细胞凋亡
信号转导
结肠炎
肠上皮
G蛋白偶联胆汁酸受体
蛋白激酶A
细胞生物学
化学
肠粘膜
激酶
药理学
生物
内分泌学
受体
内科学
免疫学
上皮
医学
生物化学
遗传学
作者
Wenji Yang,Fanghui Han,Yipei Gu,Hui Qu,Jia Liu,Jianhua Shen,Ying Leng
标识
DOI:10.1038/s41401-023-01081-y
摘要
Excessive apoptosis of intestinal epithelial cell (IEC) is a crucial cause of disrupted epithelium homeostasis, leading to the pathogenesis of ulcerative colitis (UC). The regulation of Takeda G protein-coupled receptor-5 (TGR5) in IEC apoptosis and the underlying molecular mechanisms remained unclear, and the direct evidence from selective TGR5 agonists for the treatment of UC is also lacking. Here, we synthesized a potent and selective TGR5 agonist OM8 with high distribution in intestinal tract and investigated its effect on IEC apoptosis and UC treatment. We showed that OM8 potently activated hTGR5 and mTGR5 with EC
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