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Reactive Oxygen Species Regulate Caspase-11 Expression and Activation of the Non-canonical NLRP3 Inflammasome during Enteric Pathogen Infection
Caspase-11 is required for NLRP3 inflammasome activation and cell death in response to certain gram-negative bacterial infections like Citrobacter rodentium. However, how C. rodentium drives caspase-11 expression and activation is not well understood. Here, we demonstrate that the NOD2-RIP2 pathway regulates reactive oxygen species production and c-Jun N-terminal kinase signaling to control caspase-11 expression and subsequent activation of caspase-11 and the NLRP3 inflammasome during C. rodentium infection. In the absence of NOD2-RIP2 signaling, increased inflammasome activation results in lower bacteria numbers in the colon and less tissue damage during the early stages of infection.
Vyšlo v časopise: Reactive Oxygen Species Regulate Caspase-11 Expression and Activation of the Non-canonical NLRP3 Inflammasome during Enteric Pathogen Infection. PLoS Pathog 10(9): e32767. doi:10.1371/journal.ppat.1004410
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1004410Souhrn
Caspase-11 is required for NLRP3 inflammasome activation and cell death in response to certain gram-negative bacterial infections like Citrobacter rodentium. However, how C. rodentium drives caspase-11 expression and activation is not well understood. Here, we demonstrate that the NOD2-RIP2 pathway regulates reactive oxygen species production and c-Jun N-terminal kinase signaling to control caspase-11 expression and subsequent activation of caspase-11 and the NLRP3 inflammasome during C. rodentium infection. In the absence of NOD2-RIP2 signaling, increased inflammasome activation results in lower bacteria numbers in the colon and less tissue damage during the early stages of infection.
Zdroje
1. KaperJB, NataroJP, MobleyHL (2004) Pathogenic Escherichia coli. Nat Rev Microbiol 2 : 123–140.
2. BorenshteinD, McBeeME, SchauerDB (2008) Utility of the Citrobacter rodentium infection model in laboratory mice. Curr Opin Gastroenterol 24 : 32–37.
3. MundyR, MacDonaldTT, DouganG, FrankelG, WilesS (2005) Citrobacter rodentium of mice and man. Cell Microbiol 7 : 1697–1706.
4. KamadaN, KimYG, ShamHP, VallanceBA, PuenteJL, et al. (2012) Regulated virulence controls the ability of a pathogen to compete with the gut microbiota. Science 336 : 1325–1329.
5. SimmonsCP, ClareS, Ghaem-MaghamiM, UrenTK, RankinJ, et al. (2003) Central role for B lymphocytes and CD4+ T cells in immunity to infection by the attaching and effacing pathogen Citrobacter rodentium. Infect Immun 71 : 5077–5086.
6. BryL, BrennerMB (2004) Critical role of T cell-dependent serum antibody, but not the gut-associated lymphoid tissue, for surviving acute mucosal infection with Citrobacter rodentium, an attaching and effacing pathogen. J Immunol 172 : 433–441.
7. GibsonDL, MaC, BergstromKS, HuangJT, ManC, et al. (2008) MyD88 signalling plays a critical role in host defence by controlling pathogen burden and promoting epithelial cell homeostasis during Citrobacter rodentium-induced colitis. Cell Microbiol 10 : 618–631.
8. GibsonDL, MaC, RosenbergerCM, BergstromKS, ValdezY, et al. (2008) Toll-like receptor 2 plays a critical role in maintaining mucosal integrity during Citrobacter rodentium-induced colitis. Cell Microbiol 10 : 388–403.
9. KimYG, KamadaN, ShawMH, WarnerN, ChenGY, et al. (2011) The Nod2 sensor promotes intestinal pathogen eradication via the chemokine CCL2-dependent recruitment of inflammatory monocytes. Immunity 34 : 769–780.
10. GeddesK, RubinoSJ, MagalhaesJG, StreutkerC, Le BourhisL, et al. (2011) Identification of an innate T helper type 17 response to intestinal bacterial pathogens. Nat Med 17 : 837–844.
11. GirardinSE, TournebizeR, MavrisM, PageAL, LiX, et al. (2001) CARD4/Nod1 mediates NF-kappaB and JNK activation by invasive Shigella flexneri. EMBO Rep 2 : 736–742.
12. BertinJ, NirWJ, FischerCM, TayberOV, ErradaPR, et al. (1999) Human CARD4 protein is a novel CED-4/Apaf-1 cell death family member that activates NF-kappaB. J Biol Chem 274 : 12955–12958.
13. ParkJH, KimYG, McDonaldC, KannegantiTD, HasegawaM, et al. (2007) RICK/RIP2 mediates innate immune responses induced through Nod1 and Nod2 but not TLRs. J Immunol 178 : 2380–2386.
14. Munoz-PlanilloR, KuffaP, Martinez-ColonG, SmithBL, RajendiranTM, et al. (2013) K(+) Efflux Is the Common Trigger of NLRP3 Inflammasome Activation by Bacterial Toxins and Particulate Matter. Immunity 38 : 1142–1153.
15. MeixenbergerK, PacheF, EitelJ, SchmeckB, HippenstielS, et al. (2010) Listeria monocytogenes-infected human peripheral blood mononuclear cells produce IL-1beta, depending on listeriolysin O and NLRP3. J Immunol 184 : 922–930.
16. WitzenrathM, PacheF, LorenzD, KoppeU, GutbierB, et al. (2011) The NLRP3 inflammasome is differentially activated by pneumolysin variants and contributes to host defense in pneumococcal pneumonia. J Immunol 187 : 434–440.
17. CassonCN, CopenhaverAM, ZwackEE, NguyenHT, StrowigT, et al. (2013) Caspase-11 activation in response to bacterial secretion systems that access the host cytosol. PLoS Pathog 9: e1003400.
18. BauernfeindFG, HorvathG, StutzA, AlnemriES, MacDonaldK, et al. (2009) Cutting edge: NF-kappaB activating pattern recognition and cytokine receptors license NLRP3 inflammasome activation by regulating NLRP3 expression. J Immunol 183 : 787–791.
19. LamkanfiM, KannegantiTD (2010) Nlrp3: an immune sensor of cellular stress and infection. Int J Biochem Cell Biol 42 : 792–795.
20. TschoppJ, SchroderK (2010) NLRP3 inflammasome activation: The convergence of multiple signalling pathways on ROS production? Nat Rev Immunol 10 : 210–215.
21. KannegantiTD, LamkanfiM, NunezG (2007) Intracellular NOD-like receptors in host defense and disease. Immunity 27 : 549–559.
22. KannegantiTD, OzorenN, Body-MalapelM, AmerA, ParkJH, et al. (2006) Bacterial RNA and small antiviral compounds activate caspase-1 through cryopyrin/Nalp3. Nature 440 : 233–236.
23. ManjiGA, WangL, GeddesBJ, BrownM, MerriamS, et al. (2002) PYPAF1, a PYRIN-containing Apaf1-like protein that assembles with ASC and regulates activation of NF-kappa B. J Biol Chem 277 : 11570–11575.
24. FinkSL, CooksonBT (2005) Apoptosis, pyroptosis, and necrosis: mechanistic description of dead and dying eukaryotic cells. Infect Immun 73 : 1907–1916.
25. MiaoEA, LeafIA, TreutingPM, MaoDP, DorsM, et al. (2010) Caspase-1-induced pyroptosis is an innate immune effector mechanism against intracellular bacteria. Nat Immunol 11 : 1136–1142.
26. KayagakiN, WarmingS, LamkanfiM, Vande WalleL, LouieS, et al. (2011) Non-canonical inflammasome activation targets caspase-11. Nature 479 : 117–121.
27. WangS, MiuraM, JungYK, ZhuH, LiE, et al. (1998) Murine caspase-11, an ICE-interacting protease, is essential for the activation of ICE. Cell 92 : 501–509.
28. CaseCL, KohlerLJ, LimaJB, StrowigT, de ZoeteMR, et al. (2013) Caspase-11 stimulates rapid flagellin-independent pyroptosis in response to Legionella pneumophila. Proc Natl Acad Sci U S A 110 : 1851–1856.
