arable, potassium phosphate, arginate, gelatin, potassium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrups, methylcellulose, methyl hydroxy benzoate, propylhydroxy benzoate, talc, magnesium stearate, and mineral oils. The pharmaceutical composition according to the present invention may further include a lubricant, a humectant, a sweetener, a flavoring agent, an emulsifier, a suspending agent, and a preservative. Details of suitable pharmaceutically acceptable carriers and formulations can be found in Remington's Pharmaceutical Sciences (19th ed., 1995), which is incorporated herein by reference.
A pharmaceutical composition of this invention may be administered orally or parenterally (e.g., intravenous injection, subcutaneous injection, intramuscular injection and local injection).
The correct dosage of the pharmaceutical compositions of this invention will be varied according to the particular formulation, the mode of application, age, body weight and sex of the patient, diet, time of administration, condition of the patient, drug combinations, reaction sensitivities and severity of the disease. According to a preferred embodiment of this invention, a daily suitable dosage unit for human host ranges from 0.001-100 mg/kg (body weight).
According to the conventional techniques known to those skilled in the art, the pharmaceutical compositions of this invention can be formulated with pharmaceutical acceptable carrier and/or vehicle as described above, finally providing several forms including a unit dosage form. Non-limiting examples of the formulations include, but not limited to, a solution, a suspension or an emulsion, an extract, an elixir, a powder, a granule, a tablet, a capsule, emplastra, a liniment, a lotion and an ointment.
In another aspect of this invention, there is provided a rheumatoid arthritis-related biomarker, comprising the MLN 51 (metastatic lymph node 51) gene of SEQ ID NO:1 or the MLN 51 protein of SEQ ID NO:2.
The biomarker of this invention is significantly specific to rheumatoid arthritis, in particular chronic synovitis.
The present invention will now be described in further detail by examples. It would be obvious to those skilled in the art that these examples are intended to be more concretely illustrative and the scope of the present invention as set forth in the appended claims is not limited to or by the examples.
FLS cells (RA s-2, 2-6, 2-14, 2-18, 2-36 and 2-38) were prepared from synovectomized tissue of RA patients undergoing joint replacement surgery. Informed consent was obtained from each patient enrolled. The mean age of the patients was 43.8 years, and the disease duration was more than 24 months for all patients. All had erosions visible on radiographs of the hand. All of the RA patients satisfied the diagnostic criteria of American College of Rheumatology (formerly, the American Rheumatism Association) for the classification of RA [13]. RA FLSs were prepared as described previously [14-16]. Briefly, to set up cell lines, synovial tissues were minced into 2-3-mm pieces and treated for 4 hr with 4 mg/ml type 1 collagenase (Worthington Biochemicals, Freehold, N.J., USA) in Dulbecco's modified Eagle's medium (DMEM) at 37° C. in 50% CO2. Dissociated cells were centrifuged at 500 g and were resuspended in DMEM supplemented with 10% FCS, 2 mM L-glutamine, 100 U/ml penicillin, and 100 μg/ml streptomycin. Suspended cells were plated in 75-cm2 culture flasks and cultured at 37° C. in 5% CO2. Medium was replaced every 3 days, and once the primary culture reached confluence, cells were split weekly. Cells at passages 5 to 8 contained a homogeneous population of FLS (<2.5% CD14+, <1% CD3+, and <1% CD19+ in flow cytometry analysis) [14]. Osteoarthritis (OA) FLSs used as the control were prepared from the synovial tissues of three OA patients enrolled. Synovial fluid samples were obtained from the knee joints of different six patients with active RA.
Immature bone marrow-derived dendritic cells (BmDCs) were generated from bone marrow (BM) precursor cells of DBA/1J mice (Japan SLC, Inc.) as described previously [17]. Briefly, bone marrow cells were harvested from femurs and tibias of mice and plated in RPMI-1640 medium supplemented with 10% FBS, 50 μM 2-mercaptoethanol, and high dose (200 U/ml) murine granulocyte macrophage-colony stimulating factor (GM-CSF; Endogen, Inc., Cambridge, Calif.). The medium was changed every other day. Seven days later, non-adherent cells (immature DCs) were harvested by gentle washing with warm PBS. For DC maturation, cells were stimulated for 24 hr with TNF-α (500 U/ml; Endogen, Inc., Cambridge, Calif.) or with LPS (1 μg/ml; Sigma-Aldrich; E. coli, 0127:B8) together with anti-CD40 (clone 3/23 or HM40, 5 μg/ml; BD Pharmingen). The purity and maturation status of DCs were analyzed by a flow cytometer (FACS Calibur; BD Biosciences, San Jose, Calif.) using FITC-conjugated CD44, CD80, CD86, CD205 and MHC II monoclonal antibodies (mAb) or PE-conjugated CD11c, CD40 and ICOSL mAb (BD PharMingen, San Diego, Calif.). Data were analyzed using Cell Quest Software.
