受体
血管紧张素II
背景(考古学)
肾素-血管紧张素系统
内化
逮捕
G蛋白偶联受体
信号转导
生物
血管紧张素受体
细胞生物学
药理学
内分泌学
生物化学
血压
古生物学
作者
Caroline Antunes Lino,Maria Luiza Morais Barreto‐Chaves
标识
DOI:10.1016/j.cellsig.2022.110253
摘要
Cardiovascular diseases are the leading cause of death worldwide. The renin-angiotensin-aldosterone system is one of the major regulators of cardiovascular homeostasis and the angiotensin II type 1 receptor (AT1R) mediates the main deleterious effects resulting from the hyperactivation of this hormonal system. Beta-arrestins are multifunctional proteins that regulate the desensitization and internalization of G protein-coupled receptors. After the discovery of beta-arrestins, many efforts have been made towards characterizing and distinguishing this new signaling pathway for drug discovery. Here, we summarize recent advances that address the beta-arrestin signaling in the cardiovascular system, focusing on the activation of the AT1R.
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