Heads up! How the intestinal epithelium safeguards mucosal barrier immunity through the inflammasome and beyond

被引:40
作者
Cario, Elke [1 ,2 ]
机构
[1] Univ Duisburg Essen, Univ Hosp Essen, Div Gastroenterol & Hepatol, Essen, Germany
[2] Univ Duisburg Essen, Sch Med, Essen, Germany
关键词
host defense; inflammasome; inflammatory bowel diseases; intestinal epithelial cell; mucosal barrier; NLRP3; NOD-like receptors; Toll-like receptors; TOLL-LIKE RECEPTOR-4; CROHNS-DISEASE SUSCEPTIBILITY; GENOME-WIDE ASSOCIATION; MURINE MODEL; IL-1-BETA-CONVERTING ENZYME; NLRP3; INFLAMMASOME; BOWEL-DISEASE; PANETH CELLS; COLITIS; AUTOPHAGY;
D O I
10.1097/MOG.0b013e32833d4b88
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review The intestinal epithelium serves as a highly dynamic immunologic frontier - exhibiting both innate and adaptive immune features. This review focuses on recent advances and novel insights into key intrinsic processes of the intestinal epithelium to closely monitor its intracellular and extracellular environment, communicate messages to neighbouring cells and rapidly initiate active defensive and repair measures, if necessary. Recent findings The intestinal epithelium is uniquely equipped with a vast array of features to control immune barrier homeostasis at the gates of the healthy intestinal mucosa. Deficient Toll-like receptor or NOD-like receptor signalling in the intestinal epithelium may imbalance commensal-dependent homeostasis, facilitating mucosal injury and leading to inflammatory disease. Dysfunction of the NLRP3 inflammasome may trigger aggravation of mucosal inflammation and cancer and has been associated with human inflammatory bowel diseases. Deregulated autophagy may alter inflammasome activity. Summary Exciting progress has been made in better understanding the complex diversity of physiological functions of innate immune responses in the intestinal epithelial barrier. Regulatory platforms of signalling mechanisms exist which are closely related and interact. However, many questions remain to be answered and more puzzles have arisen which are highlighted here.
引用
收藏
页码:583 / 590
页数:8
相关论文
共 61 条
[1]   Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function [J].
Adachi, O ;
Kawai, T ;
Takeda, K ;
Matsumoto, M ;
Tsutsui, H ;
Sakagami, M ;
Nakanishi, K ;
Akira, S .
IMMUNITY, 1998, 9 (01) :143-150
[2]   IL-1β causes an increase in intestinal epithelial tight junction permeability [J].
Al-Sadi, Rana M. ;
Ma, Thomas Y. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (07) :4641-4649
[3]   The NLRP3 inflammasome functions as a negative regulator of tumorigenesis during colitis-associated cancer [J].
Allen, Irving C. ;
TeKippe, Erin McElvania ;
Woodford, Rita-Marie T. ;
Uronis, Joshua M. ;
Holl, Eda K. ;
Rogers, Arlin B. ;
Herfarth, Hans H. ;
Jobin, Christian ;
Ting, Jenny P. -Y. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2010, 207 (05) :1045-1056
[4]   The bacterial signal indole increases epithelial-cell tight-junction resistance and attenuates indicators of inflammation [J].
Bansal, Tarun ;
Alaniz, Robert C. ;
Wood, Thomas K. ;
Jayaraman, Arul .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (01) :228-233
[5]   Exploring the interplay of barrier function and leukocyte recruitment in intestinal inflammation by targeting fucosyltransferase VII and trefoil factor 3 [J].
Beck, P. L. ;
Ihara, E. ;
Hirota, S. A. ;
MacDonald, J. A. ;
Meng, D. ;
Nanthakumar, N. N. ;
Podolsky, D. K. ;
Xavier, R. J. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2010, 299 (01) :G43-G53
[6]   Myd88-dependent positioning of Ptgs2-expressing stromal cells maintains colonic epithelial proliferation during injury [J].
Brown, Sarah L. ;
Riehl, Terrence E. ;
Walker, Monica R. ;
Geske, Michael J. ;
Doherty, Jason M. ;
Stenson, William F. ;
Stappenbeck, Thaddeus S. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (01) :258-269
[7]   Inflammasome-Mediated Disease Animal Models Reveal Roles for Innate but Not Adaptive Immunity [J].
Brydges, Susannah D. ;
Mueller, James L. ;
McGeough, Matthew D. ;
Pena, Carla A. ;
Misaghi, Amirhossein ;
Gandhi, Chhavi ;
Putnam, Chris D. ;
Boyle, David L. ;
Firestein, Gary S. ;
Horner, Anthony A. ;
Soroosh, Pejman ;
Watford, Wendy T. ;
O'Shea, John J. ;
Kastner, Daniel L. ;
Hoffman, Hal M. .
IMMUNITY, 2009, 30 (06) :875-887
[8]   Membrane-anchored serine protease matriptase regulates epithelial barrier formation and permeability in the intestine [J].
Buzza, Marguerite S. ;
Netzel-Arnett, Sarah ;
Shea-Donohue, Terez ;
Zhao, Aiping ;
Lin, Chen-Yong ;
List, Karin ;
Szabo, Roman ;
Fasano, Alessio ;
Bugge, Thomas H. ;
Antalis, Toni M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (09) :4200-4205
[9]   A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells [J].
Cadwell, Ken ;
Liu, John Y. ;
Brown, Sarah L. ;
Miyoshi, Hiroyuki ;
Loh, Joy ;
Lennerz, Jochen K. ;
Kishi, Chieko ;
Kc, Wumesh ;
Carrero, Javier A. ;
Hunt, Steven ;
Stone, Christian D. ;
Brunt, Elizabeth M. ;
Xavier, Ramnik J. ;
Sleckman, Barry P. ;
Li, Ellen ;
Mizushima, Noboru ;
Stappenbeck, Thaddeus S. ;
Virgin, Herbert W. .
NATURE, 2008, 456 (7219) :259-U62
[10]   Differential alteration in intestinal epithelial cell expression of Toll-like receptor 3 (TLR3) and TLR4 in inflammatory bowel disease [J].
Cario, E ;
Podolsky, DK .
INFECTION AND IMMUNITY, 2000, 68 (12) :7010-7017