The BC-1 cells (DC cell line; kindly provided by Dr. Onoe, Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan), generated from BALB/c mouse spleen [18,19], were cultured and expanded in R1 medium, IMDM containing 10% FCS, 30% NIH/3T3 culture supernatant, and 10 ng/mL mouse recombinant GM-CSF. The BC-1 cells exhibit an immature dendritic cell phenotype.
cDNA Microarray Analysis of RA FLS
We used two kinds of immunologic cDNA microarray chips, HI380 and MI380 (Creagene Inc., Seoul, Korea) for this study. Total RNA was extracted using TRIZOL reagent (InVitrogen, Carlsbad, Calif.) and purified by using RNeasy total RNA isolation kit (Qiagen, Valencia, Calif.) according to the manufacturer's instructions. Gene expression profile of human RA-FLS and mouse BmDC were analyzed by using HI380 and MI380 microarray chips, consisting of 384 human and mouse cDNA clones, respectively. Twenty μg of total RNA was reverse-transcribed in the presence of Cy-3 or Cy-5 conjugated dUTP (Amersham Pharmacia Biotech, Piscataway, N.J.) respectively, using SuperScript II and oligo-(dT) 18 primer (InVitrogen, Carlsbad, Calif.) in a reaction volume of 20 μl according to the method suggested by the manufacturer. After the labeling reaction for 1 hr at 42° C., unincorporated florescent nucleotides were cleaned up using Microcon YM-30 column (Millipore, Bedford, Mass.). The Cy-3 and Cy-5 labeled cDNA probes were mixed together and hybridized to a microarray slide. After overnight at 65° C., the slide was washed twice with 2×SSC containing 0.1% SDS for 5 min at 42° C., once with 0.1×SSC containing 0.1% SDS for 10 min at room temperature, and finally with 0.1×SSC for 1 min at room temperature. Slide was dried by centrifugation at 650 rpm for 5 min. Hybridization images on the slide were scanned by Scanarray lite (Packard Bioscience, Boston, Mass.) and analyzed by GenePix Pro3.0 software (Axon Instrument, Union city, Calif.). Three independent experiments were performed and the ratio of Cy-3 and Cy-5 signal intensity was calculated for each spot. These ratios were log 2-transformed and normalized by subtracting the average of log 2 (Cy3/Cy5) values for internal control genes using Excel (Office 2003, Microsoft Corp.) [21]. For each gene, the mean values were then calculated and a difference of two fold was applied to select up- or down-regulated genes in RA/OA FLSs or immature DC/BM progenitors.
In order to confirm the up- or down-regulation of the selected gene (MLN51) on the microarray analysis and the expression of MLN51 after siRNA transfection, total RNAs were extracted from RA FLSs using TRIZOL reagent (InVitrogen, Carlsbad, Calif.) and purified using RNeasy total RNA isolation kit (Qiagen, Valencia, Calif.) according to the manufacturer's instructions. One μg of total RNA was mixed with 50 μM oligo(dT)20, and 10 mM dNTP mix, heated at 65° C. for 5 min, and place on ice for at least 1 min. Then 10×RT buffer [25 mM MgCl2, 0.1 M DTT, RNaseOUT™ (40 U/l)] and SuperScript™ III RT (200 U/l) were added, and the mixture was incubated at 42° C. for 1 hr. The reaction was terminated at 75° C. for 5 min and then chilled on ice. The PCR was performed using the cDNA as template and certain gene specific-primers. Primers used in this study were: hMLN51 forward, 5′-AAGACACCGAGGACGAGGAATC-3′ hMLN51 reverse, 5′-CCTTCCATAGCTTTCGCTGACG-3′ product size 600 bp; mMLN51 forward, 5′-TCCCTGCCCTGCCCTGACTTTA-3′, mMLN51 reverse, 5′-CCTCGCGTGCTGTGGGAACTCT-3′ product size 800 bp and GAPDH forward, 5′-CCACAGTCCATGCCATCAC-3′, GAPDH reverse, 5′-TCCACCACCCTGTTGCTGTA-3′ product size 500 bp. The initial cDNA content in each sample was normalized with the amount of glyceraldehyde-3-phosphate dehydrogenase (GAPDH). Amplification reactions were performed in a 20 μl volume using 5 ng or 10 ng of each cDNA on a Perkin-Elmer DNA thermocycler 9600 Prism for 35 cycles. The PCR reactions were separated on 1.2% agarose gels and stained with ethidium bromide.
IL-1β and TNF-α were measured in the SFs using the Human Cytometric Bead Array (CBA) (BD Pharmingen, San Diego, Calif.), and GM-CSF using the Human ELISA kits (Endogen, Inc., Cambridge, Mass.) following the manufacturer's instructions.
