生物
肝X受体
激素
胆固醇7α羟化酶
受体
胆固醇
内科学
低密度脂蛋白受体
平衡
胆固醇逆向转运
内分泌学
生物化学
核受体
脂蛋白
基因
转录因子
医学
作者
Xiaoli Hu,Fengyi Chen,Liangjie Jia,A. G. Long,Ying Peng,Xu Li,Junfeng Huang,Xueyun Wei,Xinlei Fang,Z Gao,Mengxian Zhang,Xiao Liu,Ye‐Guang Chen,Yan Wang,Huijie Zhang,Yiguo Wang
出处
期刊:Cell
[Elsevier]
日期:2024-03-01
卷期号:187 (7): 1685-1700.e18
被引量:13
标识
DOI:10.1016/j.cell.2024.02.024
摘要
The reciprocal coordination between cholesterol absorption in the intestine and de novo cholesterol synthesis in the liver is essential for maintaining cholesterol homeostasis, yet the mechanisms governing the opposing regulation of these processes remain poorly understood. Here, we identify a hormone, Cholesin, which is capable of inhibiting cholesterol synthesis in the liver, leading to a reduction in circulating cholesterol levels. Cholesin is encoded by a gene with a previously unknown function (C7orf50 in humans; 3110082I17Rik in mice). It is secreted from the intestine in response to cholesterol absorption and binds to GPR146, an orphan G-protein-coupled receptor, exerting antagonistic downstream effects by inhibiting PKA signaling and thereby suppressing SREBP2-controlled cholesterol synthesis in the liver. Therefore, our results demonstrate that the Cholesin-GPR146 axis mediates the inhibitory effect of intestinal cholesterol absorption on hepatic cholesterol synthesis. This discovered hormone, Cholesin, holds promise as an effective agent in combating hypercholesterolemia and atherosclerosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI