NOD2 Pathway Activation by MDP or Mycobacterium tuberculosis Infection Involves the Stable Polyubiquitination of Rip2
2007; Elsevier BV; Volume: 282; Issue: 50 Linguagem: Inglês
10.1074/jbc.m703079200
ISSN1083-351X
AutoresYibin Yang, Catherine Yin, Amit Kumar Pandey, Derek W. Abbott, Christopher M. Sassetti, Michelle A. Kelliher,
Tópico(s)Pediatric health and respiratory diseases
ResumoThe Rip2 kinase contains a caspase recruitment domain and has been implicated in the activation of the transcriptional factor NF-κB downstream of Toll-like receptors, Nod-like receptors, and the T cell receptor. Although Rip2 has been linked to Nod signaling, how Nod-Rip2 proteins mediate NF-κB activation has remained unclear. We find Rip2 required for Nod2-mediated NF-κB activation and to a lesser extent mitogen-activated protein kinase activation. We demonstrate that Rip2 and IκB kinase-γ become stably polyubiquitinated upon treatment of cells with the NOD2 ligand, muramyl dipeptide. We also demonstrate a requirement for the E2-conjugating enzyme Ubc13, the E3 ubiquitin ligase Traf6, and the ubiquitin-activated kinase Tak1 in Nod2-mediated NF-κB activation. Rip2 polyubiquitination is also stimulated when macrophages are infected with live Mycobacterium tuberculosis but not when infected with heat-killed bacteria. Consistent with our data linking Rip2 to NOD and not Toll-like receptor signaling, M. tuberculosis-induced Rip2 polyubiquitination appears MyD88-independent. Collectively, these data reveal that the NOD2 pathway is ubiquitin-regulated and that Rip2 employs a ubiquitin-dependent mechanism to achieve NF-κB activation. The Rip2 kinase contains a caspase recruitment domain and has been implicated in the activation of the transcriptional factor NF-κB downstream of Toll-like receptors, Nod-like receptors, and the T cell receptor. Although Rip2 has been linked to Nod signaling, how Nod-Rip2 proteins mediate NF-κB activation has remained unclear. We find Rip2 required for Nod2-mediated NF-κB activation and to a lesser extent mitogen-activated protein kinase activation. We demonstrate that Rip2 and IκB kinase-γ become stably polyubiquitinated upon treatment of cells with the NOD2 ligand, muramyl dipeptide. We also demonstrate a requirement for the E2-conjugating enzyme Ubc13, the E3 ubiquitin ligase Traf6, and the ubiquitin-activated kinase Tak1 in Nod2-mediated NF-κB activation. Rip2 polyubiquitination is also stimulated when macrophages are infected with live Mycobacterium tuberculosis but not when infected with heat-killed bacteria. Consistent with our data linking Rip2 to NOD and not Toll-like receptor signaling, M. tuberculosis-induced Rip2 polyubiquitination appears MyD88-independent. Collectively, these data reveal that the NOD2 pathway is ubiquitin-regulated and that Rip2 employs a ubiquitin-dependent mechanism to achieve NF-κB activation. Conserved structures on pathogens are recognized by specific host receptors such as Toll-like receptors (TLRs) 2The abbreviations used are:TLRToll-like receptorCARDcaspase recruitment domainJNKc-Jun N-terminal kinaseNODnucleotide binding oligomerization domainNLRNOD-like receptorMAPmitogen-activated proteinMAPKMAP kinaseHAhemagglutininMDPmuramyl dipeptideTNFtumor necrosis factorILinterleukinsiRNAshort interfering RNAIKKIκB kinaseLPSlipopolysaccharideshRNAshort hairpin RNA. 2The abbreviations used are:TLRToll-like receptorCARDcaspase recruitment domainJNKc-Jun N-terminal kinaseNODnucleotide binding oligomerization domainNLRNOD-like receptorMAPmitogen-activated proteinMAPKMAP kinaseHAhemagglutininMDPmuramyl dipeptideTNFtumor necrosis factorILinterleukinsiRNAshort interfering RNAIKKIκB kinaseLPSlipopolysaccharideshRNAshort hairpin RNA. or nucleotide binding oligomerization domain (NOD)-like receptors (NLRs). In contrast to TLRs that recognize pathogens at the cell surface or within the endosome, NLRs induce innate immune responses by recognizing bacterial products released into the cytosol. Several NLRs, including Nod1 and Nod2 proteins, induce cytokine production by activating the transcription factor NF-κB and by stimulating MAP kinase activation (1Akira S. Takeda K. Nat. Rev. Immunol. 