29. BrozP, RubyT, BelhocineK, BouleyDM, KayagakiN, et al. (2012) Caspase-11 increases susceptibility to Salmonella infection in the absence of caspase-1. Nature 490 : 288–291.
30. GurungP, MalireddiRK, AnandPK, DemonD, WalleLV, et al. (2012) Toll or interleukin-1 receptor (TIR) domain-containing adaptor inducing interferon-beta (TRIF)-mediated caspase-11 protease production integrates Toll-like receptor 4 (TLR4) protein - and Nlrp3 inflammasome-mediated host defense against enteropathogens. J Biol Chem 287 : 34474–34483.
31. RathinamVA, VanajaSK, WaggonerL, SokolovskaA, BeckerC, et al. (2012) TRIF licenses caspase-11-dependent NLRP3 inflammasome activation by gram-negative bacteria. Cell 150 : 606–619.
32. MariathasanS, NewtonK, MonackDM, VucicD, FrenchDM, et al. (2004) Differential activation of the inflammasome by caspase-1 adaptors ASC and Ipaf. Nature 430 : 213–218.
33. MartinonF, BurnsK, TschoppJ (2002) The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta. Mol Cell 10 : 417–426.
34. FranchiL, AmerA, Body-MalapelM, KannegantiTD, OzorenN, et al. (2006) Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1beta in salmonella-infected macrophages. Nat Immunol 7 : 576–582.
35. MiaoEA, Alpuche-ArandaCM, DorsM, ClarkAE, BaderMW, et al. (2006) Cytoplasmic flagellin activates caspase-1 and secretion of interleukin 1beta via Ipaf. Nat Immunol 7 : 569–575.
36. LamkanfiM, MuellerJL, VitariAC, MisaghiS, FedorovaA, et al. (2009) Glyburide inhibits the Cryopyrin/Nalp3 inflammasome. J Cell Biol 187 : 61–70.
37. NakahiraK, HaspelJA, RathinamVA, LeeSJ, DolinayT, et al. (2011) Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome. Nat Immunol 12 : 222–230.
38. ZhouR, YazdiAS, MenuP, TschoppJ (2011) A role for mitochondria in NLRP3 inflammasome activation. Nature 469 : 221–225.
39. LupferC, ThomasPG, AnandPK, VogelP, MilastaS, et al. (2013) Receptor interacting protein kinase 2-mediated mitophagy regulates inflammasome activation during virus infection. Nat Immunol 14 : 480–488.
40. KabeyaY, MizushimaN, UenoT, YamamotoA, KirisakoT, et al. (2000) LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing. EMBO J 19 : 5720–5728.
41. LoYY, WongJM, CruzTF (1996) Reactive oxygen species mediate cytokine activation of c-Jun NH2-terminal kinases. J Biol Chem 271 : 15703–15707.
42. YangS, WangB, HumphriesF, JacksonR, HealyME, et al. (2013) Pellino3 ubiquitinates RIP2 and mediates Nod2-induced signaling and protective effects in colitis. Nat Immunol 14 : 927–936.
43. MeunierE, DickMS, DreierRF, SchurmannN, Kenzelmann BrozD, et al. (2014) Caspase-11 activation requires lysis of pathogen-containing vacuoles by IFN-induced GTPases. Nature 509 : 366–370.
44. AachouiY, LeafIA, HagarJA, FontanaMF, CamposCG, et al. (2013) Caspase-11 protects against bacteria that escape the vacuole. Science 339 : 975–978.
45. PillaDM, HagarJA, HaldarAK, MasonAK, DegrandiD, et al. (2014) Guanylate binding proteins promote caspase-11-dependent pyroptosis in response to cytoplasmic LPS. Proc Natl Acad Sci U S A 111 : 6046–6051.
46. KayagakiN, WongMT, StoweIB, RamaniSR, GonzalezLC, et al. (2013) Noncanonical inflammasome activation by intracellular LPS independent of TLR4. Science 341 : 1246–1249.
47. HagarJA, PowellDA, AachouiY, ErnstRK, MiaoEA (2013) Cytoplasmic LPS activates caspase-11: implications in TLR4-independent endotoxic shock. Science 341 : 1250–1253.
