Epithelial IL-18 Equilibrium Controls Barrier Function in Colitis

被引:563
作者
Nowarski, Roni [1 ]
Jackson, Ruaidhri [1 ]
Gagliani, Nicola [1 ]
de Zoete, Marcel R. [1 ]
Palm, Noah W. [1 ]
Bailis, Will [1 ]
Low, Jun Siong [1 ]
Harman, Christian C. D. [1 ]
Graham, Morven [2 ]
Elinav, Eran [3 ]
Flavell, Richard A. [1 ,4 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Ctr Cellular & Mol Imaging, New Haven, CT 06520 USA
[3] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[4] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
INFLAMMATORY-BOWEL-DISEASE; TNF-ALPHA PRODUCTION; CROHNS-DISEASE; ULCERATIVE-COLITIS; INTESTINAL INFLAMMATION; BINDING-PROTEIN; MURINE COLITIS; GOBLET CELLS; CUTTING EDGE; PANETH CELLS;
D O I
10.1016/j.cell.2015.10.072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The intestinal mucosal barrier controlling the resident microbiome is dependent on a protective mucus layer generated by goblet cells, impairment of which is a hallmark of the inflammatory bowel disease, ulcerative colitis. Here, we show that IL-18 is critical in driving the pathologic breakdown of barrier integrity in a model of colitis. Deletion of Il18 or its receptor Il18r1 in intestinal epithelial cells (D/EC) conferred protection from colitis and mucosal damage in mice. In contrast, deletion of the IL-18 negative regulator Il18bp resulted in severe colitis associated with loss of mature goblet cells. Colitis and goblet cell loss were rescued in Il18bp(-/-);Il18r(Delta/EC) mice, demonstrating that colitis severity is controlled at the level of IL-18 signaling in intestinal epithelial cells. IL-18 inhibited goblet cell maturation by regulating the transcriptional program instructing goblet cell development. These results inform on the mechanism of goblet cell dysfunction that underlies the pathology of ulcerative colitis.
引用
收藏
页码:1444 / 1456
页数:13
相关论文
共 68 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]
Paneth cells as a site of origin for intestinal inflammation [J].
Adolph, Timon E. ;
Tomczak, Michal F. ;
Niederreiter, Lukas ;
Ko, Hyun-Jeong ;
Boeck, Janne ;
Martinez-Naves, Eduardo ;
Glickman, Jonathan N. ;
Tschurtschenthaler, Markus ;
Hartwig, John ;
Hosomi, Shuhei ;
Flak, Magdalena B. ;
Cusick, Jennifer L. ;
Kohno, Kenji ;
Iwawaki, Takao ;
Billmann-Born, Susanne ;
Raine, Tim ;
Bharti, Richa ;
Lucius, Ralph ;
Kweon, Mi-Na ;
Marciniak, Stefan J. ;
Choi, Augustine ;
Hagen, Susan J. ;
Schreiber, Stefan ;
Rosenstiel, Philip ;
Kaser, Arthur ;
Blumberg, Richard S. .
NATURE, 2013, 503 (7475) :272-+
[3]
An innately dangerous balancing act: intestinal homeostasis, inflammation, and colitis-associated cancer [J].
Asquith, Mark ;
Powrie, Fiona .
JOURNAL OF EXPERIMENTAL MEDICINE, 2010, 207 (08) :1573-1577
[4]
New insights into the dichotomous role of innate cytokines in gut homeostasis and inflammation [J].
Bamias, Giorgos ;
Corridoni, Daniele ;
Pizarro, Theresa T. ;
Cominelli, Fabio .
CYTOKINE, 2012, 59 (03) :451-459
[5]
Cutting Edge: NF-κB Activating Pattern Recognition and Cytokine Receptors License NLRP3 Inflammasome Activation by Regulating NLRP3 Expression [J].
Bauernfeind, Franz G. ;
Horvath, Gabor ;
Stutz, Andrea ;
Alnemri, Emad S. ;
MacDonald, Kelly ;
Speert, David ;
Fernandes-Alnemri, Teresa ;
Wu, Jianghong ;
Monks, Brian G. ;
Fitzgerald, Katherine A. ;
Hornung, Veit ;
Latz, Eicke .
JOURNAL OF IMMUNOLOGY, 2009, 183 (02) :787-791
[6]
High resolution colonoscopy in live mice [J].
Becker, C. ;
Fantini, M. C. ;
Neurath, M. F. .
NATURE PROTOCOLS, 2006, 1 (06) :2900-2904
[7]
Modulation of intestinal goblet cell function during infection by an attaching and effacing bacterial pathogen [J].
Bergstrom, Kirk S. B. ;
Guttman, Julian A. ;
Rumi, Mohammad ;
Ma, Caixia ;
Bouzari, Saied ;
Khan, Mohammed A. ;
Gibson, Deanna L. ;
Vogl, A. Wayne ;
Vallance, Bruce A. .
INFECTION AND IMMUNITY, 2008, 76 (02) :796-811
[8]
Non-redundant properties of IL-1α and IL-1β during acute colon inflammation in mice [J].
Bersudsky, Marina ;
Luski, Lotem ;
Fishman, Daniel ;
White, Rosalyn M. ;
Ziv-Sokolovskaya, Nadya ;
Dotan, Shahar ;
Rider, Peleg ;
Kaplanov, Irena ;
Aychek, Tegest ;
Dinarello, Charles A. ;
Apte, Ron N. ;
Voronov, Elena .
GUT, 2014, 63 (04) :598-609
[9]
Cloning of a novel receptor subunit, AcPL, required for interleukin-18 signaling [J].
Born, TL ;
Thomassen, E ;
Bird, TA ;
Sims, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (45) :29445-29450
[10]
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