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Title: Modeling SARS-CoV-2 infection and its individual differences with ACE2-expressing human iPS cells
Authors: Sano, Emi
Deguchi, Sayaka
Sakamoto, Ayaka
Mimura, Natsumi
Hirabayashi, Ai
Muramoto, Yukiko  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-8706-3113 (unconfirmed)
Noda, Takeshi  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0658-4663 (unconfirmed)
Yamamoto, Takuya  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-0022-3947 (unconfirmed)
Takayama, Kazuo  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0002-1132-2457 (unconfirmed)
Author's alias: 佐野, 絵美
出口, 清香
坂本, 綾香
三村, 菜摘
平林, 愛
村本, 裕紀子
野田, 岳志
山本, 拓也
高山, 和雄
Keywords: Health Sciences
Virology
Cell Biology
Issue Date: May-2021
Publisher: Elsevier BV
Journal title: iScience
Volume: 24
Issue: 5
Thesis number: 102428
Abstract: 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.
Description: ACE発現ヒトiPS細胞を用いたSARS-CoV-2感染の個人差再現と原因究明. 京都大学プレスリリース. 2021-04-19.
Stem cells show gender differences in COVID-19 risk. 京都大学プレスリリース. 2021-04-19.
Rights: © 2021 The Author(s).
This is an open access article under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Public License.
URI: http://hdl.handle.net/2433/262724
DOI(Published Version): 10.1016/j.isci.2021.102428
PubMed ID: 33880436
Related Link: https://www.cira.kyoto-u.ac.jp/j/pressrelease/news/210419-000000.html
https://www.cira.kyoto-u.ac.jp/e/pressrelease/news/210419-000000.html
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