48. LiuZ, ZakiMH, VogelP, GurungP, FinlayBB, et al. (2012) Role of inflammasomes in host defense against Citrobacter rodentium infection. J Biol Chem 287 : 16955–16964.
49. AkhterA, CautionK, Abu KhweekA, TaziM, AbdulrahmanBA, et al. (2012) Caspase-11 promotes the fusion of phagosomes harboring pathogenic bacteria with lysosomes by modulating actin polymerization. Immunity 37 : 35–47.
50. MonackDM, HershD, GhoriN, BouleyD, ZychlinskyA, et al. (2000) Salmonella exploits caspase-1 to colonize Peyer's patches in a murine typhoid model. J Exp Med 192 : 249–258.
51. KovarovaM, HeskerPR, JaniaL, NguyenM, SnouwaertJN, et al. (2012) NLRP1-dependent pyroptosis leads to acute lung injury and morbidity in mice. J Immunol 189 : 2006–2016.
52. WillinghamSB, AllenIC, BergstralhDT, BrickeyWJ, HuangMT, et al. (2009) NLRP3 (NALP3, Cryopyrin) facilitates in vivo caspase-1 activation, necrosis, and HMGB1 release via inflammasome-dependent and -independent pathways. J Immunol 183 : 2008–2015.
53. AnandPK, TaitSW, LamkanfiM, AmerAO, NunezG, et al. (2011) TLR2 and RIP2 pathways mediate autophagy of Listeria monocytogenes via extracellular signal-regulated kinase (ERK) activation. J Biol Chem 286 : 42981–42991.
54. BertrandMJ, DoironK, LabbeK, KornelukRG, BarkerPA, et al. (2009) Cellular inhibitors of apoptosis cIAP1 and cIAP2 are required for innate immunity signaling by the pattern recognition receptors NOD1 and NOD2. Immunity 30 : 789–801.
55. MariathasanS, WeissDS, NewtonK, McBrideJ, O'RourkeK, et al. (2006) Cryopyrin activates the inflammasome in response to toxins and ATP. Nature 440 : 228–232.
56. Said-SadierN, PadillaE, LangsleyG, OjciusDM (2010) Aspergillus fumigatus stimulates the NLRP3 inflammasome through a pathway requiring ROS production and the Syk tyrosine kinase. PLoS One 5: e10008.
57. HugotJP, ChamaillardM, ZoualiH, LesageS, CezardJP, et al. (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411 : 599–603.
58. ReingoldL, RahalK, Schmiedlin-RenP, RittershausAC, BenderD, et al. (2013) Development of a peptidoglycan-polysaccharide murine model of Crohn's disease: effect of genetic background. Inflamm Bowel Dis 19 : 1238–1244.
59. JamonttJ, PetitS, ClarkN, ParkinsonSJ, SmithP (2013) Nucleotide-binding oligomerization domain 2 signaling promotes hyperresponsive macrophages and colitis in IL-10-deficient mice. J Immunol 190 : 2948–2958.
60. Couturier-MaillardA, SecherT, RehmanA, NormandS, De ArcangelisA, et al. (2013) NOD2-mediated dysbiosis predisposes mice to transmissible colitis and colorectal cancer. J Clin Invest 123 : 700–711.
61. WatanabeT, KitaniA, MurrayPJ, WakatsukiY, FussIJ, et al. (2006) Nucleotide binding oligomerization domain 2 deficiency leads to dysregulated TLR2 signaling and induction of antigen-specific colitis. Immunity 25 : 473–485.
62. AmendolaA, ButeraA, SanchezM, StroberW, BoirivantM (2013) Nod2 deficiency is associated with an increased mucosal immunoregulatory response to commensal microorganisms. Mucosal Immunol 7 : 391–404.
63. KobayashiK, InoharaN, HernandezLD, GalanJE, NunezG, et al. (2002) RICK/Rip2/CARDIAK mediates signalling for receptors of the innate and adaptive immune systems. Nature 416 : 194–199.
64. KobayashiKS, ChamaillardM, OguraY, HenegariuO, InoharaN, et al. (2005) Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract. Science 307 : 731–734.
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