COVID-19: angiotensin-converting enzyme 2 (ACE2) expression and tissue susceptibility to SARS-CoV-2 infection

被引:0
作者
Stephany Beyerstedt
Expedito Barbosa Casaro
Érika Bevilaqua Rangel
机构
[1] Hospital Israelita Albert Einstein,Albert Einstein Research and Education Institute
[2] Federal University of São Paulo,Nephrology Division
来源
European Journal of Clinical Microbiology & Infectious Diseases | 2021年 / 40卷
关键词
Angiotensin-converting enzyme; COVID-19; SARS-CoV-2; Tissue damage;
D O I
暂无
中图分类号
学科分类号
摘要
COVID-19 pandemic is caused by the novel coronavirus SARS-CoV-2. Angiotensin-converting enzyme 2 (ACE2) is not only an enzyme but also a functional receptor on cell surfaces through which SARS-CoV-2 enters the host cells and is highly expressed in the heart, kidneys, and lungs and shed into the plasma. ACE2 is a key regulator of the renin–angiotensin–aldosterone system (RAAS). SARS-CoV-2 causes ACE/ACE2 balance disruption and RAAS activation, which leads ultimately to COVID-19 progression, especially in patients with comorbidities, such as hypertension, diabetes mellitus, and cardiovascular disease. Therefore, ACE2 expression may have paradoxical effects, aiding SARS-CoV-2 pathogenicity, yet conversely limiting viral infection. This article reviews the existing literature and knowledge of ACE2 in COVID-19 setting and focuses on its pathophysiologic involvement in disease progression, clinical outcomes, and therapeutic potential.
引用
收藏
页码:905 / 919
页数:14
相关论文
共 1464 条
[1]  
Zhou P(2020)A pneumonia outbreak associated with a new coronavirus of probable bat origin Nature 579 270-273
[2]  
Yang XL(2003)Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus Nature 426 450-454
[3]  
Wang XG(2020)Characterization of the receptor-binding domain (RBD) of 2019 novel coronavirus: implication for development of RBD protein as a viral attachment inhibitor and vaccine Cellular & Molecular Immunology 17 613-620
[4]  
Hu B(2020)Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation Science 367 1260-280.e8
[5]  
Zhang L(2020)SARS-CoV-2 induces transcriptional signatures in human lung epithelial cells that promote lung fibrosis Respiratory Research 21 182-261
[6]  
Zhang W(2020)SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor Cell 181 271-536
[7]  
Si HR(2016)Structure, function, and evolution of coronavirus spike proteins Annual Review of Virology 3 237-856
[8]  
Zhu Y(2009)Devil and angel in the renin-angiotensin system: ACE-angiotensin II-AT1 receptor axis vs. ACE2-angiotensin-(1-7)-Mas receptor axis Hypertension Research: Official Journal of the Japanese Society of Hypertension 32 533-e89
[9]  
Li B(2020)Downregulation of ACE2 induces overstimulation of the renin–angiotensin system in COVID-19: should we block the renin–angiotensin system? Hypertension Research 43 854-33243
[10]  
Huang CL(2020)Binding of SARS-CoV-2 and angiotensin-converting enzyme 2: clinical implications Cardiovascular Research 116 e87-68