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Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells
Genetic differences are a primary reason for differences in the susceptibility and severity of COVID-19. As induced pluripotent stem (iPS) cells maintain the genetic information of the donor, they can be used to model individual differences in SARS-CoV-2 infection in vitro. We found that human iPS c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051014/ https://www.ncbi.nlm.nih.gov/pubmed/33880436 http://dx.doi.org/10.1016/j.isci.2021.102428 |
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author | Sano, Emi Deguchi, Sayaka Sakamoto, Ayaka Mimura, Natsumi Hirabayashi, Ai Muramoto, Yukiko Noda, Takeshi Yamamoto, Takuya Takayama, Kazuo |
author_facet | Sano, Emi Deguchi, Sayaka Sakamoto, Ayaka Mimura, Natsumi Hirabayashi, Ai Muramoto, Yukiko Noda, Takeshi Yamamoto, Takuya Takayama, Kazuo |
author_sort | Sano, Emi |
collection | PubMed |
description | Genetic differences are a primary reason for differences in the susceptibility and severity of COVID-19. As induced pluripotent stem (iPS) cells maintain the genetic information of the donor, they can be used to model individual differences in SARS-CoV-2 infection in vitro. We found that human iPS cells expressing the SARS-CoV-2 receptor angiotensin-converting enzyme 2 (ACE2) (ACE2-iPS cells) can be infected w SARS-CoV-2. In infected ACE2-iPS cells, the expression of SARS-CoV-2 nucleocapsid protein, budding of viral particles, and production of progeny virus, double membrane spherules, and double-membrane vesicles were confirmed. We performed SARS-CoV-2 infection experiments on ACE2-iPS/ embryonic stem (ES) cells from eight individuals. Male iPS/ES cells were more capable of producing the virus compared with female iPS/ES cells. These findings suggest that ACE2-iPS cells can not only reproduce individual differences in SARS-CoV-2 infection in vitro but also are a useful resource to clarify the causes of individual differences in COVID-19 due to genetic differences. |
format | Online Article Text |
id | pubmed-8051014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80510142021-04-16 Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells Sano, Emi Deguchi, Sayaka Sakamoto, Ayaka Mimura, Natsumi Hirabayashi, Ai Muramoto, Yukiko Noda, Takeshi Yamamoto, Takuya Takayama, Kazuo iScience Article Genetic differences are a primary reason for differences in the susceptibility and severity of COVID-19. As induced pluripotent stem (iPS) cells maintain the genetic information of the donor, they can be used to model individual differences in SARS-CoV-2 infection in vitro. We found that human iPS cells expressing the SARS-CoV-2 receptor angiotensin-converting enzyme 2 (ACE2) (ACE2-iPS cells) can be infected w SARS-CoV-2. In infected ACE2-iPS cells, the expression of SARS-CoV-2 nucleocapsid protein, budding of viral particles, and production of progeny virus, double membrane spherules, and double-membrane vesicles were confirmed. We performed SARS-CoV-2 infection experiments on ACE2-iPS/ embryonic stem (ES) cells from eight individuals. Male iPS/ES cells were more capable of producing the virus compared with female iPS/ES cells. These findings suggest that ACE2-iPS cells can not only reproduce individual differences in SARS-CoV-2 infection in vitro but also are a useful resource to clarify the causes of individual differences in COVID-19 due to genetic differences. Elsevier 2021-04-16 /pmc/articles/PMC8051014/ /pubmed/33880436 http://dx.doi.org/10.1016/j.isci.2021.102428 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Sano, Emi Deguchi, Sayaka Sakamoto, Ayaka Mimura, Natsumi Hirabayashi, Ai Muramoto, Yukiko Noda, Takeshi Yamamoto, Takuya Takayama, Kazuo Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells |
title | Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells |
title_full | Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells |
title_fullStr | Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells |
title_full_unstemmed | Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells |
title_short | Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells |
title_sort | modeling sars-cov-2 infection and its individual differences with ace2-expressing human ips cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051014/ https://www.ncbi.nlm.nih.gov/pubmed/33880436 http://dx.doi.org/10.1016/j.isci.2021.102428 |
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