2004; 4: 499-511Crossref PubMed Scopus (6586) Google Scholar). The Nod1 protein recognizes a form of peptidoglycan containing the amino acid meso-diaminopimelic acid produced by Gram-negative and some Gram-positive bacteria (2Chamaillard M. Hashimoto M. Horie Y. Masumoto J. Qiu S. Saab L. Ogura Y. Kawasaki A. Fukase K. Kusumoto S. Valvano M.A. Foster S.J. Mak T.W. Nunez G. Inohara N. Nat. Immunol. 2003; 4: 702-707Crossref PubMed Scopus (1001) Google Scholar). The Nod2 pathway recognizes muramyl dipeptide (MDP) present on most types of peptidoglycan (3Inohara N. Ogura Y. Fontalba A. Gutierrez O. Pons F. Crespo J. Fukase K. Inamura S. Kusumoto S. Hashimoto M. Foster S.J. Moran A.P. Fernandez-Luna J.L. Nunez G. J. Biol. Chem. 2003; 278: 5509-5512Abstract Full Text Full Text PDF PubMed Scopus (1386) Google Scholar). Transfection studies have shown that expression of Nod proteins stimulates NF-κB activity, and the ability to stimulate NF-κB reporter activity is dependent on the co-expression of the adapter protein Rip2 (4Ogura Y. Inohara N. Benito A. Chen F.F. Yamaoka S. Nunez G. J. Biol. Chem. 2001; 276: 4812-4818Abstract Full Text Full Text PDF PubMed Scopus (1159) Google Scholar). Yet how Rip2 proteins achieve Nod-mediated NF-κBorMAP kinase activation remains undefined.Rip2 is a member of the Rip protein family of which there are currently seven members (5Meylan E. Tschopp J. Trends Biochem. Sci. 2005; 30: 151-159Abstract Full Text Full Text PDF PubMed Scopus (323) Google Scholar). Like the prototype Rip1, Rip2 contains an N-terminal serine threonine kinase domain followed by an intermediate region and a C-terminal caspase recruitment domain (CARD). Overexpression of Rip2 stimulates NF-κB activation and induces apoptosis, and expression of kinase-inactive Rip2 activates an NF-κB reporter, suggesting that the kinase activity of Rip2 may not be required for NF-κB activation upon stimulation of the Nod pathway (6McCarthy J.V. Ni J. Dixit V.M. J. Biol. Chem. 1998; 273: 16968-16975Abstract Full Text Full Text PDF PubMed Scopus (361) Google Scholar). To elucidate function, several groups generated Rip2-deficient mice and stimulated Rip2-deficient macrophages with TLR and NLR ligands. These studies concluded that Rip2 mediates NF-κB signals from multiple TLRs, NLRs, and from the T cell receptor (7Chin A.I. Dempsey P.W. Bruhn K. Miller J.F. Xu Y. Cheng G. Nature. 2002; 416: 190-194Crossref PubMed Scopus (330) Google Scholar, 8Kobayashi K. Inohara N. Hernandez L.D. Galan J.E. Nunez G. Janeway C.A. Medzhitov R. Flavell R.A. Nature. 2002; 416: 194-199Crossref PubMed Scopus (740) Google Scholar).We found Rip2 was required for Nod2 pathway activation in macrophages; however, we did not find Rip2 required for TLR2, -3, or -4-mediated IKK activation. Similar data have recently been published by Nunez and co-workers (9Park J.H. Kim Y.G. McDonald C. Kanneganti T.D. Hasegawa M. Body-Malapel M. Inohara N. Nunez G. J. Immunol. 2007; 178: 2380-2386Crossref PubMed Scopus (384) Google Scholar) who find Rip2 required for cytokine production induced through NLRs but not TLRs. We show that treatment of macrophages with the Nod2 ligand MDP stimulates the ubiquitin modification of endogenous Rip2 and IKK-γ. The ubiquitin modification of Rip2 is stable and involves the conjugation of Lys-63-linked polyubiquitin chains. MDP-induced Rip2 polyubiquitination and NF-κB activation require the E2-conjugating enzyme Ubc13, the E3 ubiquitin ligase Traf6, and the ubiquitin-activated kinase Tak1.The Nod2 pathway has been implicated in the innate immune response to Mycobacterium tuberculosis infection, as Nod2-deficient macrophages are impaired in their cytokine response to infection with M. tuberculosis (10Ferwerda G. Girardin S.E. Kullberg B.J. Le Bourhis L. de Jong D.J. Langenberg D.M. van Crevel R. Adema G.J. Ottenhoff T.H. Van der Meer J.W. Netea M.G. Plos Pathog. 2005; 1: 279-285Crossref PubMed Scopus (285) Google Scholar). Moreover, a quantitatively small fraction of the transcriptional changes induced by M. tuberculosis infection of macrophages can be attributed to TLR2/4- or MyD88-dependent pathways (11Shi S. Blumenthal A. Hickey C.M. Gandotra S. Levy D. Ehrt S. J. Immunol. 2005; 175: 3318-3328Crossref PubMed Scopus (80) Google Scholar). Collectively, these studies suggest nonredundant roles for NOD2 and TLR in the innate immune recognition of M. tuberculosis. We find that infection with live, but not heat-killed, virulent strains of M. tuberculosis stimulates Rip2 polyubiquitination. Therefore, we hypothesize that Nod proteins recognize M. tuberculosis components that are translocated into the cytosol, and consistent with this model, Rip2 polyubiquitination induced by live M. tuberculosis infection appears MyD88-independent, implicating NLRs in the cytosolic recognition of M. tuberculosis.EXPERIMENTAL PROCEDURESIsolation of Macrophages and M. tuberculosis Infection—To isolate peritoneal activated macrophages, wild type and rip2–/– mice (gift of Dr. Vishva M. Dixit, Genentech, Inc., South San Francisco) were injected with 3 ml of thioglycolate by intraperitoneal injection. Three days later, macrophages were isolated by gentle flushing of the peritoneal cavity. Peritoneal macrophages were left unstimulated or treated with MDP or purified LPS (Sigma). NF-κB activation was measured using phospho-IκBα antibodies (Cell Signaling Technology), p38 MAP kinase, and JNK1/2 activity was measured using anti-phospho-p38 and phospho-JNK1/2 antibodies (Cell Signaling Technology), respectively. Bone marrow-derived macrophages for M. tuberculosis infection were harvested from wild type or MyD88-deficient mice as described in Ref. 12Hise A.G. Daehnel K. Gillette-Ferguson I. Cho E. McGarry H.F. Taylor M.J. Golenbock D.T. Fitzgerald K.A. Kazura J.W. Pearlman E. J. Immunol. 2007; 178: 1068-1076Crossref PubMed Scopus (99) Google Scholar. M. tuberculosis (strain H37Rv) was cultivated in 7H9 broth to exponential phase and washed thoroughly in phosphate-buffered saline prior to infection. Bacterial clumps were removed by passing the washed suspension through a 5 μm syringe filter. "Heat-killed" bacteria were inactivated by heating to 80 °C for 30 min. Macrophages were infected for 1 or 2 h, after which filtered cell lysates were immunoprecipitated with anti-Rip2 antibody (Santa Cruz Biotechnology) or immunoblotted with anti-phospho-IκB-α antibody (Cell Signaling Technology).Plasmids and Constructs—The full-length Rip2 constructs were provided by Dr. Vishva M. Dixit (Genentech, South San Francisco). The wild type NOD2 construct has been described previously (13Abbott D.W. Wilkins A. Asara J.M. Cantley L.C. Curr. Biol. 2004; 14: 2217-2227Abstract Full Text Full Text PDF PubMed Scopus (314) Google Scholar). The HA-ubiquitin, HA-K48-only ubiquitin, and HA-Lys-63-only ubiquitin constructs were generously provided by Dr. Zhijan James Chen (University of Texas Southwestern, Dallas).Antibodies, siRNA, and Reagents—Anti-Rip2 (rabbit), anti-Nemo (rabbit), anti-Traf2 (rabbit), anti-Traf6 (mouse), anti-ubiquitin (mouse), anti-Omni (rabbit), anti-Tak1 (rabbit), anti-p38 (goat), and anti-JNK (rabbit) antibody were obtained from Santa Cruz Biotechnology. Anti-phospho-IκB-α, anti-phospho-p38, and anti-phospho-JNK antibodies were obtained from Cell Signaling Technology. Anti-UBC13 antibody was obtained from Zymed Laboratories Inc.; anti-FLAG and anti-β-actin antibody were obtained from Sigma, and anti-HA antibody was obtained from Roche Applied Science. Human Traf2 and Traf6 siRNA and mouse Tak1 siRNA were obtained from Santa Cruz Biotechnology. MDP was obtained from InvivoGen. Mouse TNF-α were obtained from Sigma. LPS derived from Escherichia coli strain 0111.B4 was purchased from Sigma, dissolved in deoxycholate, and re-extracted with phenol/chloroform as described in Ref. 14Hirschfeld M. Ma Y. Weis J.H. Vogel S.N. Weis J.J. J. Immunol. 2000; 165: 618-622Crossref PubMed Scopus (960) Google Scholar.Cell Culture, DNA Transfection, and siRNA Transfection—HEK293T cells and the mouse RAW 264.7 macrophage cell lines were obtained from ATCC and were grown in Dulbecco's modified Eagle's medium containing 10% fetal bovine serum. For all transfection studies, HEK293T cells were plated at 5 × 105 cells/plate on 60-mm plates. Constructs were transfected to HEK293T cells using FuGENE 6 transfection reagent (Roche Applied Science) according to the manufacturer's instructions. siRNAs were transfected to HEK293T cells using Lipofectamine 2000 (Invitrogen). Mouse control and Tak1-specific siRNAs were transiently transfected into the mouse RAW 264.7 macrophage cell line using a two-step transfection procedure and Lipofectamine 2000 (Invitrogen).Generation of Ubc13 Stably Knock Down RAW 246.7 Cell Lines—The mouse macrophage cell line RAW 264.7 was infected with lentiviruses containing shRNA sequences specific for Ubc13 (Open Biosystems) and selected with 2.5 μg/ml puromycin. Selected puromycin-resistant pools of cells were left unstimulated or treated with MDP, and Rip2 polyubiquitination was assayed by immunoprecipitation with anti-Rip2 antibody (Santa Cruz Biotechnology) followed by immunoblotting with anti-ubiquitin antibodies. The expression of the E2-conjugating enzyme Ubc13 in the lentiviral infected pools was determined by immunoblotting with an anti-Ubc13 antibody (Zymed Laboratories Inc.).Immunoprecipitation and Western Blot Analysis—For all immunoprecipitation and ubiquitination assays, cell lysates were prepared in radioimmune precipitation assay (RIPA) buffer (150 mm NaCl, 50 mm Tris-HCl (pH 7.5), 1% Nonidet P-40, 0.25% deoxycholate, 0.1% SDS, 1 mm EDTA), supplemented with a protease mixture inhibitor (Roche Applied Science) and 5 mm N-ethylmaleimide (Sigma), and immunoprecipitated with anti-Rip2 or anti-NEMO antibody (Santa Cruz Biotechnology). Polyubiquitinated Rip2 or NEMO/IKK-γ proteins were detected by immunoblotting with an anti-ubiquitin antibody (Santa Cruz Biotechnology). To examine endogenous protein interactions, cells were lysed in an endogenous lysis buffer (0.5 m Tris (pH 7.6), 0.5 m NaCl, 0.1 m EDTA, 1% Triton X-100, 0.5 m NaF, and 0.5 m sodium pyrophosphate) supplemented with a protease mixture inhibitor (Roche Applied Science), immunoprecipitated with anti-Rip2 antibody, and then immunoblotted with either anti-Tak1 or anti-Traf6 antibody (Santa Cruz Biotechnology). Expression of epitope-tagged, transfected proteins or endogenous proteins was detected by immunoblotting with corresponding antibodies.RESULTSThe CARD domain kinase Rip2 has been implicated in signaling from multiple TLRs, including TLR2, -3, and -4, the T cell receptor, and the cytosolic NOD1/2 pathways. To understand how Rip2 mediates such diverse signals, we isolated macrophages from Rip2-deficient mice and stimulated the cells with the NOD2 ligand muramyl dipeptide (MDP) or with purified LPS to stimulate the TLR4 pathway. We found that MDP and LPS induced NF-κB, p38 MAP kinase, and JNK1/2 activation when wild type macrophages were stimulated (Fig. 1A). Rip2-deficient macrophages also respond upon LPS stimulation but appear impaired in their ability to mediate NF-κB activation when treated with MDP (Fig. 1A). Similarly, the MDP-induced phospho-p38 and phospho-JNK1/2 activity was consistently impaired but not abrogated, suggesting that Rip2 contributes to MAP kinase activation but is not absolutely required (Fig. 1, A and B). These data suggest that Nod-mediated MAP kinase activation may involve other CARD domain containing adapter proteins. One possibility may be CARD9, as Card9-deficient mice exhibit defects in p38 MAP kinase and JNK activation in Nod-stimulated cells.We hypothesized that Nod-mediated IKK activation may involve the ubiquitin modification of Rip2 or IKK-γ/NEMO, and we tested this possibility by stimulating the mouse macrophage cell line RAW 264.7 with the Nod2 ligand MDP and assayed for the presence of polyubiquitinated Rip2 or NEMO/IKK-γ. We observed a ligand-dependent induction of Rip2 and NEMO/IKK-γ polyubiquitination, and interestingly, Rip2 polyubiquitination appears to precede the ubiquitin modification of NEMO/IKK-γ. Nod2 pathway activation by MDP appears to induce the stable modification of Rip2 and IKK-γ, suggesting that Rip2 and IKK-γ may be conjugated by Lys-63-linked polyubiquitin chains. To test this possibility, HEK293 cells were transfected with epitope-tagged versions of Rip2 and NOD2 in the presence of wild type or mutant forms of ubiquitin where only the lysine(s) at positions 63 or 48 are available for conjugation. In this setting, Rip2 appeared preferentially modified by Lys-63-linked polyubiquitin chains, and this activity appeared dependent on the presence of NOD2 (Fig. 2B). These data suggest that activation of the NOD2 pathway stimulates the stable Lys-63-linked polyubiquitination of Rip2.FIGURE 2NOD2 pathway activation stimulates the stable Lys-63-linked polyubiquitination of Rip2. A, MDP treatment stimulates the ubiquitin modification of endogenous Rip2 and NEMO/IKK-γ. The RAW 264.7 macrophage cell line was left untreated or treated with the NOD2 ligand MDP (10 μg/ml) for the indicated times. Cells were lysed, and an equal amount of total protein was immunoprecipitated (IP) with anti-Rip2 or anti-NEMO antibody (Santa Cruz Biotechnology). To detect ubiquitinated proteins, immunoprecipitated proteins were immunoblotted (IB) with an anti-ubiquitin (anti Ub) antibody (Santa Cruz Biotechnology). Total immunoprecipitated Rip2 or NEMO/IKK-γ protein was measured by immunoblotting with anti-Rip2 or anti-NEMO antibodies (Santa Cruz Biotechnology). B, NOD2 expression stimulates the stable, Lys-63-linked polyubiquitination of Rip2. Omni-tagged NOD2 and FLAG-tagged Rip2 constructs were expressed in HEK293T cells in the presence of HA-tagged Lys-63-only or HA-tagged K48-only forms of ubiquitin. Rip2 was immunoprecipitated with anti-Rip2 antibody (Santa Cruz Biotechnology), and Western blots were performed with the indicated antibodies. Expression levels of both FLAG-Rip2 and Omni-NOD2 were measured by immunoblotting total cell lysates with anti-FLAG or anti-Omni antibodies.View Large Image Figure ViewerDownload Hi-res image Download (PPT)Our studies suggest that NOD2-induced NF-κB activation may be mediated by the ubiquitin conjugation of Rip2 and IKK-γ, and the transfection studies suggest that Lys-63-linked polyubiquitin chains may stably modify both proteins. Therefore, we were interested