Angiotensin-converting enzyme 2 in acute respiratory distress syndrome

被引:0
|
作者
Y. Imai
K. Kuba
J. M. Penninger
机构
[1] Institute of Molecular Biotechnology of the Austrian Academy of Sciences,IMBA
来源
Cellular and Molecular Life Sciences | 2007年 / 64卷
关键词
Renin-angiotensin system (RAS); angiotensin; angiotensin-converting enzyme 2 (ACE2); ACE; acute respiratory distress syndrome (ARDS); severe acute respiratory syndrome (SARS);
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学科分类号
摘要
Angiotensin-converting enzyme (ACE) and ACE2 are highly homologous metalloproteases that provide essential catalytic functions in the renin-angiotensin system (RAS). Angiotensin II is one key effector peptide of the RAS, inducing vasoconstriction and exerting multiple biological functions. ACE cleaves angiotensin I to generate angiotensin II, whereas ACE2 reduces angiotensin II levels. Accumulating evidence has demonstrated a physiological and pathological role of ACE2 in the cardiovascular systems. Intriguingly, the SARS coronavirus, the cause of severe acute respiratory syndrome (SARS), utilizes ACE2 as an essential receptor for cell fusion and in vivo infections. Moreover, recent studies have demonstrated that ACE2 protects murine lungs from acute lung injury as well as SARS-Spike protein-mediated lung injury, suggesting a dual role of ACE2 in SARS infections and protection from ARDS.
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页码:2006 / 2012
页数:6
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