炎症体
脱氮酶
炎症
细胞生物学
白细胞介素18
泛素
肠粘膜
生物
免疫学
医学
癌症研究
化学
细胞因子
内科学
生物化学
基因
作者
Sandip Mukherjee,Ritesh Kumar,Elviche Tsakem Lenou,Venkatesha Basrur,Dimitris L. Kontoyiannis,Fotis Ioakeimidis,George Mosialos,Arianne L. Theiss,Richard A. Flavell,K. Venuprasad
标识
DOI:10.1038/s41590-020-0681-x
摘要
The inflammasome NLRP6 plays a crucial role in regulating inflammation and host defense against microorganisms in the intestine. However, the molecular mechanisms by which NLRP6 function is inhibited to prevent excessive inflammation remain unclear. Here, we demonstrate that the deubiquitinase Cyld prevents excessive interleukin 18 (IL-18) production in the colonic mucosa by deubiquitinating NLRP6. We show that deubiquitination inhibited the NLRP6-ASC inflammasome complex and regulated the maturation of IL-18. Cyld deficiency in mice resulted in elevated levels of active IL-18 and severe colonic inflammation following Citrobacter rodentium infection. Further, in patients with ulcerative colitis, the concentration of active IL-18 was inversely correlated with CYLD expression. Thus, we have identified a novel regulatory mechanism that inhibits the NLRP6-IL-18 pathway in intestinal inflammation.
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