Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1784591010915942400 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8550698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT deguchisayaka sarscov2researchusinghumanpluripotentstemcellsandorganoids AT serranoarocaangel sarscov2researchusinghumanpluripotentstemcellsandorganoids AT tambuwalamurtazam sarscov2researchusinghumanpluripotentstemcellsandorganoids AT uhalbruced sarscov2researchusinghumanpluripotentstemcellsandorganoids AT brufskyadamm sarscov2researchusinghumanpluripotentstemcellsandorganoids AT takayamakazuo sarscov2researchusinghumanpluripotentstemcellsandorganoids |