Cargando…

Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells

The outbreak of COVID‐19 has become a serious public health emergency. The virus targets cells by binding the ACE2 receptor. After infection, the virus triggers in some humans an immune storm containing the release of proinflammatory cytokines and chemokines followed by multiple organ failure. Sever...

Descripción completa

Detalles Bibliográficos
Autores principales: Generali, Melanie, Kehl, Debora, Wanner, Debora, Okoniewski, Michal J., Hoerstrup, Simon P., Cinelli, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742235/
https://www.ncbi.nlm.nih.gov/pubmed/34821008
http://dx.doi.org/10.1111/jcmm.17048
_version_ 1784629674193715200
author Generali, Melanie
Kehl, Debora
Wanner, Debora
Okoniewski, Michal J.
Hoerstrup, Simon P.
Cinelli, Paolo
author_facet Generali, Melanie
Kehl, Debora
Wanner, Debora
Okoniewski, Michal J.
Hoerstrup, Simon P.
Cinelli, Paolo
author_sort Generali, Melanie
collection PubMed
description The outbreak of COVID‐19 has become a serious public health emergency. The virus targets cells by binding the ACE2 receptor. After infection, the virus triggers in some humans an immune storm containing the release of proinflammatory cytokines and chemokines followed by multiple organ failure. Several vaccines are enrolled, but an effective treatment is still missing. Mesenchymal stem cells (MSCs) have shown to secrete immunomodulatory factors that suppress this cytokine storm. Therefore, MSCs have been suggested as a potential treatment option for COVID‐19. We report here that the ACE2 expression is minimal or nonexistent in MSC derived from three different human tissue sources (adipose tissue, umbilical cord Wharton`s jelly and bone marrow). In contrast, TMPRSS2 that is implicated in SARS‐CoV‐2 entry has been detected in all MSC samples. These results are of particular importance for future MSC‐based cell therapies to treat severe cases after COVID‐19 infection.
format Online
Article
Text
id pubmed-8742235
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-87422352022-01-12 Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells Generali, Melanie Kehl, Debora Wanner, Debora Okoniewski, Michal J. Hoerstrup, Simon P. Cinelli, Paolo J Cell Mol Med Short Communications The outbreak of COVID‐19 has become a serious public health emergency. The virus targets cells by binding the ACE2 receptor. After infection, the virus triggers in some humans an immune storm containing the release of proinflammatory cytokines and chemokines followed by multiple organ failure. Several vaccines are enrolled, but an effective treatment is still missing. Mesenchymal stem cells (MSCs) have shown to secrete immunomodulatory factors that suppress this cytokine storm. Therefore, MSCs have been suggested as a potential treatment option for COVID‐19. We report here that the ACE2 expression is minimal or nonexistent in MSC derived from three different human tissue sources (adipose tissue, umbilical cord Wharton`s jelly and bone marrow). In contrast, TMPRSS2 that is implicated in SARS‐CoV‐2 entry has been detected in all MSC samples. These results are of particular importance for future MSC‐based cell therapies to treat severe cases after COVID‐19 infection. John Wiley and Sons Inc. 2021-11-24 2022-01 /pmc/articles/PMC8742235/ /pubmed/34821008 http://dx.doi.org/10.1111/jcmm.17048 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Generali, Melanie
Kehl, Debora
Wanner, Debora
Okoniewski, Michal J.
Hoerstrup, Simon P.
Cinelli, Paolo
Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells
title Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells
title_full Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells
title_fullStr Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells
title_full_unstemmed Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells
title_short Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells
title_sort heterogeneous expression of ace2 and tmprrs2 in mesenchymal stromal cells
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742235/
https://www.ncbi.nlm.nih.gov/pubmed/34821008
http://dx.doi.org/10.1111/jcmm.17048
work_keys_str_mv AT generalimelanie heterogeneousexpressionoface2andtmprrs2inmesenchymalstromalcells
AT kehldebora heterogeneousexpressionoface2andtmprrs2inmesenchymalstromalcells
AT wannerdebora heterogeneousexpressionoface2andtmprrs2inmesenchymalstromalcells
AT okoniewskimichalj heterogeneousexpressionoface2andtmprrs2inmesenchymalstromalcells
AT hoerstrupsimonp heterogeneousexpressionoface2andtmprrs2inmesenchymalstromalcells
AT cinellipaolo heterogeneousexpressionoface2andtmprrs2inmesenchymalstromalcells