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ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19

At the end of 2019, the coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in China. Currently, it is breaking out globally and posing a serious threat to public health. The typically clinical characteristics of COVID-19 patients were...

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Autores principales: Dong, Mengzhen, Zhang, Jie, Ma, Xuefeng, Tan, Jie, Chen, Lizhen, Liu, Shousheng, Xin, Yongning, Zhuang, Likun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Masson SAS. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444942/
https://www.ncbi.nlm.nih.gov/pubmed/32861070
http://dx.doi.org/10.1016/j.biopha.2020.110678
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author Dong, Mengzhen
Zhang, Jie
Ma, Xuefeng
Tan, Jie
Chen, Lizhen
Liu, Shousheng
Xin, Yongning
Zhuang, Likun
author_facet Dong, Mengzhen
Zhang, Jie
Ma, Xuefeng
Tan, Jie
Chen, Lizhen
Liu, Shousheng
Xin, Yongning
Zhuang, Likun
author_sort Dong, Mengzhen
collection PubMed
description At the end of 2019, the coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in China. Currently, it is breaking out globally and posing a serious threat to public health. The typically clinical characteristics of COVID-19 patients were fever and respiratory symptoms, and a proportion of patients were accompanied by extrapulmonary symptoms including cardiac injury, kidney injury, liver injury, digestive tract injury, and neurological symptoms. Angiotensin converting enzyme 2 (ACE2) has been proven to be a major receptor for SARS-CoV-2 and could mediate virus entry into cells. And transmembrane protease serine 2 (TMPRSS2) could cleave the spike (S) protein of SARS-CoV-2, which facilitates the fusion of SARS-CoV-2 and cellular membranes. The mRNA expressions of both ACE2 and TMPRSS2 were observed in the heart, digestive tract, liver, kidney, brain and other organs. SARS-CoV-2 may have a capacity to infect extrapulmonary organs due to the expressions of ACE2 and TMPRSS2 in the cells and tissues of these organs. It seems that there is a potential involvement of ACE2 and TMPRSS2 expressions in the virus infection of extrapulmonary organs and the manifestation of symptoms related to these organs in patients with COVID-19. Here, we revealed the expressions of ACE2 and TMPRSS2 in extrapulmonary organs, and we also summarized the clinical manifestation and the management of extrapulmonary complications in patients with COVID-19.
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spelling pubmed-74449422020-08-26 ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19 Dong, Mengzhen Zhang, Jie Ma, Xuefeng Tan, Jie Chen, Lizhen Liu, Shousheng Xin, Yongning Zhuang, Likun Biomed Pharmacother Review At the end of 2019, the coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in China. Currently, it is breaking out globally and posing a serious threat to public health. The typically clinical characteristics of COVID-19 patients were fever and respiratory symptoms, and a proportion of patients were accompanied by extrapulmonary symptoms including cardiac injury, kidney injury, liver injury, digestive tract injury, and neurological symptoms. Angiotensin converting enzyme 2 (ACE2) has been proven to be a major receptor for SARS-CoV-2 and could mediate virus entry into cells. And transmembrane protease serine 2 (TMPRSS2) could cleave the spike (S) protein of SARS-CoV-2, which facilitates the fusion of SARS-CoV-2 and cellular membranes. The mRNA expressions of both ACE2 and TMPRSS2 were observed in the heart, digestive tract, liver, kidney, brain and other organs. SARS-CoV-2 may have a capacity to infect extrapulmonary organs due to the expressions of ACE2 and TMPRSS2 in the cells and tissues of these organs. It seems that there is a potential involvement of ACE2 and TMPRSS2 expressions in the virus infection of extrapulmonary organs and the manifestation of symptoms related to these organs in patients with COVID-19. Here, we revealed the expressions of ACE2 and TMPRSS2 in extrapulmonary organs, and we also summarized the clinical manifestation and the management of extrapulmonary complications in patients with COVID-19. The Authors. Published by Elsevier Masson SAS. 2020-11 2020-08-24 /pmc/articles/PMC7444942/ /pubmed/32861070 http://dx.doi.org/10.1016/j.biopha.2020.110678 Text en © 2020 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Dong, Mengzhen
Zhang, Jie
Ma, Xuefeng
Tan, Jie
Chen, Lizhen
Liu, Shousheng
Xin, Yongning
Zhuang, Likun
ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19
title ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19
title_full ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19
title_fullStr ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19
title_full_unstemmed ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19
title_short ACE2, TMPRSS2 distribution and extrapulmonary organ injury in patients with COVID-19
title_sort ace2, tmprss2 distribution and extrapulmonary organ injury in patients with covid-19
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444942/
https://www.ncbi.nlm.nih.gov/pubmed/32861070
http://dx.doi.org/10.1016/j.biopha.2020.110678
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