SARS-CoV-2 Entry Receptor ACE2 Is Expressed on Very Small CD45


Journal

Stem cell reviews and reports
ISSN: 2629-3277
Titre abrégé: Stem Cell Rev Rep
Pays: United States
ID NLM: 101752767

Informations de publication

Date de publication:
02 2021
Historique:
pubmed: 22 7 2020
medline: 3 3 2021
entrez: 22 7 2020
Statut: ppublish

Résumé

Angiotensin-converting enzyme 2 (ACE2) plays an important role as a member of the renin-angiotensin-aldosterone system (RAAS) in regulating the conversion of angiotensin II (Ang II) into angiotensin (1-7) (Ang [1-7]). But at the same time, while expressed on the surface of human cells, ACE2 is the entry receptor for SARS-CoV-2. Expression of this receptor has been described in several types of cells, including hematopoietic stem cells (HSCs) and endothelial progenitor cells (EPCs), which raises a concern that the virus may infect and damage the stem cell compartment. We demonstrate for the first time that ACE2 and the entry-facilitating transmembrane protease TMPRSS2 are expressed on very small CD133

Identifiants

pubmed: 32691370
doi: 10.1007/s12015-020-10010-z
pii: 10.1007/s12015-020-10010-z
pmc: PMC7370872
doi:

Substances chimiques

Inflammasomes 0
NLR Family, Pyrin Domain-Containing 3 Protein 0
NLRP3 protein, human 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0
Leukocyte Common Antigens EC 3.1.3.48
ACE2 protein, human EC 3.4.17.23
Angiotensin-Converting Enzyme 2 EC 3.4.17.23
Serine Endopeptidases EC 3.4.21.-
TMPRSS2 protein, human EC 3.4.21.-

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

266-277

Subventions

Organisme : NIH HHS
ID : 2R01 DK074720
Pays : United States

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Auteurs

Mariusz Z Ratajczak (MZ)

Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, 500 S. Floyd Street, Rm. 107, Louisville, KY, 40202, USA. mzrata01@louisville.edu.
Department of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland. mzrata01@louisville.edu.

Kamila Bujko (K)

Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, 500 S. Floyd Street, Rm. 107, Louisville, KY, 40202, USA.

Andrzej Ciechanowicz (A)

Department of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland.

Kasia Sielatycka (K)

Institute of Biology, Faculty of Exact and Natural Sciences, University of Szczecin, Szczecin, Poland.
Research and Developmental Center Sanprobi, Szczecin, Poland.

Monika Cymer (M)

Department of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland.

Wojciech Marlicz (W)

Research and Developmental Center Sanprobi, Szczecin, Poland.

Magda Kucia (M)

Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, 500 S. Floyd Street, Rm. 107, Louisville, KY, 40202, USA. mjkuci01@louisville.edu.
Department of Regenerative Medicine, Center for Preclinical Research and Technology, Medical University of Warsaw, Warsaw, Poland. mjkuci01@louisville.edu.

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Classifications MeSH