泛素
炎症性肠病
脱氮酶
泛素连接酶
生物
免疫学
泛素类
泛素蛋白连接酶类
疾病
医学
细胞生物学
生物信息学
癌症研究
遗传学
病理
基因
作者
Min Zou,Qi‐Shan Zeng,Jiao Nie,Jiahui Yang,Zhen-Yi Luo,Huatian Gan
标识
DOI:10.3389/fimmu.2021.769167
摘要
Inflammatory bowel disease (IBD), which include Crohn’s disease (CD) and ulcerative colitis (UC), exhibits a complex multifactorial pathogenesis involving genetic susceptibility, imbalance of gut microbiota, mucosal immune disorder and environmental factors. Recent studies reported associations between ubiquitination and deubiquitination and the occurrence and development of inflammatory bowel disease. Ubiquitination modification, one of the most important types of post-translational modifications, is a multi-step enzymatic process involved in the regulation of various physiological processes of cells, including cell cycle progression, cell differentiation, apoptosis, and innate and adaptive immune responses. Alterations in ubiquitination and deubiquitination can lead to various diseases, including IBD. Here, we review the role of E3 ubiquitin ligases and deubiquitinases (DUBs) and their mediated ubiquitination and deubiquitination modifications in the pathogenesis of IBD. We highlight the importance of this type of posttranslational modification in the development of inflammation, and provide guidance for the future development of targeted therapeutics in IBD.
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