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Accueil Tous les numéros Volume 29 / Numéro 12 (Décembre 2013) Med Sci (Paris), 29 12 (2013) 1145-1150 Références
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Numéro
Med Sci (Paris)
Volume 29, Numéro 12, Décembre 2013
Page(s) 1145 - 1150
Section M/S Revues
DOI https://doi.org/10.1051/medsci/20132912019
Publié en ligne 20 décembre 2013
  1. MacDonald TT, Monteleone I, Fantini MC, Monteleone G. Regulation of homeostasis and inflammation in the intestine. Gastroenterology 2011 ; 140 : 1768–1775. [CrossRef] [PubMed] [Google Scholar]
  2. McGuckin MA, Eri R, Simms LA, et al. Intestinal barrier dysfunction in inflammatory bowel diseases. Inflamm Bowel Dis 2009 ; 15 : 100–113. [CrossRef] [PubMed] [Google Scholar]
  3. Maloy KJ, Powrie F. Intestinal homeostasis and its breakdown in inflammatory bowel disease. Nature 2011 ; 474 : 298–306. [CrossRef] [PubMed] [Google Scholar]
  4. Bevins CL, Salzman NH. Panethcells, antimicrobial peptides and maintenance of intestinal homeostasis. Nat Rev Microbiol 2011 ; 9 : 356–368. [CrossRef] [PubMed] [Google Scholar]
  5. Ramasundara M, Leach ST, Lemberg DA, Day AS. Defensins and inflammation: the role of defensins in inflammatory bowel disease. J Gastroenterol Hepatol 2009 ; 24 : 202–208. [CrossRef] [PubMed] [Google Scholar]
  6. Ganz T. Defensins: antimicrobial peptides of innate immunity. Nat Rev Immunol 2003 ; 3 : 710–720. [CrossRef] [PubMed] [Google Scholar]
  7. Roda G, Sartini A, Zambon E, et al. Intestinal epithelial cells in inflammatory bowel diseases. World J Gastroenterol 2010 ; 16 : 4264–4271. [CrossRef] [PubMed] [Google Scholar]
  8. Goto Y, Ivanov I. Intestinal epithelial cells as mediators of the commensal-host immune crosstalk. Immunol Cell Biol 2013 ; 91 : 204–214. [CrossRef] [PubMed] [Google Scholar]
  9. Laukoetter MG, Bruewer M, Nusrat A. Regulation of the intestinal epithelial barrier by the apical junctional complex. Curr Opin Gastroenterol 2006 ; 22 : 85–89. [CrossRef] [PubMed] [Google Scholar]
  10. Assimakopoulos SF, Papageorgiou I, Charonis A. Enterocyte’s tight junctions: from molecules to diseases. World J Gastrointest Pathophysiol 2011 ; 15 : 123–137. [CrossRef] [Google Scholar]
  11. Sudha PS, Devaraj H, Devaraj N. Adherence of Shigella dysenteriae 1 to human colonic mucin. Curr Microbiol 2001 ; 42 : 381–387. [CrossRef] [PubMed] [Google Scholar]
  12. Vaishnava S, Behrendt CL, Ismail AS, et al. Paneth cells directly sense gut commensals and maintain homeostasis at the intestinal host-microbial interface. Proc Natl Acad Sci USA 2008 ; 105 : 20858–20863. [CrossRef] [Google Scholar]
  13. Slack E. Innate and adaptive immunity cooperate flexibly to maintain host-microbiota mutualism. Science 2009 ; 325 : 617–620. [CrossRef] [PubMed] [Google Scholar]
  14. Yeretssian G. Effector functions of NLRs in the intestine: innate sensing, cell death, and disease. Immunol Res 2012 ; 54 : 25–36. [CrossRef] [PubMed] [Google Scholar]
  15. Lee J, Mo JH, Shen C, et al. Toll-like receptor signaling in intestinal epithelial cells contributes to colonic homoeostasis. Curr Opin Gastroenterol 2007 ; 23 : 27–31. [CrossRef] [PubMed] [Google Scholar]
  16. Kaser A, Niederreiter L, Blumberg RS. Genetically determined epithelial dysfunction and its consequences for microflora host interactions. Cell Mol Life Sci 2011 ; 68 : 3643–3649. [CrossRef] [PubMed] [Google Scholar]
  17. Thjodleifsson B, Sigthorsson G, Cariglia N, et al. Subclinical intestinal inflammation: an inherited abnormality in Crohn’s disease relatives? Gastroenterology 2003 ; 124 : 1728–1737. [CrossRef] [PubMed] [Google Scholar]
  18. Breslin NP, Nash C, Hilsden RJ, et al. Intestinal permeability is increased in a proportion of spouses of patients with Crohn’s disease. Am J Gastroenterol 2001 ; 96 : 2934–2938. [CrossRef] [PubMed] [Google Scholar]
  19. Utech M, Mennigen R, Bruewer M., Endocytosis and recycling of tight junction proteins in inflammation. J Biomed Biotechnol 2010 ; 2010 : 484987. [CrossRef] [PubMed] [Google Scholar]
  20. Kosiewicz MM, Nast CC, Krishnan A, et al. Th1-type responses mediate spontaneous ileitis in a novel murine model of Crohn’s disease. J Clin Invest 2001 ; 107 :695–702. [CrossRef] [PubMed] [Google Scholar]
