X-Box Binding Protein 1 (XBP1s) Is a Critical Determinant of Homoserine Lactone-Mediated Apoptosis
Pseudomonas aeruginosa infections are associated with high mortality rates and occur in diverse conditions including pneumonias, cystic fibrosis and neutropenia. Quorum sensing, mediated by small molecules including N-(3-oxo-dodecanoyl) homoserine lactone (C12), regulates P. aeruginosa growth and virulence. In addition, host cell recognition of C12 initiates multiple signalling responses including cell death. To gain insight into mechanisms of C12-mediated cytotoxicity, we studied the role of endoplasmic reticulum stress in host cell responses to C12. Dramatic protection against C12-mediated cell death was observed in cells that do not produce the X-box binding protein 1 transcription factor (XBP1s). The leucine zipper and transcriptional activation motifs of XBP1s were sufficient to restore C12-induced caspase activation in XBP1s-deficient cells, although this polypeptide was not transcriptionally active. The XBP1s polypeptide also regulated caspase activation in cells stimulated with N-(3-oxo-tetradecanoyl) homoserine lactone (C14), produced by Yersinia enterolitica and Burkholderia pseudomallei, and enhanced homoserine lactone-mediated caspase activation in the presence of endogenous XBP1s. In C12-tolerant cells, responses to C12 including phosphorylation of p38 MAPK and eukaryotic initiation factor 2α were conserved, suggesting that C12 cytotoxicity is not heavily dependent on these pathways. In summary, this study reveals a novel and unconventional role for XBP1s in regulating host cell cytotoxic responses to bacterial acyl homoserine lactones.
Vyšlo v časopise:
X-Box Binding Protein 1 (XBP1s) Is a Critical Determinant of Homoserine Lactone-Mediated Apoptosis. PLoS Pathog 9(8): e32767. doi:10.1371/journal.ppat.1003576
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1003576
Souhrn
Pseudomonas aeruginosa infections are associated with high mortality rates and occur in diverse conditions including pneumonias, cystic fibrosis and neutropenia. Quorum sensing, mediated by small molecules including N-(3-oxo-dodecanoyl) homoserine lactone (C12), regulates P. aeruginosa growth and virulence. In addition, host cell recognition of C12 initiates multiple signalling responses including cell death. To gain insight into mechanisms of C12-mediated cytotoxicity, we studied the role of endoplasmic reticulum stress in host cell responses to C12. Dramatic protection against C12-mediated cell death was observed in cells that do not produce the X-box binding protein 1 transcription factor (XBP1s). The leucine zipper and transcriptional activation motifs of XBP1s were sufficient to restore C12-induced caspase activation in XBP1s-deficient cells, although this polypeptide was not transcriptionally active. The XBP1s polypeptide also regulated caspase activation in cells stimulated with N-(3-oxo-tetradecanoyl) homoserine lactone (C14), produced by Yersinia enterolitica and Burkholderia pseudomallei, and enhanced homoserine lactone-mediated caspase activation in the presence of endogenous XBP1s. In C12-tolerant cells, responses to C12 including phosphorylation of p38 MAPK and eukaryotic initiation factor 2α were conserved, suggesting that C12 cytotoxicity is not heavily dependent on these pathways. In summary, this study reveals a novel and unconventional role for XBP1s in regulating host cell cytotoxic responses to bacterial acyl homoserine lactones.
Zdroje
1. GaynesR, EdwardsJR (2005) National Nosocomial Infections Surveillance System (2005) Overview of Nosocomial infections caused by Gram-negative Bacilli. Clin Infect Dis 15: 389–391.
2. CravenDE (2006) What is healthcare-associated pneumonia, and how should it be treated? Curr Opin Infect Dis 19: 153–160.
3. JonesRN (2010) Microbial etiologies of hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia. Clin Infect Dis 51: S81–S87.
4. FujitaniS, SunH-Y, YuVL, WeingartenJA (2011) Pneumonia due to Pseudomonas aeruginosa, Part I. Chest 139: 909–919.
5. MurrayTS, EganM, KazmierczakBI (2007) Pseudomonas aeruginosa chronic colonization in cystic fibrosis patients. Curr Opin Pediatr 19: 83–88.
