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Age- and gender-related difference of ACE2 expression in rat lung
Epidemiologic data suggested that there was an obvious predominance of young adult patients with a slight female proneness in severe acute respiratory syndrome (SARS). The angiotensin-converting enzyme 2 (ACE2) was very recently identified as a functional receptor for SARS virus and is therefore a p...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094566/ https://www.ncbi.nlm.nih.gov/pubmed/16303146 http://dx.doi.org/10.1016/j.lfs.2005.09.038 |
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author | Xudong, Xie Junzhu, Chen Xingxiang, Wang Furong, Zhang Yanrong, Liu |
author_facet | Xudong, Xie Junzhu, Chen Xingxiang, Wang Furong, Zhang Yanrong, Liu |
author_sort | Xudong, Xie |
collection | PubMed |
description | Epidemiologic data suggested that there was an obvious predominance of young adult patients with a slight female proneness in severe acute respiratory syndrome (SARS). The angiotensin-converting enzyme 2 (ACE2) was very recently identified as a functional receptor for SARS virus and is therefore a prime target for pathogenesis and pharmacological intervention. Rats of both genders at three distinct ages (young-adult, 3 months; middle-aged, 12 months; old, 24 months) were evaluated to determine the characteristic of ACE2 expression in lung and the effect of aging and gender on its expression. ACE2 was predominantly expressed in alveolar epithelium, bronchiolar epithelium, endothelium and smooth muscle cells of pulmonary vessels with similar content, whereas no obvious signal was detected in the bronchiolar smooth muscle cells. ACE2 expression is dramatically reduced with aging in both genders: young-adult vs. old P < 0.001 (by 78% in male and 67% in female, respectively) and middle-aged vs. old P < 0.001 (by 71% in male rats and 59% in female rats, respectively). The decrease of ACE2 content was relatively slight between young-adult and middle-aged groups (by 25% in male and 18% in female, respectively). Although there was no gender-related difference of ACE2 in young-adult and middle-aged groups, a significantly higher ACE2 content was detected in old female rats than male. In conclusion, the more elevated ACE2 in young adults as compared to aged groups may contribute to the predominance in SARS attacks in this age group. |
format | Online Article Text |
id | pubmed-7094566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70945662020-03-25 Age- and gender-related difference of ACE2 expression in rat lung Xudong, Xie Junzhu, Chen Xingxiang, Wang Furong, Zhang Yanrong, Liu Life Sci Article Epidemiologic data suggested that there was an obvious predominance of young adult patients with a slight female proneness in severe acute respiratory syndrome (SARS). The angiotensin-converting enzyme 2 (ACE2) was very recently identified as a functional receptor for SARS virus and is therefore a prime target for pathogenesis and pharmacological intervention. Rats of both genders at three distinct ages (young-adult, 3 months; middle-aged, 12 months; old, 24 months) were evaluated to determine the characteristic of ACE2 expression in lung and the effect of aging and gender on its expression. ACE2 was predominantly expressed in alveolar epithelium, bronchiolar epithelium, endothelium and smooth muscle cells of pulmonary vessels with similar content, whereas no obvious signal was detected in the bronchiolar smooth muscle cells. ACE2 expression is dramatically reduced with aging in both genders: young-adult vs. old P < 0.001 (by 78% in male and 67% in female, respectively) and middle-aged vs. old P < 0.001 (by 71% in male rats and 59% in female rats, respectively). The decrease of ACE2 content was relatively slight between young-adult and middle-aged groups (by 25% in male and 18% in female, respectively). Although there was no gender-related difference of ACE2 in young-adult and middle-aged groups, a significantly higher ACE2 content was detected in old female rats than male. In conclusion, the more elevated ACE2 in young adults as compared to aged groups may contribute to the predominance in SARS attacks in this age group. Elsevier Inc. 2006-04-04 2005-11-21 /pmc/articles/PMC7094566/ /pubmed/16303146 http://dx.doi.org/10.1016/j.lfs.2005.09.038 Text en Copyright © 2005 Elsevier Inc. All rights reserved. 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 | Article Xudong, Xie Junzhu, Chen Xingxiang, Wang Furong, Zhang Yanrong, Liu Age- and gender-related difference of ACE2 expression in rat lung |
title | Age- and gender-related difference of ACE2 expression in rat lung |
title_full | Age- and gender-related difference of ACE2 expression in rat lung |
title_fullStr | Age- and gender-related difference of ACE2 expression in rat lung |
title_full_unstemmed | Age- and gender-related difference of ACE2 expression in rat lung |
title_short | Age- and gender-related difference of ACE2 expression in rat lung |
title_sort | age- and gender-related difference of ace2 expression in rat lung |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094566/ https://www.ncbi.nlm.nih.gov/pubmed/16303146 http://dx.doi.org/10.1016/j.lfs.2005.09.038 |
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