ACE2: The Major Cell Entry Receptor for SARS-CoV-2

被引:0
|
作者
Filippo Scialo
Aurora Daniele
Felice Amato
Lucio Pastore
Maria Gabriella Matera
Mario Cazzola
Giuseppe Castaldo
Andrea Bianco
机构
[1] University of Campania “L. Vanvitelli”,Dipartimento di Scienze Mediche Traslazionali
[2] University of Campania “L. Vanvitelli”,Dipartimento di Scienze e Tecnologie Ambientali Biologiche Farmaceutiche
[3] Università Di Napoli Federico II,Dipartimento di Medicina Molecolare e Biotecnologie Mediche
[4] CEINGE,Dipartimento di Medicina Sperimentale
[5] University of Campania “L. Vanvitelli”,Dipartimento di Medicina Sperimentale
[6] University of Rome “Tor Vergata”,undefined
来源
Lung | 2020年 / 198卷
关键词
SARS-CoV-2; ACE2 receptor; COVID-19;
D O I
暂无
中图分类号
学科分类号
摘要
Despite the unprecedented effort of the scientific community, the novel SARS-CoV-2 virus has infected more than 46 million people worldwide, killing over one million two hundred thousand. Understanding the mechanisms by which some individuals are more susceptible to SARS-CoV-2 infection and why a subgroup of them are prone to experience severe pneumonia, and death should lead to a better approach and more effective treatments for COVID-19. Here, we focus our attention on ACE2, a primary receptor of SARS-CoV-2. We will discuss its biology, tissue expression, and post-translational regulation that determine its potential to be employed by SARS-CoV-2 for cell entry. Particular attention will be given to how the ACE2 soluble form can have a great impact on disease progression and thus be used in a potential therapeutic strategy. Furthermore, we will discuss repercussions that SARS-CoV-2/ACE2 binding has on the renin–angiotensin system and beyond. Indeed, although mostly neglected, ACE2 can also act on [des-Arg 937]-bradykinin of the kinin–kallikrein system regulating coagulation and inflammation. Thorough comprehension of the role that ACE2 plays in different pathways will be the key to assess the impact that SARS-CoV-2/ACE2 binding has on organismal physiology and will help us to find better therapies and diagnostic tools.
引用
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页码:867 / 877
页数:10
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