疾病
糖尿病
生物
调节器
肾素-血管紧张素系统
血管紧张素转化酶2
生物信息学
血压
病态的
醛固酮
受体
心血管生理学
功能(生物学)
肾
医学
内分泌学
内科学
生理学
2019年冠状病毒病(COVID-19)
细胞生物学
基因
遗传学
传染病(医学专业)
作者
Inge Hamming,M. E. Cooper,Bart L. Haagmans,Nigel M. Hooper,Ron Korstanje,ADME Osterhaus,Wim Timens,AJ Turner,G. Navis,Harry van Goor
摘要
Abstract The renin–angiotensin–aldosterone system (RAAS) is a key regulator of systemic blood pressure and renal function and a key player in renal and cardiovascular disease. However, its (patho)physiological roles and its architecture are more complex than initially anticipated. Novel RAAS components that may add to our understanding have been discovered in recent years. In particular, the human homologue of ACE (ACE2) has added a higher level of complexity to the RAAS. In a short period of time, ACE2 has been cloned, purified, knocked‐out, knocked‐in; inhibitors have been developed; its 3D structure determined; and new functions have been identified. ACE2 is now implicated in cardiovascular and renal (patho)physiology, diabetes, pregnancy, lung disease and, remarkably, ACE2 serves as a receptor for SARS and NL63 coronaviruses. This review covers available information on the genetic, structural and functional properties of ACE2. Its role in a variety of (patho)physiological conditions and therapeutic options of modulation are discussed. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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