RA FLS samples were lysed in boiled buffer containing 1% SDS. Each sample, containing a normalized amount of total protein (about 30 μg of protein), was separated by 10% SDS-PAGE and transferred to a nitrocellulose membrane. This was then immersed in blocking buffer (5% skimmed milk and 0.1% Tween 20 in PBS, pH 7.4) for 1 hr at room temperature and incubated with anti-hMLN51 rabbit serum (1:1,000 dilution) and anti-GAPDH (1:5,000 dilution) or anti-α-tubulin (1:5,000 dilution) in blocking buffer overnight at 4° C. Anti-hMLN51 serum was obtained from rabbits immunized with recombinant hMLN51 protein. After the incubation, the membrane was probed with horseradish peroxidase-labeled anti-rabbit IgG antibody (1:5,000 dilution) in PBS (containing of 0.05% Tween 20 and 5% skimmed milk powder) for 30 minutes at room temperature. The proteins in the membrane were detected by enhanced chemiluminescence (Amersham, Little Chalfont, Bucks., UK) and bands were detected by autoradiography with X-ray film (Fujifilm).
Treatment of RA FLS with SF, Cytokine or Neutralizing Antibodies
RA FLSs were cultured in a 12-well plates in high glucose DMEM supplemented with 10% FBS, penicillin, streptomycin, and glutamine at 37° C. in a 5% CO2 humidified incubator. In case of SF and cytokines-treatment, RA FLSs were treated with SFs to recover their growth as follows: 1/100, 1/50, or 1/10 dilution in culture media. Human Inflammatory cytokines (IL-1β, and TNF-α, 100 ng/ml of each) and growth factor (GM-CSF, 10 or 100 ng/ml) were obtained from Pepro Tech, Rocky Hill, N.J. or BD Pharmingen, San Diego, Calif. Monoclonal neutralizing antibodies to GM-CSF (BVD2-23B6, IgG2a, 300 ng/ml), IL-1β (AS10, IgG1, 500 ng/ml) and TNF-α (MAb1, IgG1, 2 μg/ml) were purchased from BD Pharmingen, San Diego, Calif. During the experiments, the trypan blue exclusion method was employed for the evaluation for cell proliferation.
siRNA Synthesis and Transfection
The siRNA synthesis was performed using the Silencer™ siRNA Cocktail Kit (RNase III; Ambion Inc., Austin, Tex.). The siRNA sequence was used for targeted silencing of human MLN51 [Genebank access number: NM007359] and mouse MLN51 [Genebank access number: AJ292072]. The oligonucleotides used for the dsRNA synthesis were in hMLN51, 5′-TAATACGACTCACTATAGGGTACTCGTAAGATGGCGGACCGG and 5′-TAATACGACTCACTATAGGGTCCGTCCCCACTTTGCCTC, and in mMLN51, 5′-TAATACGACTCACTATAGGGTACTCGTAAGATGGCGGACCGG-3′ and 5′-TAATACGACTCA CTATAGGGTACTCTGCCTCTCCCCAGTCAC-3′. The siRNA sequences were selected in size ranging from 228 to 686 bp, as described previously [20,21]. The siRNA synthesis was performed according to the manufacturer's protocol. Non-silencing or negative control siRNA (Silencer™ Negative Control #2 siRNA; Ambion Inc.) is an irrelevant siRNA with random nucleotides and no known specificity. Ten thousand RA FLS per well were seeded in 24-well plates in DMEM supplemented with 10% FBS. The cells were transfected with the siRNA on the next day using GenePORTER 2 Transfection Reagent™ (Gene Therapy Systems, San Diego, Calif.) according to the manufacturer's protocol. After 24 hr post-transfection, the media was added with the fresh DMEM supplemented with 10% FBS. Everyday the cells were harvested, and then counted. Total RNA extracted from the transfected cells was used to perform semi-quantitative RT-PCR.
The results are expressed as the mean±SEM. The Mann-Whitney Utest was used for all statistical analysis. A p value of less than 0.05 was considered significant.
RA is a heterogeneous autoimmune disease. However, these heterogeneous chronic diseases are recently able to be monitored in line with their gene expression patterns by microarray in molecular studies [24]. Histologically, RA joints are characterized by chronic inflammation with hyperplasia in the synovial lining cells. It is now well established that FLS actively participate in RA synovitis. FLS in RA joints aggressively proliferate to form a pannus, which eventually destroys articular bone and cartilage [25,26]. A number of growth factors or cytokines have been described in association with the proliferative response of FLS, such as TGF-β, PDGF, fibroblast growth factor, IL-1β, TNF-α, and IL-6. However, in trials of those therapeutic agents, response was not achieved in a significant proportion of patients, suggesting that some other important factors still remain undiscovered.
To our knowledge the present invention is the first demonstration of the ability of MLN51 gene to be essential for tumorigenicity of RA FLS in vitro under investigation by siRNA gene knock-down experiments. Our results show that the SF-mediated growth of RA FLS was markedly blocked by anti-GM-CSF neutralizing antibody, and additionally growth-retarded RA-FLS recovered their proliferation capacity by adding GM-CSF into the culture. These results imply that GM-CSF in SF plays an important role for the hyperproliferation of RA FLS. Moreover, in the microarray analysis and semi-quantitative RT-PCR, we found that the MLN51 gene was highly expressed in the hyperactive RA FLS in low passage or RA FLS cultured in the presence of SF. MLN51 knock-down by siRNA completely blocked the GM-CSF/SF-mediated hyperproliferation of RA FLS, suggesting that the MLN51 is strongly involved in the chronic synovitis in RA patients.
Firstly, we extracted total RNA from RA FLSs and one OA FLS as a control, which were labeled and hybridized to HI380 microarrays containing 384 gene clones. The differential hybridization was performed with Cy-5-labeled RA cDNA and Cy-3-labeled OA cDNA probes. Through the microarray analysis, we found that MLN51, a novel gene in association with RA, was markedly upregulated among the many upregulated genes selected on the basis of their immunologic characteristics (Table 1).
We next performed semi-quantitative RT-PCR with the MLN51 gene selected in the analysis to confirm the differences observed in cDNA microarray analysis. MLN51 overexpression in RA FLSs was confirmed by RT-PCR analysis with three different RA FLS samples (
We next investigated whether SFs have an effect on recovery of the reduced growth of high passage No. RA FLS or not, which one of factors in SFs have a growth-recovering effect and whether the recovering factor plays a role in the expression of MLN51 or not. First of all, we observed the morphology of RA FLS (RA 2-14) on the different passage with the inverted microscope. As shown in
It has been reported that there are many kinds of cytokines and growth factors in RA microenvironments. To identify factors having an effect on the growth of RA FLS, we investigated the effects of the inflammatory cytokines or growth factor on the growth of RA FLS (2-14) in vitro. The results show that GM-CSF and TNF-α may have an effect on recovering the growth of high passage No. RA FLS (
Moreover, to investigate the effects of IL-1β or TNF-α in SF on recovering the growth of RA FLS, we cultured the RA FLS in SF-containing media in the presence of anti-GM-CSF, anti-GM-CSF+anti-IL-1β or anti-GM-CSF+anti-TNF-α mAbs. As shown in
On the other hand, to examine the specific requirement for hMLN51 gene in cell proliferation, siRNA prepared from the 5′ region of human MLN51 cDNA was introduced into passage No. 5 RA FLS. The growth kinetics of the transfected RA FLS was monitored for 5 days, and the level of the corresponding hMLN51 mRNA was measured by semi-quantitative RT-PCR. We observed that the treatment of FLS with hMLN51-siRNA causes a complete abrogation of RA FLS proliferation (
We next generated the BmDCs from DBA/13 mice frequently used as an arthritis model. It is known that DBA/1 mouse strain having H-2q haplotype readily develop arthritis after immunization with heterologous or autologous type II collagen, including rat, bovine or chick CII [29]. Also, DCs are particularly relevant in a pathogenesis of most inflammatory arthropathies because of their potent Ag-presenting activity and unique ability to activate naïve T cells [30-32]. In addition, DC populations have been described in the synovial membrane in RA, although their functional contribution to disease remains difficult to assess [33-35]. The immature BmDCs were generated from BM progenitors by culturing progenitors in the presence of GM-CSF alone. Immature BmDCs were matured with LPS and anti-CD40. And we then performed semi-quantitative RT-PCR of MLN51 gene expression to confirm the differences observed in cDNA microarray analysis. As shown in
Taken together, our results strongly suggest that the MLN51 whose expression is depending on the GM-CSF signaling, may have a critical role in the hyperproliferation of FLS in RA pathogenesis.
The present invention provides a kit for detecting rheumatoid arthritis, a method for screening a substance for preventing or treating rheumatoid arthritis, a pharmaceutical composition for preventing or treating rheumatoid arthritis and a rheumatoid arthritis-related biomarker. The MLN 51 gene and protein is closely related to the development of rheumatoid arthritis and serve as biomarker and therapeutic target for rheumatoid arthritis, particularly chronic synovitis.
Having described a preferred embodiment of the present invention, it is to be understood that variants and modifications thereof falling within the spirit of the invention may become apparent to those skilled in this art, and the scope of this invention is to be determined by appended claims and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2006-0041646 | May 2006 | KR | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/KR07/02259 | 5/8/2007 | WO | 00 | 11/7/2008 |
