Role of programmed necrosis and cell death in intestinal inflammation

被引:25
|
作者
Dagenais, Maryse [1 ]
Douglas, Todd [2 ]
Saleh, Maya [1 ,2 ,3 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ, Canada
[2] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[3] McGill Univ, Dept Med, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
apoptosis; caspase; inflammation; inflammatory bowel disease; necroptosis; MIXED LINEAGE KINASE; INNATE IMMUNE-SYSTEM; DOMAIN-LIKE PROTEIN; BOWEL-DISEASE; CROHNS-DISEASE; ULCERATIVE-COLITIS; EPITHELIAL-CELLS; IN-VIVO; BARRIER FUNCTION; C-FLIP;
D O I
10.1097/MOG.0000000000000117
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review To critically review recent advances on the role of programmed necrosis and other cell death modalities in intestinal health and inflammatory bowel disease. Recent findings Tight regulation of intestinal epithelial cell proliferation and cell death is required for intestinal physiology, and to maintain an integral barrier that restricts microbiota translocation and ensures immune tolerance. Apoptosis has long been considered as a normal part of intestinal epithelial cell turnover. However, recent studies have demonstrated that excessive cell death leads to deleterious intestinal inflammation, as is observed in inflammatory bowel disease. Additionally, a novel form of cell death dubbed programmed necrosis, or necroptosis, has been recently shown to be pathological in the gut. Summary The role of cell death in the intestine is complex and its potential implication in intestinal diseases, and inflammatory bowel disease in particular, needs to be reevaluated.
引用
收藏
页码:566 / 575
页数:10
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