6. BiltonD (2008) Update on non-cystic fibrosis bronchiectasis. Curr Opin Pulm Med 14: 595–599.
7. HuangYJ, KimE, CoxMJ, BrodieEL, BrownR, et al. (2010) A persistent and diverse microbiota present during chronic obstructive pulmonary disease exacerbations. OMICS 14: 9–59.
8. GiamarellouH, KanellakopoulouK (2008) Current therapies for Pseudomonas aeruginosa. Crit Care Clin 24: 261–278.
9. FlemmingHC, WingenderJ (2010) The biofilm matrix. Nat Rev Microbiol 8: 623–633.
10. HoJ, TambyahPA, PatersonDL (2010) Multiresistant Gram-negative infections: a global perspective. Curr Opin Infect Dis 23: 546–553.
11. PageMGP, HeimJ (2009) Prospects for the next anti-Pseudomonas drug. Curr Opin Pharm 9: 558–565.
12. LazdunskiA, VentreI, SturgisJN (2004) Regulatory circuits and communication in gram-negative bacteria. Nat Rev Immunol 2: 581–592.
13. CamilliA, BasslerBL (2006) Bacterial small-molecule signaling pathways. Science 311: 1113–1116.
14. RumbaughKP, KaufmannGF (2012) Exploitation of host signalling pathways by microbial quorum sensing signals. Curr Opin Microbiol 15: 162–168.
15. LiL, HooiD, ChhabraSR, PritchardD, ShawPE (2004) Bacterial N-acylhomoserine lactone-induced apoptosis in breast carcinoma cells correlated with down-modulation of STAT3. Oncogene 23: 4894–4902.
16. TatedaK, IshiiY, HorikawaM, MatsumotoT, MiyaririS, et al. (2003) The Pseudomonas aeruginosa autoinducer N-3-oxododecanoyl homoserine lactone accelerates apoptosis in macrophages and neutrophils. Infect Immun 71: 5785–5793.
17. KravchenkoVV, KaufmannGF, MathisonJC, ScottDA, KatzAZ, et al. (2006) N-(3-Oxo-acyl)homoserine lactones signal cell activation through a mechanism distinct from canonical pathogen-associated molecular pattern recognition receptor pathways. J Biol Chem 281: 28822–28830.
18. SchwarzerC, FuZ, PatanwalaM, HumL, Lopez-GuzmanM, et al. (2012) Pseudomonas aeruginosa biofilm-associated homoserine lactone C12 rapidly activates apoptosis in airway epithelia. Cell Microbiol 14: 698–709.
19. TelfordG, WheelerD, WilliamsP, TomkinsPT, ApplebyP, et al. (1998) The Pseudomonas aeruginosa quorum-sensing signal molecule N-(3-oxododecanoyl)-l-homoserine lactone has immunomodulatory activity. Infect Immun 66: 36–42.
20. RitchieAJ, JanssonA, StallbergJ, NilssonP, LysaghtP, et al. (2005) The Pseudomonas aeruginosa quorum-sensing molecule N-3-(oxododecanoyl)-l-homoserine lactone inhibits T-cell differentiation and cytokine production by a mechanism involving an early step in T-cell activation. Infect Immun 73: 1648–1655.
21. KravchenkoVV, KaufmannGF, MathisonJC, ScottDA, KatzAZ, et al. (2008) Modulation of gene expression via disruption of NF-κB signaling by bacterial small molecules. Science 321: 259–263.
22. SmithRS, KellyR, IglewskiBH, PhippsRP (2002) The Pseudomonas autoinducer N-(3-oxododecanoyl) homoserine lactone induced cyclooxygenase-2 and prostaglandin E2 production in human lung fibroblasts: implications for inflammation. J Immunol 169: 2636–2642.
23. MayerML, SheridanJA, BolohmkeCJ, TurveySE, HancockRE (2011) The Pseudomonas aeruginosa autoinducer 3O-C12 homoserine lactone provokes hyperinflammatory responses from cystic fibrosis airway epithelial cells. PLoS One 6: e16246.
24. ShinerEK, TerentyevD, BryanA, SennouneS, Martinez-ZaguilanR, et al. (2006) Pseudomonas aeruginosa autoinducer modulates host cell responses through calcium signalling. Cell Microbiol 8: 1601–1610.
