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Heterogeneous expression of ACE2 and TMPRRS2 in mesenchymal stromal cells.
Generali, Melanie; Kehl, Debora; Wanner, Debora; Okoniewski, Michal J; Hoerstrup, Simon P; Cinelli, Paolo.
Afiliação
  • Generali M; Institute for Regenerative Medicine (IREM), Center for Therapy Development and Good Manufacturing Practice, University of Zurich, Zurich, Switzerland.
  • Kehl D; Institute for Regenerative Medicine (IREM), Center for Therapy Development and Good Manufacturing Practice, University of Zurich, Zurich, Switzerland.
  • Wanner D; Institute for Regenerative Medicine (IREM), Center for Therapy Development and Good Manufacturing Practice, University of Zurich, Zurich, Switzerland.
  • Okoniewski MJ; Scientific IT Services ETH Zurich, ETH Zurich, Zürich, Switzerland.
  • Hoerstrup SP; Institute for Regenerative Medicine (IREM), Center for Therapy Development and Good Manufacturing Practice, University of Zurich, Zurich, Switzerland.
  • Cinelli P; Center for Applied Biotechnology and Molecular Medicine (CABMM), University of Zurich, Zurich, Switzerland.
J Cell Mol Med ; 26(1): 228-234, 2022 01.
Article em En | MEDLINE | ID: mdl-34821008
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Mesenquimais / Glicoproteína da Espícula de Coronavírus / Terapia Baseada em Transplante de Células e Tecidos / Síndrome da Liberação de Citocina / Enzima de Conversão de Angiotensina 2 / SARS-CoV-2 / COVID-19 Limite: Humans Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Mesenquimais / Glicoproteína da Espícula de Coronavírus / Terapia Baseada em Transplante de Células e Tecidos / Síndrome da Liberação de Citocina / Enzima de Conversão de Angiotensina 2 / SARS-CoV-2 / COVID-19 Limite: Humans Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça