Patent Application
20110177526
Incorporated by reference herein in its entirety is the Sequence Listing filed in the parent application, U.S. patent application Ser. No. 12/354,668, filed Jan. 15, 2009 with the U.S. Patent and Trademark Office, size of 27 kilobytes.
The present invention relates generally to the field of transmembrane signal transduction. More specifically, the invention relates to the components of multisubunit receptors for cytokines, and assays for detecting interactions between these components.
Protein tyrosine kinases (PTK) are critical enzymes for receptor-mediated signal transduction in lymphocytes. Indeed, protein tyrosine phosphorylation is an early and requisite event in signaling for both multichain immune recognition receptors such as the T-cell antigen receptor (TCR) and cytokine receptors. Unlike growth factor receptors, neither the TCR nor the cytokine receptors have intrinsic PTK activity. Rather, they are coupled to nonreceptor tyrosine kinases. For example, the src family PTK, Lck and Fyn have been implicated in TCR-mediated signaling. The non-src family PTK Zap-70 has been shown to associate with the TCR upon activation. The src family PTK, Lck, Fyn and Lyn have also been implicated in Interleukin-2 (IL-2) receptor mediated signaling.
The Janus family kinases (JAKs) represent a recently described family of PTK. These kinases, called JAK-1, JAK-2 and Tyk-2, are structurally quite distinct in that they possess tandem nonidentical catalytic domains. These PTK are ubiquitously expressed and have been shown to participate in signaling by a number of cytokine and hormone receptors. These PTK are believed to exert their effects through tyrosyl phosphorylated transcription factors.
IL-2 is a T-cell lymphokine that both functions as a potent autocrine growth factor and activates other cells, including B-cells and natural killer (NK) cells. In addition, the interaction of IL-2 with high affinity IL-2 receptors regulates the magnitude and duration of the normal T-cell immune response.
High affinity IL-2 receptors comprise three receptor components, denoted the IL-2 receptor α, β and the common γ (γc) chain. Interestingly, the γc chain is a receptor component that is shared by the receptors for several of the interleukins. In the mechanism of IL-2 signal transduction, IL-2 binding induces heterodimerization of the cytoplasmic domains of β and γc. This heterodimerization is required for IL-2 signaling.
While the IL-2 receptor is a multi-subunit complex that lacks intrinsic enzymatic activity, it is clear that protein tyrosine phosphorylation is an early biochemical step that follows ligand binding. Occupancy of the IL-2 receptor additionally stimulates alkalinization of T-cells via Na+/H+ exchange, activation of Ras, Raf and ERK1, induction of the fos, jun and myc proto-oncogenes, as well as induction of effector functions such as cytotoxicity and cellular proliferation.
One aspect of the invention provides an isolated polynucleotide encoding the JAK-3 protein. The JAK-3 protein is a protein tyrosine kinase that has a molecular weight of approximately 125 kDa. In addition, the JAK-3 protein is characterized by tandem non-identical catalytic domains. The JAK-3 protein lacks SH2 or SH3 domains, and is expressed in NK cells and stimulated or transformed T-cells, but not substantially expressed in resting T-cells. In a preferred embodiment, the isolated polynucleotide encoding the JAK-3 protein has the nucleotide sequence of SEQ ID NO:8.
A second aspect of the invention relates to an isolated JAK-3 protein. The JAK-3 protein is a protein tyrosine kinase having a molecular weight of approximately 125 kDa, has tandem non-identical catalytic domains, lacks SH2 or SH3 domains, and is expressed in NK cells and stimulated or transformed T-cells, but not substantially expressed in resting T-cells. In a preferred embodiment, the isolated JAK-3 protein has the polypeptide sequence of SEQ ID NO:9.
A third aspect of the invention relates to an antibody that is specific to JAK-3 protein. As described above, the JAK-3 protein is a protein tyrosine kinase having a molecular weight of approximately 125 kDa. The JAK-3 protein recognized by the claimed antibody has tandem non-identical catalytic domains, lacks SH2 or SH3 domains, and is expressed in NK cells and stimulated or transformed T-cells, but not substantially expressed in resting T-cells. In a preferred embodiment, the antibody that specifically recognizes the JAK-3 protein is polyclonal.
A fourth aspect of the invention provides a method of identifying an agent having immunomodulating activity. This method includes first determining the ability of the β or γc chain of the IL-2 receptor to physically associate with a Janus family kinase selected from the group consisting of JAK-1 and JAK-3 in the absence of a candidate immunomodulatory agent. A second step includes determining the ability of a chain of the IL-2 receptor to physically associate with a Janus family kinase in the presence of the candidate immunomodulating agent. If the candidate immnomodulating agent causes either a lesser or greater ability of the IL-2 receptor chain and the Janus family kinase to associate with each other, then such an ability will indicate that the candidate agent has immunomodulating activity. In a preferred embodiment, the two determining steps are performed in the presence of a cytokine compound. In a more preferred embodiment, the cytokine compound is a cytokine compound that binds to a receptor that includes the γc chain. In yet a more preferred embodiment, the cytokine compound is selected from the group consisting of IL-2, IL-4, IL-7, IL-9 and IL-15. In another preferred embodiment, each of the determining steps includes immunoprecipitating a chain of the IL-2 receptor with an antibody that is specific to that chain, and then determining if the Janus family kinase coprecipitates with that receptor chain. According to this embodiment, the candidate agent can be a peptide fragment of the γc chain of the IL-2 receptor.
A fifth aspect of the invention relates to a method of identifying a therapeutic agent for modulating the immune system. This method includes first isolating a Janus family kinase selected from the group consisting of JAK-1 and JAK-3. A subsequent step involves determining the ability of the kinase to phosphorylate a substrate in the absence of a candidate agent, and then determining the ability of the kinase to phosphorylate the substrate in the presence of the candidate agent. A decrease in the ability of the kinase to phosphorylate the substrate in the presence of the candidate agent indicates that said candidate agent is an immunosuppressive agent. Alternatively, a greater ability of the kinase to phosphorylate the substrate in the presence of the candidate agent indicates that said candidate agent is an immuno-enhancing agent. In a preferred embodiment, the isolating step includes immunoprecipitating the Janus family kinase with an antibody specific to the Janus family kinase. In a more preferred embodiment, each of the determining steps includes first reacting the Janus family kinase with γ-labeled ATP to produce reaction products, and then separating the reaction products by electrophoresis and identifying the labeled products. In an even more preferred embodiment, each of the determining steps includes first reacting the Janus family kinase with ATP to produce reaction products, then separating the reaction products by electrophoresis, exposing the separated reaction products to a labeled antibody specific for phosphotyrosine, and finally identifying the reaction products that exhibit binding to the antibody.
We have discovered that a novel protein tyrosine kinase (PTK), called JAK-3, has structural features characteristic of the Janus family of PTK. Unlike the three other members of this family, JAK-3 is only expressed in a narrow spectrum of cell types. Whereas JAK-1, JAK-2 and Tyk2 are broadly expressed, JAK-3 is the first Janus family member that exhibits limited tissue expression, or that is induced following cellular activation. In particular, JAK-3 was found to be predominantly expressed in activated human T lymphocytes and NK cells. We also have observed JAK-3 expression in IFN-γ activated human peripheral blood monocytes and B-cells. Based on this pattern of gene expression, we believe that the function of JAK-3 is related to important signaling pathways in these cell types. However, we acknowledge that JAK-3 could also be inducible in nonhematopoietic tissues by appropriate stimuli.
Herein we disclose that IL-2 can rapidly induce activation and tyrosine phosphorylation of JAK-3 in responsive cells. Additionally, we show that JAK-1, although less prominently tyrosine-phosphorylated, also is involved in IL-2 receptor signaling. The data presented below indicate that both JAK-3 and JAK-1 play important roles in lymphoid activation via the IL-2 receptor. Specifically, JAK-3 and JAK-1 associate with other components of the IL-2 receptor to form an activated receptor complex. Thus, agents that inhibit the interaction of either JAK-1 or JAK-3 with other components of the receptor are considered as candidates for immunomodulatory drugs. We contemplate that such immunomodulatory drugs can be either immunosuppressing or immunoenhancing.
More specifically, compounds that inhibit the interaction of JAK-1 with IL-2Rβ, or the interaction of JAK-3 with the γc subunit of the IL-2 receptor complex are expected to inhibit IL-2 dependent signal transduction. These inhibitory compounds can act through mechanisms involving drug interaction with the kinase, or with the receptor substrate. In the first instance, the compound may interact with the kinase such that the kinase fails to phosphorylate the receptor chain. Alternatively, the inhibitor may act on the kinase such that it fails to autophosphorylate. According to another contemplated mechanism, the inhibitory compound may interact with one of the chains of a multisubunit receptor, so that interaction with the Janus family kinase is inhibited. Finally, we contemplate compounds which disrupt the binding between one receptor chain and the Janus family kinase that ordinarily binds to that receptor subunit.
The development of assays for identifying compounds that inhibit IL-2 dependent signalling represents an important step toward the discovery of novel immunomodulators. Compounds having inhibitor activity in such assays will be identified as potential therapeutics for the treatment of autoimmune diseases and transplant rejection. Autoimmune diseases anticipated as objects of therapy using drugs identified according to the assays disclosed herein include, but are not limited to, rheumatoid arthritis, psoriatic arthritis, lupus and vasculitis. Certain of the drugs identified according to the present invention are likely to be useful not only in the treatment of disorders resulting from inappropriate activation of the IL-2 receptor, but also from inappropriate activation of other cytokine receptors that share common subunits with the IL-2 receptor.
Our approach to the development of an assay for compounds that inhibit IL-2 dependent signalling stems from our understanding of the detailed structure of the IL-2 receptor complex. In particular, we have discovered that two different Janus family tyrosine kinases interact with different subunits of the IL-2 receptor. Binding of the JAKs to the receptor subunits represents a critical step in the cytokine signalling pathway. It follows that any agent that disrupts or prevents this binding will also inhibit IL-2 dependent signalling. Thus, we have designed an assay to identify compounds that inhibit interactions between components of the IL-2 receptor complex as a method for identifying candidate agents for modulating the immune system.
Direct physical interactions of IL-2Rβ with JAK-1 and γc with JAK-3 were demonstrated during the development of the present invention. IL-2 increased JAK-3 association with the IL-2 receptor, with an apparent increase of γc-JAK-3 association and de novo induction of IL-2Rβ-JAK-3 interaction. Truncation of γc resulted in its failure to associate with JAK-3. Moreover, a patient having a mild form of X-linked combined immunodefficiency (XCID) that was characterized by diminished IL-2 induced proliferation had a γc point mutation (Leu 271 changed to Gln) that decreased γc association with JAK-3. Thus, γc mutations, in at least some XSCID and XCID patients, can inhibit the ability of γc to associate with JAK-3. The severity of this immunodeficiency owes to the fact that γc is a component of multiple cytokine receptors.
Indeed, the sharing of the γc subunit of the IL-2 receptor by other cytokine receptors, including receptors for IL-4, IL-7, IL-9 and IL-15, has led us to believe that any compound which inhibits the cytokine induced binding of JAK-3 to the γc chain would also inhibit signalling through the receptors for any of these cytokines. Thus, we believe that an assay for compounds that inhibit cytokine induced binding of JAK-3 to the γc chain is useful in the discovery of drugs that could be used to treat autoimmune diseases that are attributable to the activities of IL-2, IL-4, IL-7, IL-9 and IL-15.
Although other materials and methods similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are now described. General references for methods that can be used to perform the various PCR and cloning procedures and nucleic acid and protein blotting procedures described herein can be found in Molecular Cloning: A Laboratory Manual (Sambrook et al. eds. Cold Spring Harbor Lab Publ. 1989) and Current Protocols in Molecular Biology (Ausubel et al. eds., Greene Publishing Associates and Wiley-Interscience 1987). The disclosures contained in these publications are hereby incorporated by reference. A description of the experiments and results that led to the creation of the present invention follows.
We employed the PCR approach described by Harpur et al., in Oncogene 7:1347 (1992) and by Siliciano et al., in Proc. Natl. Acad. Sci. USA 89:11194 (1992) to amplify novel PTK encoding sequences expressed in NK cells. The disclosures of these Harpur et al. and Siliciano et al. references are incorporated by reference. Briefly, we first prepared cDNA from NK cell mRNA using reverse transcriptase. We then performed PCR using degenerate oligonucleotide primers corresponding to conserved motifs in the catalytic domains of PTK. The forward primers were designed to correspond to residues in subdomain VI and to exclude src-family PTK. The reverse primer corresponded to the reverse complement of the DVWSFG (SEQ ID NO:1) motif (subdomain IX) conserved in a large number of PTK.
Example 1 describes the methods used to isolate an amplified polynucleotide that corresponded to the JAK-3 tyrosine kinase.
First strand cDNA was prepared from total RNA that had been isolated from NK cell RNA according to standard methods. The cDNA prepared in this fashion served as the template in a subsequent PCR reaction.
The forward primer used in this PCR reaction was 5′-CCA GCG GCC GCG T(G/A/T/C)CA (C/T)CG (G/A/T/C)GA (C/T)C T(G/A/T/C)GC-3′ (SEQ ID NO:2) and the reverse primer was 5′-CCA GCG GCC GCC C(G/A)A A(G/A/T/C/) (G/C) (A/T)CC A(G/A/T/C)A C(G/A)T C-3′ (SEQ ID NO:3). The resulting products were digested with NotI, subcloned and sequenced. The PCR fragment corresponding to one novel kinase was isolated, labeled and used to screen several cDNA libraries. Among the libraries screened were oligo (dT) primed cDNA libraries derived from PHA stimulated peripheral blood T-cells and the HUT-78 T-cell line (Clonetech, Palo Alto, Calif.) in the λgtll cloning vector, a λ ZAP YT library and a λ ZAP library from PHA activated T-cells. Purified phage DNA was digested and subcloned into pBLUESCRIPT (Stratagene, La Jolla, Calif.) for nucleic acid sequencing. Sequence data were manipulated and analyzed using the programs of the Genetics Computer Group of the University of Wisconsin and the BLAST program of NCBI.
For Northern analysis, total RNA from various human tissues was either purchased from Clonetech (Palo Alto, Calif.) or prepared from NK cells and T-cells. Northern blotting was carried out according to standard procedures. Blots were probed with radiolabeled nucleic acid probes corresponding to the PCR amplified fragment described above.
Results indicated that one of the candidate clones isolated by this method was preferentially expressed in NK and activated T-cells as an approximately 4.3 kb mRNA.
Thus, the DNA fragment amplified using kinase-specific primers exhibited a tissue-specific pattern of mRNA expression. We therefore proceeded to isolate a cDNA clone that contained the entire reading frame for the protein that was partly encoded by the amplified fragment. We have termed this protein “JAK-3.”
Example 2 describes the method used to determine the DNA sequence of the polynucleotide that encoded the putative tissue-restricted kinase obtained in Example 1.
The PCR generated fragment from Example 1 was used as a probe to screen phage cDNA libraries prepared from the NK-like cell line, YT, PHA-activated T-cells and HUT-78 cells. Approximately 5×105 plaques from each library were screened to obtain multiple overlapping clones that generated a polynucleotide sequence corresponding to a single long open reading frame. SEQ ID NO:9 provides the predicted amino acid sequence encoded by the NK cell derived JAK-3 cDNA. We note that a published report by Kawamura et al. (Proc. Natl. Acad. Sci. USA 91:6374 (1994)) refers to the JAK-3 protein disclosed herein as “L-JAK.” The polynucleotide sequence encoding the JAK-3 protein has been filed in GenBank under accession number U09607 and is provided herein as SEQ ID NO:8.
The open-reading frame of this polynucleotide sequence encompasses 3372 nucleotides and is predicted to encode a polypeptide having 1124 residues. The molecular weight of the predicted polypeptide is 125,014 Da. This value is roughly equivalent to, but slightly smaller than, other JAKs. As described below, this predicted molecular weight is consistent with the Mr of the polypeptide identified by Western blotting using the antiserum prepared against JAK-3.
The predicted protein encoded by the JAK-3 polynucleotide exhibited structural features characteristic of a PTK, as would readily be appreciated by one having ordinary skill in the art. Like other PTK, a catalytic domain is present in the C-terminal portion of the molecule (subdomains I-XI). This domain begins with a typical ATP-binding motif at residues 829-834 (subdomain 1) in which the canonical GXGXXG (SEQ ID NO:4) motif is evident and is followed by a critical lysine residue in subdomain II (residue 855). Just C-terminal to subdomain VII is a pair of tyrosine residues following an acidic residue that could represent the autophosphorylation site. In subdomain VIII, phenylalanine and tyrosine residues surround the invariant tryptophan residue. We note that the locations of the subdomains cited herein are identified by Kawamura et al. in Proc. Natl. Acad. Sci. USA 91:6374 (1994), the disclosure of which is hereby incorporated by reference. This atypical motif contrasts with the motifs seen in src and abl related proteins, and growth factor receptors. Notably though, this motif (FWYAPE) (SEQ ID NO:5) is present in the Janus family kinases. The Janus family of PTK comprises PTK that have tandem nonidentical catalytic domains and a large extracatalytic segment. These structural features of the Janus family of PTK have been considered by Wilks et al., in Mol. Cell. Biol. 11:2057 (1991), Harpur et al., in Oncogene 7:1347 (1992), and Firmbach-Kraft et al., in Oncogene 5:1329 (1990). The entire catalytic domain, termed the JAK homology (JH) 1 domain, comprises 273 amino acids (residues 822 to 1095) and is followed by a unique C-terminus.
In addition to a kinase catalytic domain, the predicted JAK-3 protein has a region N-terminal to the PTK catalytic domain that also has elements typical of a protein kinase catalytic domain. This tandem kinase-like (JH-2) domain is a characteristic feature of the JAKs, and has been described by Harpur et al., in Oncogene 7:1347 (1992), Firmbach-Kraft et al., in Oncogene 5:1329 (1990), Velazquez et al., in Cell 70:313 (1992), and Argetsinger et al., Cell 74:237 (1993). Like other Janus family kinases, this domain in the NK derived JAK-3 protein lacks some standard features of a PTK catalytic domain. In particular, the JAK-3 protein appears to lack an autophosphorylation site in subdomain VII.
The known JAK family PTK have large extracatalytic segments (JH 3-7 domains) located N-terminal to the kinase (JH1) and kinase-like (JH2) domains. While motifs corresponding to SH2 or SH3 domains are lacking, there is a motif that Harpur et al., (Oncogene 7:1347 (1992)) suggested to have SH2-like character. This region is conserved in three of the four family members, including the JAK-3 protein. Immediately N-terminal to this motif is a highly conserved motif that is a possible tyrosine phosphorylation site (VDGYFRL) (SEQ ID NO:6). Other areas of striking homology between the novel JAK-3 protein and other JAKs are also evident in the remaining domains (JH 5-7).
The findings presented above indicated the NK-derived isolate had nearly all of the characteristics of a JAK family PTK. Protein homology analysis indicated the overall identity of the NK PTK to the most closely related Janus family member, JAK-2, was approximately 68%. The fact that a hydrophilicity plot showed no evidence for a hydrophobic domain suggested that the JAK-3 polynucleotide sequence encoded a non-receptor type PTK.
Other members of the Janus family of PTK (JAK-1, JAK-2, and Tyk2) have been shown to be present in a variety of tissues. These findings have been described by Wilks et al., in Mol. Cell. Biol. 11:2057 (1991), Harpur et al., in Oncogene 7:1347 (1992), and Firmbach-Kraft et al., in Oncogene 5:1329 (1990). Given this precedent, we proceeded to determine if JAK-3 was also broadly expressed across different tissues and cell types. As described below, we unexpectedly discovered that JAK-3 expression is tissue-restricted.
Example 3 describes the methods used to determine the expression profile for the JAK-3 mRNA.
Total RNA (20 μg) from various human tissues (purchased from Clonetech), NK cells and T-cells was electrophoresed in formaldehyde/agarose gels, transferred to membranes and probed with a radiolabeled cDNA corresponding to the JH1 and JH2 domains of JAK-3. T-cells were activated with PHA for 24 hours prior to RNA isolation. NK cells were activated with IL-2 (1,000 units/ml) for 24 hours prior to RNA isolation. Uniform RNA loading in the different lanes of the Northern blot was confirmed by ethidium bromide staining and by hybridization with a probe that detected ribosomal RNA.
Unexpectedly, and in contrast to other Janus family members, JAK-3 exhibited a restricted pattern of mRNA expression across different tissues. In the absence of stimulation, the mRNA was only detected in NK cells. Notably, activation of NK cells did not alter the level of JAK-3 mRNA expression. The JAK-3 mRNA was also detected at high levels in activated NK cells and activated T-cells. No JAK-3 mRNA was detected in liver, testis, kidney, small intestine, brain or lung tissues. Hybridization of the same Northern Filter with a JAK-1 cDNA probe gave evidence for mRNA expression in all tissues except for small intestine. Interestingly, while the JAK-3 mRNA was expressed at very low levels in resting T-cells, the mRNA was induced upon T-cell activation.
Various cultured cell lines were also tested for expression of the JAK-3 mRNA. As expected, our results indicated the JAK-3 mRNA was constitutively expressed in the NK-like YT cell line. As predicted by studies with peripheral blood T-cells, the JAK-3 mRNA was not constitutively expressed in the Jurkat T-cell line but was induced upon activation. Interestingly, we found that JAK-3 mRNA was constitutively expressed in the HUT-78 transformed T-cell line. No expression of this gene was detected in a variety of other cell lines, including the erythroleukemia cell line, K562.
We next identified a unique portion of the C-terminal region of the JAK-3 protein and generated a corresponding synthetic peptide for use as an immunogen. The conclusion regarding protein sequence uniqueness was based on the results from a computer-assisted comparison between the JAK-3 amino acid sequence and all sequences available through the Program Manual for the Wisconson Package, Version 8, September 1994, Genetics Computer Group, (575 Science Dr. Madison, Wis. 53711). This search protocol included searches of the GenBank, GenPept, SwissProt, Brookhaven and EMBL databases. The synthetic peptide used in our procedures corresponded to amino acids 1104-1124 of the JAK-3 protein.
Example 4 describes the immunological methods used to analyze the JAK-3 protein.
A peptide corresponding to the predicted C-terminus of the JAK-3 protein (amino acids 1104-1124) was synthesized (Multiple Peptide Systems, San Diego, Calif.), coupled to keyhole limpet hemocyanin (KLH) with MBS (Pierce, Rockford, Ill.) and used to immunize rabbits. HUT-78 cells (107 cells per point) were labeled with 35S methionine (0.5 mCi/ml) for 2 hours, washed with phosphate buffered saline and lysed in buffer containing 1% TRITON™ X-100 detergent (lysis buffer). Postnuclear supernatants were immunoprecipitated with 10 μl of antiserum prebound to protein A sepharose washed in buffer containing 0.1% TRITON™ X-100 detergent (wash buffer), eluted and electrophoresed in 8% polyacrylamide gels that were subsequently fixed, rinsed in FLUORO-HANCE™ fluorographic enhancer (Research Products Inc., Mount Prospect, Ill.) and dried for autoradiography.
For immunoblot analysis, cells were solubilized in lysis buffer and postnuclear supernatants (approximately 100 μg of protein) were electrophoresed, transferred to nitrocellulose and immunoblotted. Filters were blocked, incubated with antiserum (1:1000), washed and incubated with peroxidase conjugated goat antirabbit IgG, all according to standard methods well known in the art. Antibody binding was detected by enhanced chemiluminescence (ECL) (Amersham Corp.).
In good agreement with the molecular weight predicted by the deduced JAK-3 primary structure, analysis of metabolically labeled HUT-78 cells showed specific immunoprecipitation of a polypeptide with a Mr of approximately 125 kDa. Immunoblot analysis of these cells also showed reactivity of the antibody with a protein of approximately the same mobility in HUT-78. In contrast Jurkat T-cells expressed minimal levels of this protein. In additional experiments, the expression of the JAK-3 encoded polypeptide was found to parallel the expression seen by analysis of mRNA. Expression of the protein was detected in NK cells, activated T-cells and in some transformed leukocyte cell lines. Immunoblotting with preimmune serum or antiserum competed with cognate peptide versus irrelevant peptide, thus confirming the specificity of this reactivity.
The results obtained in Example 4 confirmed that antibodies raised against a JAK-3 specific synthetic peptide could be used to immunoprecipitate the JAK-3 protein from cellular lysates. However, these results provided no insight into the function of the JAK-3 protein. Thus, to ascertain whether the JAK-3 protein had enzymatic activity, in vitro kinase assays were performed.
Example 5 describes the in vitro assay used to demonstrate that immunoprecipitated JAK-3 protein had kinase activity.
Kinase assays were performed as described by Muller et al., in Nature 366:129 (1993), and by Watling et al., in Nature 366:166 (1993). According to these procedures, cells were solubilized in lysis buffer supplemented with 1 mM Na3VO4 and 1 mM EDTA. An antipeptide antiserum was then used to carry out an immunoprecipitation reaction. Washed immunoprecipitates were incubated in 50 μl of buffer containing 20 mM Tris, 5 mM MgCl2, 5 mM MnCl, μM ATP, and 200 μCi/ml 32P-ATP (Amersham Corp.). The reaction was carried out for 15 minutes at 25° C. and was terminated by the addition of ice cold wash buffer. After washing the beads again, the reaction products were eluted, electrophoresed and autoradiographed.
A phosphorylated polypeptide having the expected 125 kDa molecular weight was evident in immunoprecipitates from NK cells but not in immunoprecipitates from resting T-cells or untreated control cells. The phosphorylated residues were resistant to KOH, consistent with tyrosyl phosphorylation. We concluded that this tyrosyl phosphorylation likely represented autophosphorylation of JAK-3.
Thus, our results indicated the novel JAK-3 protein had both structural and functional characteristics of a protein tyrosine kinase related to the Janus family of PTK. In an effort to discern the role of JAK-3 in cellular physiology, we made a more extensive investigation into the range of cell types that expressed the JAK-3 protein.
Example 6 describes the method used to determine the range of cell types that express JAK-3 protein.
Whole cell lysates from human peripheral blood T-cells (unstimulated or stimulated for 48 hours with PHA), the transformed T-cell lines Hut78 and YT, peripheral blood NK cells, the NK 3.3 cell line, human peripheral blood monocytes, the myelomonocytic cell lines U937 and THP-1, and the tumor cell line OVCAR-3, HT-29 and IM-9 were run on SDS-PAGE and were probed with antisera to JAK-3. Human peripheral blood T lymphocytes, NK cells and monocytes (>97% pure) were obtained by leukophoresis and column purification according to standard procedures. T lymphocytes were either untreated or treated with PHA (10 μg/ml) and incubated for 0-48 hours. Cells were grown in RPMI 1640 supplemented with calf serum. Cells were lysed in buffer containing TRITON™ X-100 detergent and clarified lysates (50 μg) were run on SDS PAGE, transferred to IMMOBILON™ membrane and probed with anti-JAK-3 antisera and HRP-conjugated antirabbit immunoglobulin. Immunoblots were developed with enhanced chemiluminescence (Amersham) using standard procedures. The anti-JAK-3 antiserum used in these procedures was raised against a synthetic peptide corresponding to the C-terminal region of the JAK-3 protein (amino acids 1104-1124), and has been described by Kawamura et al., in Proc. Natl. Acad. Sci. USA 91:6374 (1994).
The results from these procedures indicated that JAK-3 was expressed only in a limited spectrum of tissue types. It was strongly expressed in NK cells, the NK cell line NK 3.3, YT cells and in the transformed T-cell line Hut78 as judged by the presence of a 125 kDa band on the Western blot. The JAK-3 protein was not detected in other cell types that were examined. In contrast to the pattern of JAK-3 protein expression, other JAK family kinases are known to be expressed in both lymphoid and nonlymphoid cells. While JAK-3 was expressed at low levels in resting peripheral blood T-cells, these levels of expression were greatly increased following activation by either PHA or anti-CD3.
The induction of the IL-2 gene and IL-2 receptor a chain are among the critical events that occur during T-cell activation. These factors have been considered by Taniguchi in Ann. Rev. Immunol. 4:69 (1988), and by Leonard et al., in Proc. Natl. Acad. Sci. USA 80:6957 (1983). As the induction of these genes paralleled the induction of JAK-3, we investigated the possibility that JAK-3 was somehow coupled to the IL-2 receptor. Indeed, in Cell 74:587 (1993), Stahl et al. disclosed that occupancy of certain other cytokine receptors induced tyrosine phosphorylation of other JAKs.
Example 7 describes the methods used to demonstrate that the JAK-3 protein is inducibly phosphorylated by IL-2 stimulation of T and NK cell lines, and peripheral blood NK cells.
Cells were either unstimulated or stimulated with IL-2 (1000 U/ml) for 5 minutes, then lysed, immunoprecipitated with anti-JAK-3 antisera and immunoblotted and probed with a monoclonal antiphosphotyrosine antibody (4G10 UBI). In this procedure, cells were washed twice with RPMI that had been acidified at pH 6.5 before incubation for 3 hours with 0.5% human serum. The cells were again washed twice before stimulation with IL-2. The cells were lysed in buffer containing TRITON™ X-100 detergent prior to the immunoprecipitation procedure. Detection of the antiphosphotyrosine antibody probe bound to the 125 kDa JAK-3 protein band was by autoradiography.
Using this procedure, we found that IL-2 induced tyrosine phosphorylation of JAK-3 in YT (T-cell line) and NK 3.3 (NK cell line) cells as well as in peripheral blood NK cells. We observed little basal tyrosine phosphorylation of JAK-3 in any of the cell samples that were tested. However, after 5 minutes of IL-2 stimulation, intense phosphorylation of a protein band having a molecular weight of 125 kDa was evident on the autoradiograph. This band represented the JAK-3 protein. A constitutively expressed phosphoprotein band that migrated at a discrete position in the gel between the 69 and 96 kDa molecular weight markers was observed in YT and NK3.3 cell lines, and in peripheral blood NK cells. A second constitutive phosphoprotein band was observed in the NK3.3 lanes on the autoradiograph. In aggregate, these results indicated that JAK-3 is a protein that is inducibly phosphorylated by stimulation of T-cells and NK cells with IL-2.
IL-2 induced tyrosine phosphorylation in the Hut78 T-cell line was also examined in a time course experiment. Lysates from Hut78 cells either untreated or treated with IL-2 for 5, 10 or 30 minutes were immunoprecipitated with anti-JAK-3 and blotted with antiphosphotyrosine antibody and with anti-JAK-3. Our results indicated that Hut78 cells showed induction of JAK-3 tyrosine phosphorylation after treatment with IL-2 that was maximal at 10 minutes. Prior absorbance of the JAK-3 antiserum with cognate peptide eliminated the tyrosine phosphorylated protein at 125 kDa and thereby confirmed the specificity of the tyrosine phosphorylated band as JAK-3. JAK-3 was also found to be phosphorylated in response to IL-2 in human peripheral blood T-cells that had been pre-activated with PHA for 24 hours. Thus in human T and NK cells, T-cell and NK cell lines, IL-2 induced the rapid tyrosyl phosphorylation of JAK-3 protein.
Both Farrar, et al. (J. Biol. Chem. 264:12,562 (1989)) and Kirken, et al., (J. Biol Chem. 268:22,765 (1993)) have disclosed that IL-2 stimulation induced tyrosyl phosphorylation of a variety of substrates in human peripheral blood T-cells and T-cell lines. In the following Example, we demonstrated that the most prominent phosphotyrosyl protein evident following IL-2 stimulation of the YT cell line was a polypeptide of 125 kDa that comigrated with JAK-3. To confirm the identity of this 125 kDa substrate as JAK-3, an experiment was conducted in which lysates from IL-2 treated cells were first depleted of JAK-3 prior to immunoprecipitation with antiphosphotyrosine antibodies. In addition, we examined whether the other JAK family members could be activated by IL-2.
Example 8 describes the methods used to demonstrate that JAK-1 and JAK-3 are tyrosine phosphorylated in T-cells upon IL-2 stimulation.
Serum-starved YT cells were treated with IL-2 (1000 U/ml) for 0 or 15 minutes. Cells were lysed in buffer containing TRITON™ X-100 detergent and phosphatase inhibitors and then immunoprecipitated with an antiphosphotyrosine antibody bound to protein G sepharose. Lysates were precleared with either rabbit polyclonal antisera, anti-JAK-3 or anti-JAK-1 before immunoprecipitation and immunoblotting with anti-phosphotyrosine. As a positive control to identify the position of JAK-3 on the Western blot, a sample of the lysate from IL-2 induced cells was immunoprecipitated with anti-JAK-3 and blotted with antiphosphotyrosine. All immunoprecipitates were subjected to SDS-PAGE and transferred to IMMOBILON™ membrane.
Depletion of YT cell lysates with anti-JAK-3 antiserum specifically removed the 125 kDa tyrosine phosphorylated protein, thus indicating that JAK-3 was one of the most prominent phosphoproteins detected in response to IL-2 in these cells. Conversely, depletion of lysates with anti-JAK-1 did not remove this phosphoprotein. This result clearly established that JAK-3 is a prominent tyrosyl phosphoprotein in IL-2 induced T-cells.
In addition, we examined whether other JAK family members could be activated by IL-2. An experiment similar to that described above was performed in which antiphosphotyrosine immunoblots were purposely overexposed to reveal other substrates. In particular, YT cells were treated with IL-2 (1000 U/ml) for 0, 5 or 15 minutes, lysed, immunoprecipitated with anti-phosphotyrosine and subsequently immunoblotted with anti-phosphotyrosine, and anti-JAK-3 or anti-JAK-1. We observed a tyrosyl phosphoprotein induced in response to IL-2 that was larger in size than JAK-3. Immunoprecipitation with anti-JAK-1 antiserum and immunoblotting with antiphosphotyrosine confirmed that this protein was JAK-1. Although both Tyk2 and JAK-2 could be detected in YT cells, no tyrosyl phosphorylation of either protein was observed in response to IL-2 stimulation.
Thus, the results obtained in Example 8 indicated that IL-2 stimulation of T-cells led to tyrosine phosphorylation of JAK-3 and, to a somewhat lesser extent, of JAK-1.
Example 9 describes the methods used to demonstrate that IL-2 stimulates JAK-3 in vitro kinase activity.
Cells were treated with IL-2 (1000 U/ml) for 0, 10 or 20 minutes. In vitro kinase activity was measured in anti-JAK-3 immunoprecipitates. For measurement of in vitro kinase activity, immunoprecipitates were washed in 50 mM NaCl, 5 mM MgCl2, 5 mM MnCl2, 0.1 mM Na3VO4, 10 mM HEPES (pH 7.4) and incubated in the same buffer containing 0.25 μCi/ml [32P-γ] ATP for 15 minutes at room temperature. After three washes, proteins were eluted in sample buffer and analyzed by SDS-PAGE. Gels were either dried or transferred to IMMOBILON™ membrane before exposure. Autophosphorylation signals were detected by autoradiography of the dried gels. JAK-3 in vitro kinase activity in response to IL-2 stimulation (15 minutes) was measured in immunoprecipitates from peripheral blood NK cells and Hut78 cells. JAK-3 immunoprecipitated from YT cells activated in response to IL-2 displayed elevated kinase activity that peaked at approximately 10 minutes. Similar results were obtained using human peripheral blood NK cells and Hut78 cells. This kinase activity was not precipitated by preimmune serum or in the presence of competing JAK-3 peptide. These results confirmed that the observed kinase activity was specific for the JAK-3 protein. The vast majority of the phosphorylation observed was attributable to phosphorylation of tyrosine residues as demonstrated by resistance to KOH treatment and by phosphoamino acid analysis.
We next examined JAK-3 phosphorylation in YT cells following stimulation by a number of these cytokines Other members of the JAK family have been shown to be activated by several lymphokines including the interferons (IFNs), erythropoietin (EPO), growth hormone (GH) and IL-3 (Witthuhn et al., Cell 74:227 (1993); Argetsinger et al., Cell 74:237 (1993); Silvennoinen et al., Proc. Natl. Acad. Sci. USA 90:8429 (1993)). JAK-3 was tyrosine phosphorylated in response to IL-2, but not in response to GH, IFN-α or IFN-γ in the YT cells. We did detect tyrosine phosphorylation of JAK-2 in response to IFN-γ in these cells, thus confirming the activity of this cytokine. Stimulation of YT cells with IL-3, GM-CSF or EPO also failed to induce JAK-3 phosphorylation. IL-4 has recently been shown to utilize the common y chain of the IL-2 receptor (γc), suggesting that common signaling pathways also may be utilized by these cytokines (see Russell et al., Science 262:1880 (1993), and Kondo et al., Science 262:1874 (1993)). This knowledge prompted us to examine whether JAK-3 was also activated in response to IL-4.
Example 10 describes the methods used to test whether other cytokines, in addition to IL-2, induced JAK-3 tyrosine phosphorylation.
YT cells were serum-starved for 3 hours and acid washed twice before stimulation and immunoprecipitation. NK 3.3 cells were grown for 2 days in 10% lymphocult (Biotest) and 15% fetal bovine serum before being washed and incubated in 2% serum. Commercial polyclonal anti-JAK-1 and JAK-2 antisera were obtained from UBI and Tyk2 polyclonal antiserum from Santa Cruz Biotechnology.
Lysates of YT cells that were unstimulated or stimulated with IL-2 (1000 U/ml), GH (50 ng/ml), IFN-α (1000 U/ml) or IFN-γ (500 U/ml) for 15 minutes were immunoprecipitated with anti-JAK-3 and blotted with antiphosphotyrosine. Results from this Western blotting experiment proved that JAK-3 was tyrosine phosphorylated in response to IL-2, but not in response to GH, IFN-α or IFN-γ. In addition, JAK-3 was not phosphorylated in response to IL-3, granulocyte macrophage colony stimulating factor (GM-CSF) or erythropoietin, all of which have been shown to activate JAK-2.
In related procedures, NK 3.3 cells that were incubated overnight in 2% serum were stimulated with IL-2 (1000 U/ml), IL-4 (100 U/ml) or IFN-γ (500 U/ml) for 5 or 15 minutes. Cellular lysates were immunoprecipitated with anti-JAK-3 and blotted with antiphosphotyrosine. Results from these procedures indicated that JAK-3 was tyrosine phosphorylated in response to both IL-4 and IL-2 in NK 3.3 cells. These results confirmed that the JAK-3 kinase is involved in signaling pathways other than IL-2.
Given these findings, we proceeded to investigate the detailed mechanism by which the JAK proteins were involved in IL-2 mediated signal transduction. As described in the following Examples, we discovered that two of the IL-2 receptor subunits interacted with the JAKs. In particular, we discovered that the JAK-1 and JAK-3 proteins physically interacted with the IL-2Rβ and γc IL-2 receptor subunits. Further, the γc-JAK-3 binding was found to be induced by IL-2 stimulation. Our procedures began with a demonstration that both the JAK-1 and JAK-3 proteins are phosphorylated by IL-2 stimulation.
Example 11 describes methods that can be used to detect phosphorylation of the JAK-1 and JAK-3 proteins.
Peripheral blood lymphocytes (PBL) were induced for 15 minutes with IL-2 (1000 U/ml), IL-4 (100 U/ml), IL-7 (100 ng/ml), or IL-9 (100 ng/ml) after phytohemagglutinin (PHA) stimulation. The PBL were activated for 72 hours with PHA, then washed twice at pH 6.5, incubated for 3 hours in medium containing 0.5% human serum and resuspended in medium containing 10% fetal calf serum for one hour. Cells were then lysed and immunoprecipitated with polyclonal antibodies to JAK-1 (UBI) or JAK-3. The anti-JAK-3 antibody used in these procedures has been described by Johnston et al., in Nature 370:151 (1994). Phosphotyrosine-containing proteins were detected by immunoblotting with 4G10 (UBI). NK3.3 cells were stimulated with IFN-α (1000 U/ml) or IL-2 (1000 U/ml), immunoprecipitated with polyclonal antibodies to Tyk2 (UBI) or JAK-2 (UBI) and immunoblotted with 4G10 mAb to phosphotyrosine (UBI). In one procedure, the lysate was precleared with polyclonal antibody to JAK-3.
Although immunoprecipitation with antibodies to JAK-2 yielded a tyrosine phosphorylated band in response to IL-2, this band migrated faster than the JAK-2 band induced by interferon-γ and was human JAK-3, immunoprecipitated through cross-reactivity with the JAK-2 antiserum. This was demonstrated by elimination of this band by preclearing the lysate with a JAK-3 specific antiserum. In addition to IL-2, we tested three other known γc users, IL-4, IL-7 and IL-9, for their abilities to induce the tyrosine phosphorylation of JAK-1 and JAK-3. Each of these cytokines induced tyrosine phosphorylation of both JAK-1 and JAK-3 in Western blotting procedures and activated both JAK-1 and JAK-3 as evaluated by in vitro kinase assays. Thus, cytokines that signal using mechanisms that involve the common γc subunit induce phosphorylation of JAK-1 and JAK-3.
Given the essential roles of both IL-2Rβ and γc in IL-2 signal transduction, we investigated the ability of each of these chains to physically associate with JAK-1 and/or JAK-3, the two Janus kinases that were activated and tyrosine phosphorylated in response to IL-2. YT cellular lysates were immunoprecipitated with Mikβ1 (anti-IL-2Rβ) monoclonal antibody (mAb) or R878 (anti-γc) antiserum, followed by Western blotting with JAK-3 and reblotting with JAK-1.
Example 12 describes the methods used to demonstrate that JAK-1 binds the IL-2Rβ subunit, and that JAK-3 binds the γc subunit of the IL-2 receptor.
YT cells were either stimulated or not stimulated with IL-2 and then lysed with 10 mM Tris (pH 7.5) containing 2 mM EDTA, 0.15 M NaCl, 0.875% Brij 96, 0.125% NONIDET P40™ detergent, 0.4 mM sodium vanadate, 1 mM 4-(2-aminoethyl)-benzenesulfonyl fluoride hydrochloride (ICN), 2.5 mM leupeptin, 2.5 mM aprotinin. Immunoprecipitations were performed using Mikβ1 anti-IL-2Rβ mAb, R878 antiserum to γc, or RPC5 (control mAb). The gel was Western blotted sequentially with antisera to JAK-3 and then JAK-1 using ECL. The object of this coprecipitation procedure was to test whether precipitation of one subunit of the IL-2 receptor would also precipitate one of the JAK proteins.
Our results indicated that JAK-1 constitutively associated with IL-2Rβ, and that the quantitative extent of association did not increase following IL-2 stimulation. JAK-1 did not constitutively associate with γc, but after IL-2 stimulation and the induction of association of IL-2β with γc, some JAK-1 coprecipitated with γc. Although JAK-3 weakly associated with γc in the absence of IL-2, this association increased following IL-2 stimulation. Moreover, after IL-2 stimulation, JAK-3 was readily coprecipitated with anti-IL-2Rβ mAb Mikβ1 or TU11. This was expected for TU11, which binds to an IL-2Rβ epitope distinct from the IL-2 binding site and coprecipitates γc in the presence but not absence of IL-2, but was unexpected for Mikβ1, which competes for IL-2 binding and cannot coprecipitate γc in the presence or absence of IL-2.
These data indicated that IL-2Rβ primarily associated with JAK-1 and that γc associated with JAK-3. However, interactions between IL-2Rβ and JAK-3 also occurred. Though the basis for the IL-2 induced association of IL-2Rβ with JAK-3 is unknown, IL-2 induced heterodimerization of IL-2Rβ and γc may juxtapose JAK-3 to IL-2Rβ, thus facilitating their interaction. Significantly, the association of JAK-3 with γc was induced by IL-2.
To further evaluate the association of IL-2Rβ and γc with JAK-1, we transiently transfected COS-7 cells with cDNAs encoding JAK-1 and either IL-2Rβ or γc.
Example 13 describes a cotransfection procedure that confirmed the physical interaction between JAK-1 and IL-2Rβ. The results of this procedure did not provide evidence for an interaction between JAK-1 and the γc receptor subunit.
Cotransfection of COS-7 cells with JAK-1 and either IL-2Rβ or γc expression constructs was followed by immunoprecipitation and Western blotting with Erd A antiserum to IL-2Rβ, R878 antiserum to γc or antiserum to JAK-1. The IL-2Rβ expression construct used in this procedure consisted of the IL-2Rβ1 cDNA insert described by Gnarra et al., in Proc. Natl. Acad. Sci. USA 87:3440 (1990), under transcriptional control of the SRα promoter that has been described by Takebe et al., in Mol. Cell. Biol. 8:466 (1988). The γc expression construct used in this procedure included a γc cDNA insert derived from a clone that was isolated from a cDNA library prepared from YT cell mRNA. The 5′ end of the γc cDNA insert corresponded to position −43 as presented in FIG. 2 by Noguchi et al., in J. Biol. Chem. 268:13601 (1993), and extended to the 3′ end of the full length γc sequence that has been presented by Takeshita et al., in Science 257:379 (1992). The JAK-1 expression construct used in this procedure had the JAK-1 cDNA under transcriptional control of the CMV promoter. When JAK-1 and IL-2Rβ expression constructs were cotransfected, antibodies to either protein coprecipitated the other as evaluated by Western blotting. As expected, the RPC5 control mAb failed to immunoprecipitate material that could be identified by either the anti-JAK-1 or the anti-IL-2Rβ antiserum on the Western blot. This negative result confirmed the specificity of the blotting procedure. The Gnarra et al., Takebe et al., Noguchi et al., and Takeshita et al. references referred to in this example are all incorporated herein by reference.
Our results also indicated that γc and JAK-1 did not associate with each other. This latter finding was evidenced by the inability of anti-JAK-1 to immunoprecipitate material that could be stained on Western blots probed with anti-γc antibodies, and by the inability of anti-γc to immunoprecipitate material that could be stained on Western blots probed with anti-JAK-1. On the other hand, anti-JAK-1 immunoprecipitated material that was stained by anti-JAK-1, and anti-γc antibodies immunoprecipitated material that was stained by anti-γc antibodies. This latter observation confirmed the integrity of the reagents used in these procedures. As expected, the RPC5 control mAb failed to immunoprecipitate material that was stained by either anti-JAK1 or anti-IL-2Rβ antiserum on the Western blot. Although the positive control procedures confirmed our ability to detect all relevant protein species, we did not obtain any evidence for an association between JAK-1 and the γc receptor chain. However, these findings did confirm a physical association between JAK-1 and IL-2Rβ.
We conducted an experiment to determine the relative importance of the cytoplasmic domain of the IL-2Rβ receptor chain, and to test the importance of the extracellular domain with respect to facilitating the interaction between JAK-1 and the IL-2Rβ chain. COS-7 cells were cotransfected with JAK-1 and either IL-2Rα, chimeric α/α/β or chimeric α/γ/65 expression constructs according to standard protocols. The structures of the chimeric constructs encoding these novel receptor chains has been described by Nakamura et al., in Nature 369:330 (1994), the disclosure of which is hereby incorporated by reference. The RPC5 control mAb and anti-Tac mAb to IL-2Rα were separately used for immunoprecipitations that were followed by Western blotting with antiserum to JAK-1. Neither anti-Tac nor RPC5 antibodies immunoprecipitated material from lysates of JAK-1 and IL-2Rα cotransfectants that was also stained by anti-JAK-1. Thus, there was no evidence that JAK-1 interacted with any portion of the IL-2Rα chain. Neither anti-Tac nor RPC5 antibodies immunoprecipitated material from lysates of JAK-1 and chimeric α/γ/65 cotransfectants that was also stained by anti-JAK-1. Thus, there was no evidence that JAK-1 interacted with the cytoplasmic portion of the γc receptor chain. On the other hand, when lysates from cells cotransfected with JAK-1 and chimeric α/α/62 were immunoprecipitated with anti-Tac and Western blotted, material stained by anti-JAK-1 was detected.
These results established that recombinant components of the IL-2 receptor associate with each other in defined ways. Further, our results confirmed the interaction of the JAK-1 and IL-2Rβ proteins, and indicated that the cytoplasmic portion of the IL-2Rβ chain was required for this interaction.
We next used transfected COS-7 cells to evaluate the association of JAK-3 with γc mutants in order to identify regions of contact between the JAK-3 and γc proteins. These coprecipitation experiments employed two different anti-γc antibodies, a monoclonal antibody that recognized the extracellular domain of γc, and R878, a polyclonal antiserum that recognized the intracellular domains of γc. As described below, we discovered that recombinant γc and JAK-3 proteins efficiently interacted with each other. In contrast, two truncated forms of the receptor chain in which either 80 or 48 amino acids had been deleted from the C-terminus (Russell et al. Science 262:1880 (1993)) exhibited greatly diminished association with JAK-3. The 48 amino acid truncation is smaller than the truncation found in the XSCID patient with the smallest known naturally occurring γc truncation (missing 62 amino acids). Other XSCID patients have been identified with even larger truncations. Thus, the findings presented below confirmed that the inability of JAK-3 to associate with γc would be a characteristic of many XSCID patients.
Example 14 describes experiments which demonstrated recombinant γc chains that incorporate mutations similar to those found in XSCID patients cannot efficiently associate with JAK-1.
COS-7 cells were transfected with JAK-3 and either wild type γc or γc-ΔCT, γc-ΔSH2, γ2-L271Q or with the vector control (pME18S). The γc expression construct used in these procedures is described under Example 13. The γc-ΔCT and γc-ΔSH2 constructs were prepared as described by Russell et al., in Science 262:1880 (1993). The γc-L271Q expression construct was prepared by using the pAlter-1 Mutagenesis Vector system (Promega), and is essentially identical to the wild type γc construct, except for mutation of codon 271 from CTG to CAG. The transfectants were lysed and immunoprecipitated with the extracellular domain-recognizing antibody or R878 anti-γc antibodies and Western blotted with JAK-3 antiserum. Expression of transfected wild type and mutant γc constructs were similar as determined by flow cytometry. Note that whereas the extracellular domain-recognizing antibody mAb bound to an extracellular epitope and thereby all the mutant forms of γc tested, R878 cannot bind γc-ΔCT or γc-ΔSH2 truncation mutants which lack the critical epitope.
The extracellular domain-recognizing antibody immunoprecipitates from cells cotransfected with JAK-3 and wild type γc contained material that was Western blotted with anti-JAK-3. No other cotransfectant gave similar results. Repetition of the procedure using the R878 anti-γc immunoprecipitates gave essentially similar results, except that a small amount of anti-JAK-3 staining material was observed in the lane corresponding to the lysate from cells that had been cotransfected with JAK-3 and γc-L271Q expression constructs. We noted that the amount of JAK-3 associating with γc-L271Q was substantially less than the amount of JAK-3 associating with the wild type γc. These results indicated that mutation of the amino acid at position 271 of the γc chain inhibited JAK-3 binding. This implicated the region of the γc protein that included amino acid position 271 as being critical for interaction with the JAK-3 protein.
Neither the vector control nor any of the γc mutants that were tested in our experiments gave any indication for JAK-3 binding. Further, we discovered that the portion of the γc chain that included amino acid position 271 represented a critical domain of the protein that was required for JAK-3 binding.
We have recently characterized the genetic defect in a pedigree with an X-linked combined immunodeficiency as a single nucleotide change within the γc cytoplasmic domain, resulting in replacing Leu 271 with Gln. As described above, the γc-L271Q mutation significantly diminished but did not abrogate association with JAK-3. The finding that the γc-L271Q mutant still weakly associated with JAK-3 was consistent with the disease phenotype in this pedigree being less severe than typical XSCIDs. Nevertheless, affected males manifest diminished and retarded development of CD4+ and CD8+ T-cells and decreased T-cell responses to mitogens and IL-2.
Interestingly, Leu 271 is not contained within the region deleted in the γc-ΔSH2 mutant. We interpret this as indicating that JAK-3 may contact residues both proximal and distal to the deletion point in the γc-ΔSH2 construct. An experiment described in Example 15, that was conducted using a 19 amino acid long peptide spanning Leu 271, supports this hypothesis since the peptide only partially inhibited γc-JAK-3 coprecipitation, even when present at high molar excess. When IL-2Rβ and JAK-3 were cotransfected into COS-7 cells, Mikβ1 anti-IL-2Rβ mAb weakly but reproducibly coprecipitated JAK-3.
