The SARS-CoV2 - ACE2 link: a physiopathological analysis

Q4 Neuroscience Vascular Cell Pub Date : 2020-08-03 DOI:10.24238/13221-12-1-197
E. Petcu, C. Andry, E. Burks, S. Hamlet, E. Janssen, K. Kjellevold, A. Morenas, N. Miller, R. Miroiu, I. Nusem, A. Popa-Wagner
{"title":"The SARS-CoV2 - ACE2 link: a physiopathological analysis","authors":"E. Petcu, C. Andry, E. Burks, S. Hamlet, E. Janssen, K. Kjellevold, A. Morenas, N. Miller, R. Miroiu, I. Nusem, A. Popa-Wagner","doi":"10.24238/13221-12-1-197","DOIUrl":null,"url":null,"abstract":"The Covid-19 pandemic represents an unsolved problem which has caused numerous fatalities At the present time, there is no vaccination available or curative therapy However, recent reports suggest that SARS-CoV2 acts upon its functional receptor ACE2 inducing a variety of deleterious effects such as inflammation, endothelial dysfunction, microangiopathy, myocarditis, thrombosis and myocardial infarction The details of the SARS-CoV2-ACE2 interaction are poorly understood and most of the hypothesis related to this are based on the extrapolation of previous research focusing on ACE2 as a receptor for SARS-CoV Considering the similarities between SARS-CoV2 and SARS-CoV we have conducted a physiopathological analysis focusing on the key pathogenic role of ACE2 as a functional receptor for SARS-CoV2 In this context, we have identified several potential therapeutic targets which should be further evaluated in patients with Covid-19 It is likely that an efficient therapy for Covid-19 will be revealed by research investigating the binding of viral spike S protein to ACE2, and the immunological response determined by SARS-CoV2-ACE2 interaction, including the anti-viral role of plasmacytoid dendritic cells and anti-inflammatory reprogramming of macrophages © Eugen B Petcu, Christopher Andry, Eric J Burks, Stephen Hamlet, Emiel AM Janssen, Kjell H Kjellevold, Antonio de Las Morenas, Nancy S Miller, Rodica I Miroiu, Iulian Nusem, Aurel Popa-Wagner","PeriodicalId":23948,"journal":{"name":"Vascular Cell","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vascular Cell","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24238/13221-12-1-197","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 1

Abstract

The Covid-19 pandemic represents an unsolved problem which has caused numerous fatalities At the present time, there is no vaccination available or curative therapy However, recent reports suggest that SARS-CoV2 acts upon its functional receptor ACE2 inducing a variety of deleterious effects such as inflammation, endothelial dysfunction, microangiopathy, myocarditis, thrombosis and myocardial infarction The details of the SARS-CoV2-ACE2 interaction are poorly understood and most of the hypothesis related to this are based on the extrapolation of previous research focusing on ACE2 as a receptor for SARS-CoV Considering the similarities between SARS-CoV2 and SARS-CoV we have conducted a physiopathological analysis focusing on the key pathogenic role of ACE2 as a functional receptor for SARS-CoV2 In this context, we have identified several potential therapeutic targets which should be further evaluated in patients with Covid-19 It is likely that an efficient therapy for Covid-19 will be revealed by research investigating the binding of viral spike S protein to ACE2, and the immunological response determined by SARS-CoV2-ACE2 interaction, including the anti-viral role of plasmacytoid dendritic cells and anti-inflammatory reprogramming of macrophages © Eugen B Petcu, Christopher Andry, Eric J Burks, Stephen Hamlet, Emiel AM Janssen, Kjell H Kjellevold, Antonio de Las Morenas, Nancy S Miller, Rodica I Miroiu, Iulian Nusem, Aurel Popa-Wagner
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
SARS-CoV2 - ACE2联系:生理病理分析
Covid-19大流行是一个尚未解决的问题,已造成大量死亡。目前,没有可用的疫苗或治愈性治疗方法。然而,最近的报告表明,SARS-CoV2作用于其功能性受体ACE2,诱导多种有害影响,如炎症、内皮功能障碍、微血管病变、心肌炎、SARS-CoV2-ACE2相互作用的细节尚不清楚,与此相关的大多数假设都是基于以往关注ACE2作为SARS-CoV受体的研究的外推。考虑到SARS-CoV2和SARS-CoV之间的相似性,我们对ACE2作为SARS-CoV2的功能受体的关键致病作用进行了生理病理分析。我们已经确定了几个潜在的治疗靶点,这些靶点应该在Covid-19患者中进一步评估。通过研究病毒刺突S蛋白与ACE2的结合,以及SARS-CoV2-ACE2相互作用决定的免疫反应,包括浆细胞样树突状细胞的抗病毒作用和巨噬细胞的抗炎重编程,可能会发现一种有效的Covid-19治疗方法©Eugen B Petcu, Christopher Andry, Eric J Burks,斯蒂芬·哈姆雷特、埃米尔·扬森、谢尔·H·谢尔莱沃尔德、安东尼奥·德·拉斯·莫雷纳斯、南希·S·米勒、罗迪卡·米罗尤、尤利安·努瑟姆、奥雷尔·波普-瓦格纳
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Vascular Cell
Vascular Cell Neuroscience-Neurology
CiteScore
0.70
自引率
0.00%
发文量
0
期刊最新文献
A 3-Dimensional Hypothesis of Oxidative Phosphorylation The long and winding road: detecting and quantifying Notch activation in endothelial cells Vascular Tumors Result from Adeno-Associated Virus-9 Angiogenic Gene Therapy of Bone Allografts A clinically relevant model of stroke using aged rats The SARS-CoV2 - ACE2 link: a physiopathological analysis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1