in testing whether MDP-induced NF-κB activation and Rip2/IKK-γ polyubiquitination require expression of the E2-conjugating enzyme Ubc13, known to conjugate Lys-63-linked polyubiquitin chains. To address a requirement for Ubc13, we infected the MDP-responsive mouse macrophage cell line RAW 264.7 with lentiviruses expressing shRNAs specific for the Ubc13 enzyme. These stable pools of RAW 264.7 macrophages were impaired in their ability to phosphorylate IκBα in response to MDP or TNF-α (data not shown). Rip2 polyubiquitination was detected in RAW 264.7 macrophages expressing a control shRNA; however, treatment with the Nod2 ligand MDP failed to stimulate Rip2 polyubiquitination when the Ubc13-deficient cells were stimulated (Fig. 3A and not shown). The level of Rip2 polyubiquitination and MDP-induced NF-κB activation correlated with the reduction of Ubc13 expression achieved in the RAW 264.7 pools.FIGURE 3MDP-induced Rip2 polyubiquitination is dependent on the expression of the E2-conjugating enzyme Ubc13 and the E3 ubiquitin ligase Traf6. A, MDP fails to stimulate Rip2 polyubiquitination in Ubc13-deficient RAW 264.7 macrophages. The mouse macrophage cell line RAW 264.7 was infected with lentiviruses containing shRNA sequences specific for Ubc13 or green fluorescent protein as a control, and stable puromycin-resistant pools were selected. These lines were left untreated or stimulated with MDP (10μg/ml) for the time periods indicated. Cells were lysed, and an equal amount of total protein was immunoprecipitated (IP) with anti-Rip2 antibody (Santa Cruz Biotechnology) followed by immunoblotting (IB) with an anti-ubiquitin (anti Ub) antibody (Santa Cruz Biotechnology). Total immunoprecipitated Rip2 protein was measured by immunoblotting with anti-Rip2 antibody (Santa Cruz Biotechnology). Expression of Ubc13 level was determined by immunoblotting with an anti-Ubc13 antibody (Zymed Laboratories Inc.). B, Rip2 polyubiquitination requires the expression of the E3 ubiquitin ligase Traf6 but not Traf2. Omni-tagged NOD2 was expressed in HEK293T cells in the presence of either a control siRNA or siRNA specific for Traf2 or Traf6. Rip2 was immunoprecipitated with anti-Rip2 antibody (Santa Cruz Biotechnology) followed by immunoblotting with anti-ubiquitin to detect polyubiquitinated Rip2 proteins. Expression levels of Omni-NOD2 and Traf2 or Traf6 protein levels was measured by immunoblotting the total cell lysates with anti-Omni, anti-Traf6, and anti-Traf2 antibodies (Santa Cruz Biotechnology). C, MDP stimulates interaction between endogenous Rip2 and Traf6. RAW 264.7 macrophages were left untreated or treated with 10 μg/ml MDP for the indicated periods of time. Cells were lysed, and an equal amount of total protein was immunoprecipitated with anti-Rip2 antibody (Santa Cruz Biotechnology) followed by immunoblotting with an anti-Traf6 antibody (Santa Cruz Biotechnology). The total immunoprecipitated Rip2 protein was measured by immunoblotting with anti-Rip2 antibody (Santa Cruz Biotechnology). D, Traf6 expression is required for MDP- and IL-1-induced NF-κB activation. The RAW 264.7 macrophage cell line was transfected with control siRNA or a pool of Traf6 siRNAs. Forty eight hours later, the cells were left untreated or stimulated with MDP (10μg/ml) for the time periods indicated or with IL-α (5 ng/ml) for 10 min. NF-κB activation was measured by immunoblotting with a phospho-IκBα antibody (Cell Signaling Technology). Traf6 and β-actin levels were determined by immunoblotting with the indicated antibodies.View Large Image Figure ViewerDownload Hi-res image Download (PPT)In transfected cells, Rip2 has been shown to interact with Traf2, -5, and -6 proteins (6McCarthy J.V. Ni J. Dixit