Suppr超能文献

血管紧张素转换酶2(ACE2):严重急性呼吸综合征冠状病毒2(SARS-CoV-2)受体和肾素-血管紧张素系统(RAS)调节剂

Angiotensin-converting enzyme 2 (ACE2): SARS-CoV-2 receptor and RAS modulator.

作者信息

Bian Jingwei, Li Zijian

机构信息

Department of Cardiology and Institute of Vascular Medicine, Peking University Third Hospital; Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Ministry of Health; Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education; Beijing Key Laboratory of Cardiovascular Receptors Research, Beijing 100191, China.

Department of Pharmacy, Peking University Third Hospital, Beijing 100191, China.

出版信息

Acta Pharm Sin B. 2021 Jan;11(1):1-12. doi: 10.1016/j.apsb.2020.10.006. Epub 2020 Oct 13.

Abstract

The coronavirus disease 2019 (COVID-19) outbreak is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Angiotensin-converting enzyme 2 (ACE2) was rapidly identified as the critical functional receptor for SARS-CoV-2. ACE2 is well-known as a counter-regulator of the renin-angiotensin system (RAS) and plays a key role in the cardiovascular system. Given that ACE2 functions as both a SARS-CoV-2 receptor and a RAS modulator, the treatment for COVID-19 presents a dilemma of how to limit virus entry but protect ACE2 physiological functions. Thus, an in-depth summary of the recent progress of ACE2 research and its relationship to the virus is urgently needed to provide possible solution to the dilemma. Here, we summarize the complexity and interplay between the coronavirus, ACE2 and RAS (including anti-RAS drugs). We propose five novel working modes for functional receptor for SARS-CoV-2 infection and the routes of ACE2-mediated virus entering host cells, as well as its regulatory mechanism. For the controversy of anti-RAS drugs application, we also give theoretical analysis and discussed for drug application. These will contribute to a deeper understanding of the complex mechanisms of underlying the relationship between the virus and ACE2, and provide guidance for virus intervention strategies.

摘要

2019冠状病毒病(COVID-19)疫情由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起。血管紧张素转换酶2(ACE2)很快被确定为SARS-CoV-2的关键功能受体。ACE2作为肾素-血管紧张素系统(RAS)的一种反调节因子广为人知,在心血管系统中起关键作用。鉴于ACE2既作为SARS-CoV-2受体又作为RAS调节剂发挥作用,COVID-19的治疗面临着如何限制病毒进入但又保护ACE2生理功能的两难境地。因此,迫切需要深入总结ACE2研究的最新进展及其与该病毒的关系,以提供解决这一两难困境的可能方案。在此,我们总结了冠状病毒、ACE2和RAS(包括抗RAS药物)之间的复杂性和相互作用。我们提出了SARS-CoV-2感染功能性受体的五种新工作模式、ACE2介导病毒进入宿主细胞的途径及其调控机制。对于抗RAS药物应用的争议,我们也进行了理论分析并讨论了药物应用问题。这些将有助于更深入地理解病毒与ACE2之间关系的复杂机制,并为病毒干预策略提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4459/7838025/b628f5e1ca0c/fx1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验