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SARS‐CoV‐2 research using human pluripotent stem cells and organoids

Experimental cell models are indispensable for clarifying the pathophysiology of coronavirus disease 2019 (COVID‐19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection, and for developing therapeutic agents. To recapitulate the symptoms and drug response of CO...

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Autores principales: Deguchi, Sayaka, Serrano‐Aroca, Ángel, Tambuwala, Murtaza M., Uhal, Bruce D., Brufsky, Adam M., Takayama, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550698/
https://www.ncbi.nlm.nih.gov/pubmed/34302450
http://dx.doi.org/10.1002/sctm.21-0183
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author Deguchi, Sayaka
Serrano‐Aroca, Ángel
Tambuwala, Murtaza M.
Uhal, Bruce D.
Brufsky, Adam M.
Takayama, Kazuo
author_facet Deguchi, Sayaka
Serrano‐Aroca, Ángel
Tambuwala, Murtaza M.
Uhal, Bruce D.
Brufsky, Adam M.
Takayama, Kazuo
author_sort Deguchi, Sayaka
collection PubMed
description Experimental cell models are indispensable for clarifying the pathophysiology of coronavirus disease 2019 (COVID‐19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection, and for developing therapeutic agents. To recapitulate the symptoms and drug response of COVID‐19 patients in vitro, SARS‐CoV‐2 studies using physiologically relevant human embryonic stem (ES)/induced pluripotent stem (iPS) cell‐derived somatic cells and organoids are ongoing. These cells and organoids have been used to show that SARS‐CoV‐2 can infect and damage various organs including the lung, heart, brain, intestinal tract, kidney, and pancreas. They are also being used to develop COVID‐19 therapeutic agents, including evaluation of their antiviral efficacy and safety. The relationship between COVID‐19 aggravation and human genetic backgrounds has been investigated using genetically modified ES/iPS cells and patient‐derived iPS cells. This review summarizes the latest results and issues of SARS‐CoV‐2 research using human ES/iPS cell‐derived somatic cells and organoids.
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spelling pubmed-85506982021-11-04 SARS‐CoV‐2 research using human pluripotent stem cells and organoids Deguchi, Sayaka Serrano‐Aroca, Ángel Tambuwala, Murtaza M. Uhal, Bruce D. Brufsky, Adam M. Takayama, Kazuo Stem Cells Transl Med Concise Reviews Experimental cell models are indispensable for clarifying the pathophysiology of coronavirus disease 2019 (COVID‐19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection, and for developing therapeutic agents. To recapitulate the symptoms and drug response of COVID‐19 patients in vitro, SARS‐CoV‐2 studies using physiologically relevant human embryonic stem (ES)/induced pluripotent stem (iPS) cell‐derived somatic cells and organoids are ongoing. These cells and organoids have been used to show that SARS‐CoV‐2 can infect and damage various organs including the lung, heart, brain, intestinal tract, kidney, and pancreas. They are also being used to develop COVID‐19 therapeutic agents, including evaluation of their antiviral efficacy and safety. The relationship between COVID‐19 aggravation and human genetic backgrounds has been investigated using genetically modified ES/iPS cells and patient‐derived iPS cells. This review summarizes the latest results and issues of SARS‐CoV‐2 research using human ES/iPS cell‐derived somatic cells and organoids. John Wiley & Sons, Inc. 2021-07-24 /pmc/articles/PMC8550698/ /pubmed/34302450 http://dx.doi.org/10.1002/sctm.21-0183 Text en © 2021 The Authors. stem cells translational medicine published by Wiley Periodicals LLC on behalf of AlphaMed Press. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Concise Reviews
Deguchi, Sayaka
Serrano‐Aroca, Ángel
Tambuwala, Murtaza M.
Uhal, Bruce D.
Brufsky, Adam M.
Takayama, Kazuo
SARS‐CoV‐2 research using human pluripotent stem cells and organoids
title SARS‐CoV‐2 research using human pluripotent stem cells and organoids
title_full SARS‐CoV‐2 research using human pluripotent stem cells and organoids
title_fullStr SARS‐CoV‐2 research using human pluripotent stem cells and organoids
title_full_unstemmed SARS‐CoV‐2 research using human pluripotent stem cells and organoids
title_short SARS‐CoV‐2 research using human pluripotent stem cells and organoids
title_sort sars‐cov‐2 research using human pluripotent stem cells and organoids
topic Concise Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550698/
https://www.ncbi.nlm.nih.gov/pubmed/34302450
http://dx.doi.org/10.1002/sctm.21-0183
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