V.M. J. Biol. Chem. 1998; 273: 16968-16975Abstract Full Text Full Text PDF PubMed Scopus (361) Google Scholar), suggesting that one of these Traf proteins may modify Rip2 upon Nod2 pathway stimulation. To identify the E3 ubiquitin ligase responsible for the modification of Rip2, we transfected HEK293 cells with epitope-tagged versions of NOD2 and Rip2 and tested whether MDP- or NOD2-dependent Rip2 polyubiquitination is observed in cells where Traf2 or Traf6 expression was reduced. In HEK293 cells transfected with NOD2 and stimulated with MDP, Rip2 polyubiquitination was detected, as expected (Fig. 3B). Similarly, in cells where Traf2 expression is reduced via transfection of siRNAs specific for Traf2, MDP stimulated Rip2 polyubiquitination, and this modification appeared NOD2-dependent. In contrast, Rip2 polyubiquitination was reduced in MDP-stimulated HEK293 cells in which Traf6 expression was reduced (Fig. 3B), thereby implicating Traf6 as a potential Rip2 E3 ubiquitin ligase in the Nod2 pathway. We also examined whether MDP or NOD2 pathway activation stimulates an association between Rip2 and Traf6. Using co-immunoprecipitation, MDP treatment stimulated interaction between endogenous Rip2 and Traf6 between 30 and 60 min following MDP treatment. Consistently, polyubiquitinated Rip2 proteins are detected at similar time periods following MDP treatment (Fig. 2A).To further test a requirement for Traf6, we attempted to knock down the expression of Traf6 in the RAW 264.7 mouse macrophage cell line and then stimulated the cells with IL-1 or MDP. As expected, no IL-1-induced NF-κB activation is detected in the Traf6 knocked down cells; however, the control shRNA-treated cells activate NF-κB upon IL-1 treatment. MDP-induced NF-κB activation is clearly impaired in cells where Traf6 expression is reduced, suggesting that Traf6 is required for optimal NF-κB responses to MDP (Fig. 3D). These data are consistent with a model whereby Traf6 modifies Rip2 upon activation of the Nod2 pathway, raising the possibility that this enzyme may be targeted in human inflammatory disease.Our data suggest that Rip2 polyubiquitination may contribute to NOD2-mediated NF-κB activation by recruiting the ubiquitin-activated kinase Tak1. Therefore, we tested whether Rip2 interacts with Tak1 and whether MDP stimulates an endogenous Rip2/Tak1 interaction. A Rip2/Tak1 interaction could be readily demonstrated in transfected cells (Fig. 4A) and an endogenous Rip2/Tak1 interaction was detected following MDP treatment (Fig. 4B), during a time period when a Rip2/Traf6 interaction was also observed (Fig. 3C). Collectively, these data suggest that MDP stimulation or NOD2 pathway activation stimulates the formation of a Rip2-Ubc13-Traf6-Tak1 complex that results in the stable ubiquitin modification of Rip2.FIGURE 4Rip2 and the ubiquitin-activated kinase Tak1 interact upon MDP stimulation, and Tak1 expression is required for MDP-induced IKK activation. A, Rip2 and Tak1 interact in transfected cells. FLAG-tagged Tak1 and HA-tagged Rip2 were either co-expressed or expressed alone in HEK293T cells. Tak1 was immunoprecipitated (IP) with an anti-FLAG antibody and Rip2 detected by immunoblotting (IB) with anti-HA antibody, or Rip2 was immunoprecipitated with an anti-HA antibody followed by immunoblotting with anti-FLAG antibody to detect associated Tak1 proteins. Relative expression of each construct was measured by immunoblotting the total cell lysate with anti-HA or -FLAG antibodies. B, MDP stimulates interaction between Rip2 and Tak1. The RAW 264.7 macrophage cell line was left untreated or treated with 10 μg/ml MDP for the indicated periods of time. Cells were lysed, and an equal amount of total protein was