25. SchwarzerC, WongS, ShiJ, MatthesE, IllekB, et al. (2010) Pseudomonas aeruginosa homoserine lactone activates store-operated cAMP and cystic fibrosis transmembrane regulator-dependent Cl− secretion by human airway epithelia. J Biol Chem 285: 34850–34863.
26. LeeRJ, XiongG, KofonowJM, ChenB, LysenkoA, et al. (2012) T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection. J Clin Invest 122: 4145–4159.
27. JahoorA, PatelR, BryanA, DoC, KrierJ, et al. (2008) Peroxisome proliferator-activated receptors mediate host cell proinflammatory responses to Pseudomonas aeruginosa autoinducer. J Bacteriol 190: 4408–4415.
28. DavisBM, JensenR, WilliamsP, O'SheaP (2010) The interaction of N-acylhomoserine lactone quorum sensing signalling molecules with biological membranes: Implications for inter-kingdom signalling. PLoS ONE 5: e13522.
29. TaitSWG, GreenDR (2010) Mitochondria and cell death: outer membrane permeabilization and beyond. Nat Rev Mol Cell Biol 11: 621–632.
30. TabasI, RonD (2011) Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress. Nat Cell Biol 13: 184–190.
31. SzegezdiE, LogueSE, GormanAM, SamaliA (2006) Mediators of endoplasmic reticulum stress-induced apoptosis. EMBO Rep 7: 880–885.
32. HardingHP, ZhangY, BertolottiA, ZengH, RonD (2000) Perk is essential for translational regulation and cell survival during the unfolded protein response. Mol Cell 5: 897–904.
33. HanD, LernerAG, Vande WalleL, UptonJ-P, XuW, et al. (2009) IRE1α kinase activation modes control alternative endoribonuclease outputs to determine divergent cell fates. Cell 138: 562–575.
34. CharltonTS, de NysR, NettingA, KumarN, HentzerM, et al. (2000) A novel and sensitive method for the quantification of N-3-oxoacyl homoserine lactones using gas chromatography-mass spectroscopy: application to a model of bacterial biofilm. Environ Microbiol 2: 530–541.
35. RonD, WalterP (2007) Signal integration in the endoplasmic reticulum unfolded protein response. Nat Rev Mol Cell Biol 8: 519–529.
36. YoshidaH, OkuM, SuzukiM, MoriK (2006) pXBP1(U) encoded in XBP1 pre-mRNA negatively regulates unfolded protein response activator pXBP1(S) in mammalian ER stress response. J Cell Biol 172: 565–575.
37. UranoF, WangX, BertolottiA, ZhangY, ChungP, et al. (2000) Coupling of stress in the ER to activation of JNK protein kinases by transmembrane protein kinase IRE1. Science 287: 664–666.
38. ShoreGC, PapaFR, OakesSA (2011) Signaling cell death from the endoplasmic reticulum stress response. Curr Opin Cell Biol 23: 143–149.
39. LernerAG, UptonJ-P, PraveenPVK, GhoshR, NakagawaY, et al. (2012) IRE1α induces thioredoxin-interacting protein to activate the NLRP3 inflammasome and promote programmed cell death under irremedial ER stress. Cell Metab 16: 250–264.
40. PapandreouI, DenkoNC, OlsonM, van MelckebekeH, LustS, et al. (2011) Identification of an Ire1α endonuclease specific inhibitor with cytotoxic activity against human multiple myeloma. Blood 117: 1311–1314.
41. SpiottoMT, BanhA, PapandreouI, CaoH, GalvezMG, et al. (2010) Imaging the unfolded protein response in primary tumors reveals microenvironments with metabolic variations that predict tumor growth. Cancer Res 70: 78–88.
42. LeeK, TirasophonW, ShenX, MichalakM, PrywesR, et al. (2002) IRE1-mediated unconventional mRNA splicing and SP2-mediated ATF6 cleavage merge to regulate XBP1 in signaling the unfolded protein response. Genes Dev 16: 452–466.
43. WangY, ShenJ, ArenzanaN, TirasophonW, KaufmanRJ, et al. (2000) Activation of ATF6 and an ATF6 DNA binding site by the endoplasmic reticulum stress response. J Biol Chem 275: 27013–27020.
44. LeeA-H, IwakowshiNN, GlimcherLH (2003) XBP-1 regulates a subset of endoplasmic reticulum resident chaperone genes in the unfolded response. Mol Cell Biol 23: 7448–7459.
