Ubiquitin-specific proteases in inflammatory bowel disease-related signalling pathway regulation

被引:31
|
作者
Chen, Rirong [1 ]
Pang, Xiaobai [2 ]
Li, Li [1 ]
Zeng, Zhirong [1 ]
Chen, Minhu [1 ]
Zhang, Shenghong [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Gastroenterol, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; STEM-CELL DIFFERENTIATION; DEUBIQUITINATING ENZYME; SUSCEPTIBILITY LOCI; INTESTINAL HOMEOSTASIS; BARRIER FUNCTION; CROHNS-DISEASE; CYLD USP; ACTIVATION; POLYUBIQUITIN;
D O I
10.1038/s41419-022-04566-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The exact pathogenesis of inflammatory bowel disease (IBD), a chronic gastrointestinal inflammatory disease comprising Crohn's disease and ulcerative colitis, remains unclear. Studies on ubiquitination, which regulates the degradation of inflammation signalling pathway molecules, and deubiquitination have provided novel insights. Targeting the ubiquitin-specific protease (USP) family of deubiquitinases elucidates IBD signalling pathway mechanisms and possibly, IBD therapeutic solutions. Here, we characterised USPs as chief regulators of pro-inflammatory signalling pathways, including nuclear factor-kappa B and transforming growth factor-beta; analysed the relationship between USPs and IBD pathogenesis in terms of genetic susceptibility, intestinal epithelial barrier, immunity, and gut microbiota; and discussed future research prospects.
引用
收藏
页数:11
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