STAT3 links IL-22 signaling in intestinal epithelial cells to mucosal wound healing.

Détails

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Etat: Public
Version: de l'auteur
ID Serval
serval:BIB_34B92923E041
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
STAT3 links IL-22 signaling in intestinal epithelial cells to mucosal wound healing.
Périodique
Journal of Experimental Medicine
Auteur(s)
Pickert G., Neufert C., Leppkes M., Zheng Y., Wittkopf N., Warntjen M., Lehr H.A., Hirth S., Weigmann B., Wirtz S., Ouyang W., Neurath M.F., Becker C.
ISSN
1540-9538[electronic]
Statut éditorial
Publié
Date de publication
2009
Peer-reviewed
Oui
Volume
206
Numéro
7
Pages
1465-1472
Langue
anglais
Notes
Publication types: Journal Article
Résumé
Signal transducer and activator of transcription (STAT) 3 is a pleiotropic transcription factor with important functions in cytokine signaling in a variety of tissues. However, the role of STAT3 in the intestinal epithelium is not well understood. We demonstrate that development of colonic inflammation is associated with the induction of STAT3 activity in intestinal epithelial cells (IECs). Studies in genetically engineered mice showed that epithelial STAT3 activation in dextran sodium sulfate colitis is dependent on interleukin (IL)-22 rather than IL-6. IL-22 was secreted by colonic CD11c(+) cells in response to Toll-like receptor stimulation. Conditional knockout mice with an IEC-specific deletion of STAT3 activity were highly susceptible to experimental colitis, indicating that epithelial STAT3 regulates gut homeostasis. STAT3(IEC-KO) mice, upon induction of colitis, showed a striking defect of epithelial restitution. Gene chip analysis indicated that STAT3 regulates the cellular stress response, apoptosis, and pathways associated with wound healing in IECs. Consistently, both IL-22 and epithelial STAT3 were found to be important in wound-healing experiments in vivo. In summary, our data suggest that intestinal epithelial STAT3 activation regulates immune homeostasis in the gut by promoting IL-22-dependent mucosal wound healing.
Mots-clé
Animals, Colitis/chemically induced, Colitis/immunology, Dextran Sulfate/pharmacology, Epithelial Cells/cytology, Epithelial Cells/physiology, Gene Expression Profiling, Inflammation/immunology, Inflammation/pathology, Interleukin-6/genetics, Interleukin-6/immunology, Interleukins/genetics, Interleukins/immunology, Intestinal Mucosa/cytology, Intestinal Mucosa/pathology, Mice, Mice, Inbred C57BL, Mice, Knockout, Oligonucleotide Array Sequence Analysis, STAT3 Transcription Factor/genetics, STAT3 Transcription Factor/metabolism, Signal Transduction/physiology, Wound Healing
Pubmed
Web of science
Open Access
Oui
Création de la notice
20/07/2009 9:49
Dernière modification de la notice
20/08/2019 14:21
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