immunoprecipitated with anti-Rip2 antibody (Santa Cruz Biotechnology) followed by immunoblotting with an anti-Tak1 antibody (Santa Cruz Biotechnology). Total immunoprecipitated Rip2 protein was measured by immunoblotting with anti-Rip2 antibody (Santa Cruz Biotechnology). C, Tak1 expression is required for TNF- and MDP-induced NF-κB activation. Mouse RAW 264.7 macrophages cell line was transfected with control siRNA or a pool of Tak1 siRNAs. Forty eight hours later, the cells were left untreated or stimulated with MDP (10 μg/ml) for the time periods indicated or with TNF-α (10 ng/ml) for 10 min. NF-κB activation was measured by immunoblotting with a phospho-IκBα antibody (Cell Signaling). Tak1 and β-actin levels were determined by immunoblotting with the indicated antibodies.View Large Image Figure ViewerDownload Hi-res image Download (PPT)These data predict that MDP-induced NF-κB activation will be dependent on the expression of the ubiquitin-dependent kinase Tak1. We reduced Tak1 expression levels in the RAW 264.7 macrophage cell line and tested its effects on MDP- and TNF-induced NF-κB activation. Consistent with the transfection studies, NF-κB activation was reduced in both the MDP- and TNF-stimulated Tak1 "silenced" cells, although it remained unaffected when the control cells were stimulated with either MDP or TNF-α (Fig. 4C). These data led us to propose that Tak1 is critical for NOD2 signaling to NF-κB. Thus, stimulation of the NOD2 pathway results in the recruitment and subsequent ubiquitin modification of Rip2 by a Ubc13-Uev1a and Traf6 complex. Polyubiquitinated Rip2 then signals the recruitment and activation of the Tak1 kinase.Although MDP stimulates NOD2-mediated NF-κB activation and mutations in the CARD15 gene are associated with human inflammatory disease, MDP has not, as yet, been shown to bind to the NOD2 protein (15Girardin S.E. Boneca I.G. Viala J. Chamaillard M. Labigne A. Thomas G. Philpott D.J. Sansonetti P.J. J. Biol. Chem. 2003; 278: 8869-8872Abstract Full Text Full Text PDF PubMed Scopus (1886) Google Scholar). Hence, we were interested in testing whether infection with live bacteria stimulates the ubiquitin modification of Rip2. The cytosolic NOD2 pathway has been implicated in the cytokine response to M. tuberculosis infection in vitro, and recent studies reveal important, nonredundant roles for NOD2 and TLRs in vivo in the recognition of M. tuberculosis (10Ferwerda G. Girardin S.E. Kullberg B.J. Le Bourhis L. de Jong D.J. Langenberg D.M. van Crevel R. Adema G.J. Ottenhoff T.H. Van der Meer J.W. Netea M.G. Plos Pathog. 2005; 1: 279-285Crossref PubMed Scopus (285) Google Scholar, 17Fremond C.M. Yeremeev V. Nicolle D.M. Jacobs M. Quesniaux V.F. Ryffel B. J. Clin. Investig. 2004; 114: 1790-1799Crossref PubMed Scopus (246) Google Scholar). To test whether M. tuberculosis infection stimulates Rip2 polyubiquitination, we infected bone marrow-derived macrophages with a virulent strain of M. tuberculosis (H37Rv) or with a heat-killed bacteria and assayed for polyubiquitinated Rip2 proteins at 1 and 4 h post-infection. Infection with live M. tuberculosis stimulated Rip2 polyubiquitination, whereas heat killing destroyed the ability of M. tuberculosis to induce the modification of Rip2 (Fig. 5A).FIGURE 5Live M. tuberculosis infection stimulates Rip2 polyubiquitination. A, live, virulent strains of M. tuberculosis (Rv) stimulate Rip2 polyubiquitination but heat-killed strains fail to stimulate Rip2 polyubiquitination. Wild type (WT) bone marrow-derived macrophages were infected with live virulent (Rv) or heat-killed (HK-Rv) strains of M. tuberculosis (M. tuberculosis H37Rv). Polyubiquitinated (Poly-Ub) Rip2 proteins were detected by immunoprec
Referência(s)