45. SuAI, WiltshireT, BatalovS, LappH, ChingKA, et al. (2004) A gene atlas of the mouse and human protein-encoding transcriptomes. Proc Natl Acad Sci USA 101: 6062–6067.
46. SmithRS, HarrisSG, PhippsR, IglewskiBH (2002) The Pseudomonas aeruginosa quorum-sensing molecule N-(3-oxododecanoyl) homoserine lactone contributes to virulence and induces inflammation in vivo. J Bacteriol 184: 1132–1139.
47. SriramuluDD, LunsdorfH, LamJS, RomlingU (2005) Microcolony formation: a novel biofilm model of Pseudomonas aeruginosa for cystic fibrosis lung. J Med Microbiol 54: 667–676.
48. KravchenkoVV, KaufmannGF (2013) Bacterial inhibition of inflammatory responses via TLR-independent mechanisms. Cell Microbiol 15: 527–536.
49. Acosta-AlvearD, ZhouY-Y, BlaisA, TsikitisM, LentsNH, et al. (2007) XBP1 controls diverse cell type- and condition-specific transcriptional regulatory networks. Mol Cell 27: 53–66.
50. MasakiT, YoshidaM, NoguchiS (1999) Targeted disruption of CRE-binding factor TREB5 gene leads to cellular necrosis in cardiac myocytes at the embryonic stage. Biochem Biophys Res Commun 261: 350–356.
51. ReimoldAM, EtkinA, ClaussI, PerkinsA, FriendDS, et al. (2000) An essential role in liver development for the transcription factor XBP-1. Genes Dev 14: 152–157.
52. ReimoldAM, IwakoshiNN, ManisJ, VallabhajosyulaP, Szomolanyi-TsudaE, et al. (2001) Plasma cell differentiation requires the transcription factor XBP-1. Nature 412: 300–307.
53. LeeA-H, ChuGC, IwakoshiNN, GlimcherLH (2005) XBP-1 is required for biogenesis of cellular secretory machinery of exocrine glands. EMBO J 24: 4368–4380.
54. KaserA, LeeA-H, FrankeA, GlickmanJN, ZeissigS, et al. (2008) XBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel disease. Cell 134: 743–756.
55. RichardsonCE, KooistraT, KimDH (2010) An essential role for XBP-1 in host protection against immune activation in C. elegans. Nature 463: 1092–1095.
56. ZengL, ZampetakiA, MargaritiA, PepeAE, AlamS, et al. (2009) Sustained activation of XBP1 splicing leads to endothelial apoptosis and atherosclerosis development in response to disturbed flow. Proc Natl Acad Sci USA 106: 8326–8331.
57. AllagnatF, ChristuliaF, OrtisF, PirotP, LortzS, et al. (2010) Sustained production of spliced X-box binding protein 1 (XBP1) induces pancreatic β cell dysfunction and apoptosis. Diabetologia 53: 1120–1130.
58. MartinonF, ChenX, LeeA-H, GlimcherLH (2010) TLR activation of the transcription factor XBP1 regulates innate immune responses in macrophages. Nat Immunol 11: 411–418.
59. BertolottiA, ZhangY, HendershotLM, HardingHP, RonD (2000) Dynamic interactions of BiP and ER stress transducers in the unfolded-protein response. Nat Cell Biol 2: 326–332.
60. SamuelCE (1993) The eIF-2α protein kinases, regulators of translation in eukaryotes from yeast to humans. J Biol Chem 268: 7603–7606.
61. HebbarN, WangC, RangnekarVM (2012) Mechanisms of apoptosis by the tumor suppressor Par-4. J Cell Physiol 227: 3715–3721.
62. PominiAM, MarsaioliAJ (2008) Absolute configuration and antimicrobial activity of acylhomoserine lactones. J Nat Prod 71: 1032–1036.
63. CalfonM, ZengH, UranoF, TillJH, HubbardSR, et al. (2002) IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA. Nature 415: 92–96.
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2013 Číslo 8
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Host Immune Response to Intestinal Amebiasis
- Discovery of Anthelmintic Drug Targets and Drugs Using Chokepoints in Nematode Metabolic Pathways
- Bed Bugs and Infectious Disease: A Case for the Arboviruses
- Relevance of Trehalose in Pathogenicity: Some General Rules, Yet Many Exceptions