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Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells
Coronavirus disease (COVID-19) is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). SARS-CoV-2 RNA has been found in the human testis on occasion, but subgenomic SARS-CoV-2 and infectious SARS-CoV-2 virions have not been found. There is no direct evidence of SARS-CoV-2 infectio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083717/ https://www.ncbi.nlm.nih.gov/pubmed/37026452 http://dx.doi.org/10.1369/00221554231168916 |
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author | Ribeiro, Maria Rita Calado, Ana Margarida Alves, Ângela Pereira, Rute Sousa, Mário Sá, Rosália |
author_facet | Ribeiro, Maria Rita Calado, Ana Margarida Alves, Ângela Pereira, Rute Sousa, Mário Sá, Rosália |
author_sort | Ribeiro, Maria Rita |
collection | PubMed |
description | Coronavirus disease (COVID-19) is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). SARS-CoV-2 RNA has been found in the human testis on occasion, but subgenomic SARS-CoV-2 and infectious SARS-CoV-2 virions have not been found. There is no direct evidence of SARS-CoV-2 infection of testicular cells. To better understand this, it is necessary to determine whether SARS-CoV-2 receptors and proteases are present in testicular cells. To overcome this limitation, we focused on elucidating with immunohistochemistry the spatial distribution of the SARS-CoV-2 receptors angiotensin-converting enzyme 2 (ACE2) and cluster of differentiation 147 (CD147), as well as their viral spike protein priming proteases, transmembrane protease serine 2 (TMPRSS2) and cathepsin L (CTSL), required for viral fusion with host cells. At the protein level, human testicular tissue expressed both receptors and proteases studied. Both ACE2 and TMPRSS2 were found in interstitial cells (endothelium, Leydig, and myoid peritubular cells) and in the seminiferous epithelium (Sertoli cells, spermatogonia, spermatocytes, and spermatids). The presence of CD147 was observed in all cell types except endothelium and peritubular cells, while CTSL was exclusively observed in Leydig, peritubular, and Sertoli cells. These findings show that the ACE2 receptor and its protease TMPRSS2 are coexpressed in all testicular cells, as well as the CD147 receptor and its protease CTSL in Leydig and Sertoli cells, indicating that testicular SARS-CoV-2 infection cannot be ruled out without further investigation: |
format | Online Article Text |
id | pubmed-10083717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-100837172023-04-11 Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells Ribeiro, Maria Rita Calado, Ana Margarida Alves, Ângela Pereira, Rute Sousa, Mário Sá, Rosália J Histochem Cytochem Articles Coronavirus disease (COVID-19) is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). SARS-CoV-2 RNA has been found in the human testis on occasion, but subgenomic SARS-CoV-2 and infectious SARS-CoV-2 virions have not been found. There is no direct evidence of SARS-CoV-2 infection of testicular cells. To better understand this, it is necessary to determine whether SARS-CoV-2 receptors and proteases are present in testicular cells. To overcome this limitation, we focused on elucidating with immunohistochemistry the spatial distribution of the SARS-CoV-2 receptors angiotensin-converting enzyme 2 (ACE2) and cluster of differentiation 147 (CD147), as well as their viral spike protein priming proteases, transmembrane protease serine 2 (TMPRSS2) and cathepsin L (CTSL), required for viral fusion with host cells. At the protein level, human testicular tissue expressed both receptors and proteases studied. Both ACE2 and TMPRSS2 were found in interstitial cells (endothelium, Leydig, and myoid peritubular cells) and in the seminiferous epithelium (Sertoli cells, spermatogonia, spermatocytes, and spermatids). The presence of CD147 was observed in all cell types except endothelium and peritubular cells, while CTSL was exclusively observed in Leydig, peritubular, and Sertoli cells. These findings show that the ACE2 receptor and its protease TMPRSS2 are coexpressed in all testicular cells, as well as the CD147 receptor and its protease CTSL in Leydig and Sertoli cells, indicating that testicular SARS-CoV-2 infection cannot be ruled out without further investigation: SAGE Publications 2023-04-07 2023-04 /pmc/articles/PMC10083717/ /pubmed/37026452 http://dx.doi.org/10.1369/00221554231168916 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Articles Ribeiro, Maria Rita Calado, Ana Margarida Alves, Ângela Pereira, Rute Sousa, Mário Sá, Rosália Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells |
title | Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells |
title_full | Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells |
title_fullStr | Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells |
title_full_unstemmed | Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells |
title_short | Spatial Distribution of SARS-CoV-2 Receptors and Proteases in Testicular Cells |
title_sort | spatial distribution of sars-cov-2 receptors and proteases in testicular cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083717/ https://www.ncbi.nlm.nih.gov/pubmed/37026452 http://dx.doi.org/10.1369/00221554231168916 |
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