  21. Vermeire S, Rutgeerts P. Current status of genetics research in inflammatory bowel disease. Genes Immun 2005 ; 6 : 637–645. [PubMed] [Google Scholar]
  22. Kanoh A, Takeuchi H, Kato K, et al. Interleukin-4 induces specific pp-GalNAc-T expression and alterations in mucin O-glycosylation in colonic epithelial cells. Biochim Biophys Acta 2008 ; 1780 :577–584. [CrossRef] [PubMed] [Google Scholar]
  23. Lu P, Burger-van Paassen N, Van der Sluis M, et al. Colonic gene expression patterns of mucin Muc2 knockout mice reveal various phases in colitis development. Inflamm Bowel Dis 2011 ; 17 : 2045–2057. [Google Scholar]
  24. Tytgat KMA, van der Wal JWG, Einerhand AWC, et al. Quantitative analysis of MUC2 synthesis in ulcerative colitis. Biochem Biophys Res Commun 1996 ; 224 : 397–405. [CrossRef] [PubMed] [Google Scholar]
  25. Mashimo H, Wu DC, Podolsky DK, Fishman MC. Impaired defense of intestinal mucosa in mice lacking intestinal trefoil factor. Science 1996 ; 274 : 262–265. [CrossRef] [PubMed] [Google Scholar]
  26. Tomasetto C, Masson R, Linares J, et al. pS2/TFF1 interacts directly with the VWFC cysteine-rich domains of mucins. Gastroenterology 2000 ; 118 : 70–80. [CrossRef] [PubMed] [Google Scholar]
  27. Zhao F, Edwards R, Dizon D, et al. Disruption of Paneth and goblet cell homeostasis and increased endoplasmic reticulum stress in Agr2-/- mice. Dev Biol 2010 ; 338 : 270–279. [CrossRef] [PubMed] [Google Scholar]
  28. Kaser A, Martinez-Naves E, Blumberg RS. Endoplasmic reticulum stress: implications for inflammatory bowel disease pathogenesis. Curr Opin Gastroenterol 2010 ; 26 : 318–326. [CrossRef] [PubMed] [Google Scholar]
  29. Tréton X, Pedruzzi E, Cazals-Hatem D, et al. Altered endoplasmic reticulum stress affects translation in inactive colon tissue from patients with ulcerative colitis. Gastroenterology 2011 ; 141 : 1024–1035. [CrossRef] [PubMed] [Google Scholar]
  30. Kaser A. XBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel disease. Cell 2008 ; 134 : 743–756. [CrossRef] [PubMed] [Google Scholar]
  31. Wehkamp J, Harder J, Weichenthal M, et al. NOD2 (CARD15) mutations in Crohn’s disease are associated with diminished mucosal alpha defensin expression. Gut 2004 ; 53 : 1653–1664. [CrossRef] [Google Scholar]
  32. Harris G, KuoLee R, Chen W. Role of Toll-like receptors in health and diseases of gastrointestinal tract. World J Gastroenterol 2006 ; 12 : 2149–2160. [PubMed] [Google Scholar]
  33. Cadwell, K. A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells. Nature 2008 ; 456 : 259–263. [CrossRef] [PubMed] [Google Scholar]
  34. Ayabe T, Satchell DP, Wilson CL, et al. Secretion of microbicidal alpha-defensins by intestinal Paneth cells in response to bacteria. Nat Immunol 2000 ; 1 : 113–118. [CrossRef] [PubMed] [Google Scholar]
  35. Arnott ID, Ho GT, Nimmo ER, Satsangi J., Toll-like receptor 4 gene in IBD: further evidence for genetic heterogeneity in Europe. Gut 2005 ; 54 : 308. [PubMed] [Google Scholar]
  36. Hiemstra IH, Bouma G, Geerts D, et al. Nod2 improves barrier function of intestinal epithelial cells via enhancement of TLR responses. Mol Immunol 2012 ; 52 : 264–272. [CrossRef] [PubMed] [Google Scholar]
  37. Jamilloux Y, Henry T. Les inflammasomes : plates-formes de l’immunité innée. Med Sci (Paris) 2013 ; 29 : 975–984. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  38. Matricon J. Immunopathogenèse des maladies inflammatoires chroniques de l’intestin. Med Sci (Paris) 2010 ; 26 : 405–410. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  39. Normand S, Secher T, Chamaillard M. La dysbiose, une nouvelle entité en médecine. Med Sci (Paris) 2013 ; 29 : 586–589. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  40. Rio MC. Fonctions paradoxales pour TFF1. Med Sci (Paris) 2002 ; 18 : 1177–1178. [CrossRef] [EDP Sciences] [Google Scholar]
  41. Zahraoui A. Les jonctions serrées : plate-forme de régulation de la prolifération et de la polarité cellulaire. Med Sci (Paris) 2004 ; 20 : 580–585. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]

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