As described above, we have disclosed that JAK-3 is indeed the kinase that associates with γc and that JAK-3 is activated and tyrosine phosphorylated by all previously known γc users tested, as well as IL-9, which we now add to the list of known γc users. Moreover, we have partially defined the regions and residues of γc required for JAK-3 association and correlated defective γc-JAK-3 association with XSCID.
The activation of JAK-1 by IL-2, IL-4, IL-7, and IL-9 was an unexpected result and suggests that IL-4R, IL-7R, and IL-9R, like IL-2Rβ, all associate with JAK-1. We have recently shown that IL-15 also activates JAK-1 and JAK-3. The activation of JAK-1 and JAK-3 presumably is vital to signal transduction mediated by IL-2, IL-4, IL-7, IL-9 and IL-15. However, it is clear that the distinct signals transduced by different γc users cannot be explained solely by JAK-1 and JAK-3. Unique actions, such as the induction of tyrosine phosphorylation of IRS-1 by IL-4, presumably play major roles in determining cytokine-specific actions, and may reflect the abilities of specific receptor complexes to recruit different substrates for the activated JAKs or other kinases.
Finally, we contemplate that the discoveries described above can be used to design assays for identifying compounds that inhibit IL-2 dependent signaling. Specifically, we contemplate that compounds that disrupt the interaction between JAK-1 and the IL-2Rβ subunit, or between JAK-3 and the γc subunit of the IL-2 receptor will be potential inhibitors of IL-2 signalling. The descriptions provided in the foregoing Examples detail how interactions between the JAK kinases and the IL-2Rβ and γc chains of the receptor can be detected. Contemplated inhibitors will be identified by virtue of inhibiting these interactions.
To illustrate how an inhibitor can be identified according to the invented method, we have conducted experiments using a synthetic peptide as a model inhibitor to inhibit the interaction between γc and JAK-3 in vitro. Specifically, the peptide used in this procedure had an amino acid sequence corresponding to a portion of the γc chain that binds the JAK-3 protein. The assay employed standard immunoprecipitation and Western blotting methods. In the following exemplary case, the γc synthetic peptide prevented binding of wild type γc to JAK-3. Since the anti-γc antibody used in the immunoprecipitation procedure did not immunoprecipitate the complex between the γc synthetic peptide and the JAK-3 protein, inhibition of γc binding to JAK-3 was determined by virtue of the ability of the synthetic peptide to inhibit coprecipitation of the complex containing γc and JAK-3. Significantly, the fact that a negative control peptide failed to inhibit the interaction between γc and JAK-3 demonstrated the specificity of the inhibition. Thus, the assay described below clearly distinguished between agents that did and agents that did not inhibit the γc-JAK-3 interaction.
Example 15 describes an assay that can be used to identify compounds that inhibit IL-2 receptor activation by preventing the interaction between JAK-3 and the γc chain.
YT cells or COS-7 cells expressing γc and JAK-3 were stimulated or not stimulated with IL-2 and then lysed with 10 mM Tris (pH 7.5) containing 2 mM EDTA, 0.15 M NaCl, 0.875% Brij 96, 0.125% NONIDET P40™ detergent, 0.4 mM sodium vanadate, 1 mM 4-(2-aminoethyl)-benzenesulfonyl fluoride hydrochloride (ICN), 2.5 mM leupeptin, 2.5 mM aprotinin. The peptide to be tested as an inhibitor corresponded to the first 19 amino acids of the γc cytoplasmic tail (sequence ERTMPRIPTLKNLEDLVTE) (SEQ ID NO:7). A negative control peptide that was not expected to inhibit the interaction between γc and JAK-3 corresponded to a tyrosine phosphorylated region of γc. The negative control peptide had the sequence APPCYTLKPET (SEQ ID NO:10), and was synthesized so that the Tyr residue at position 5 of the peptide was phosphotyrosine. The test peptide or the negative control peptide were separately added to the cell lysates to final concentrations of 140 μM. The positive control immunoprecipitation was carried out in the absence of added peptide. Lysates were immunoprecipitated for 16 hours at 4° C. using antibodies to γc and protein A sepharose and washed six times before electrophoresis on SDS gels. The gels were immunoblotted with antisera to JAK-3 using ECL as described previously.
Results of the experiment described above indicated that only the competitor peptide partially inhibited γc-JAK-3 coprecipitation. As expected, and consistent with the findings presented under Example 12, only a weak association between the γc and JAK-3 proteins was observed in the absence of IL-2 stimulation.
In particular, the lane corresponding to the positive control coprecipitation in the extracts from IL-2 induced cells displayed an intense band on the x-ray film at a position corresponding to a molecular weight of 125 kDa. This result indicated the position of the JAK-3 protein on the immunoblot and provided a baseline for quantitative comparison with the test and negative control samples. The lane corresponding to the negative control sample had an intensity that was essentially identical to the band intensity in the positive control lane. This result indicated that the negative control peptide failed to inhibit association of γc and JAK-3 proteins. The lane corresponding to the sample containing the polypeptide being tested as an inhibitor had a band representing the JAK-3 protein that was of significantly diminished intensity. This result indicated that the 19 amino acid polypeptide having the sequence of SEQ ID NO:6 inhibited the γc-JAK-3 interaction. These findings illustrate the results that would be expected in assays for identifying inhibitors of the γc-JAK-3 interaction. In particular, an inhibitor of the yc-JAK-3 interaction can be identified by virtue of its ability to lessen the amount of the γc-JAK-3 coprecipitate compared to a trial that was conducted in the absence of any inhibitor.
Although the foregoing procedure was carried out by first immunoprecipitating with an anti-γc antibody and then Western blotting and probing with an anti-JAK-3 antibody, we anticipate the order of antibody usage could be reversed with equally good results. In particular, we anticipate that immunoprecipitation could be performed using the anti-JAK-3 antibody, and the Western blot probed with the anti-γc antibody. In this latter case, inhibitors of the γc-JAK-3 interaction would still be identified by virtue of diminishing the amount of γc-JAK-3 coprecipitate. The assay for inhibitors will involve identifying agents that cause a reduction in the amount of γc detected on the x-ray film relative to a trial that omitted the inhibitor.
Further, we anticipate that assays such as that described under Example 15 will be useful in the discovery of non-polypeptide drugs that inhibit the γc-JAK-3 interaction. These drugs will similarly be identified in such assays by virtue of their abilities to inhibit coprecipitation of the γc-JAK-3 complex.
Still further, we contemplate coprecipitation and Western blotting assays to identify compounds that inhibit the interaction between JAK-1 or JAK-3 and IL-2Rβ. Such assays can be readily performed using techniques well known to those having ordinary skill in the art. Inhibitors of this interaction are believed useful as drugs to inhibit transmembrane signalling that is dependent on the interaction between these receptor subunits. Specifically, these drugs are anticipated for use as immunomodulators which inhibit IL-2 dependent signalling.
This application is a divisional of U.S. patent application Ser. No. 12/354,668, filed Jan. 15, 2009, which is a divisional of 11/195,197, filed Aug. 1, 2005 (now U.S. Pat. No. 7,488,808, issued Feb. 10, 2009), which is a continuation of U.S. application Ser. No. 08/373,934, filed Jan. 13, 1995 (now U.S. Pat. No. 7,070,972, issued Jul. 4, 2006), each of which is hereby expressly incorporated by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12354668 | Jan 2009 | US |
| Child | 13041204 | US | |
| Parent | 11195197 | Aug 2005 | US |
| Child | 12354668 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 08373934 | Jan 1995 | US |
| Child | 11195197 | US |
