Dagenais Maryse, Douglas Todd, Saleh Maya
aDepartments of Biochemistry bMicrobiology and Immunology cMedicine, McGill University, Montréal, Québec, Canada.
Curr Opin Gastroenterol. 2014 Nov;30(6):566-75. doi: 10.1097/MOG.0000000000000117.
To critically review recent advances on the role of programmed necrosis and other cell death modalities in intestinal health and inflammatory bowel disease.
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.
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.
批判性地回顾程序性坏死及其他细胞死亡方式在肠道健康和炎症性肠病中的作用的最新进展。
肠道生理学需要严格调控肠道上皮细胞增殖和细胞死亡,以维持完整的屏障,限制微生物群易位并确保免疫耐受。长期以来,凋亡一直被认为是肠道上皮细胞更新的正常组成部分。然而,最近的研究表明,如在炎症性肠病中所观察到的,过度的细胞死亡会导致有害的肠道炎症。此外,一种被称为程序性坏死或坏死性凋亡的新型细胞死亡形式最近已被证明在肠道中具有病理学意义。
细胞死亡在肠道中的作用很复杂,其在肠道疾病尤其是炎症性肠病中的潜在影响需要重新评估。