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Defense of COVID-19 by Human Organoids

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has created an immense menace to public health worldwide, exerting huge effects on global economic and political conditions. Understanding the biology and pathogenesis mechanisms of this nove...

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Autores principales: Lv, Ting, Meng, Fanlu, Yu, Meng, Huang, Haihui, Lin, Xinhua, Zhao, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277987/
https://www.ncbi.nlm.nih.gov/pubmed/35233559
http://dx.doi.org/10.1007/s43657-021-00015-0
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author Lv, Ting
Meng, Fanlu
Yu, Meng
Huang, Haihui
Lin, Xinhua
Zhao, Bing
author_facet Lv, Ting
Meng, Fanlu
Yu, Meng
Huang, Haihui
Lin, Xinhua
Zhao, Bing
author_sort Lv, Ting
collection PubMed
description Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has created an immense menace to public health worldwide, exerting huge effects on global economic and political conditions. Understanding the biology and pathogenesis mechanisms of this novel virus, in large parts, relies on optimal physiological models that allow replication and propagation of SARS-CoV-2. Human organoids, derived from stem cells, are three-dimensional cell cultures that recapitulate the cellular organization, transcriptional and epigenetic signatures of their counterpart organs. Recent studies have indicated their great values as experimental virology platforms, making human organoid an ideal tool for investigating host–pathogen interactions. Here, we summarize research developments for SARS-CoV-2 infection of various human organoids involved in multiple systems, including lung, liver, brain, intestine, kidney and blood vessel organoids. These studies help us reveal the pathogenesis mechanism of COVID-19, and facilitate the development of effective vaccines and drugs as well as other therapeutic regimes.
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spelling pubmed-82779872021-07-14 Defense of COVID-19 by Human Organoids Lv, Ting Meng, Fanlu Yu, Meng Huang, Haihui Lin, Xinhua Zhao, Bing Phenomics Review Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has created an immense menace to public health worldwide, exerting huge effects on global economic and political conditions. Understanding the biology and pathogenesis mechanisms of this novel virus, in large parts, relies on optimal physiological models that allow replication and propagation of SARS-CoV-2. Human organoids, derived from stem cells, are three-dimensional cell cultures that recapitulate the cellular organization, transcriptional and epigenetic signatures of their counterpart organs. Recent studies have indicated their great values as experimental virology platforms, making human organoid an ideal tool for investigating host–pathogen interactions. Here, we summarize research developments for SARS-CoV-2 infection of various human organoids involved in multiple systems, including lung, liver, brain, intestine, kidney and blood vessel organoids. These studies help us reveal the pathogenesis mechanism of COVID-19, and facilitate the development of effective vaccines and drugs as well as other therapeutic regimes. Springer Singapore 2021-07-14 /pmc/articles/PMC8277987/ /pubmed/35233559 http://dx.doi.org/10.1007/s43657-021-00015-0 Text en © International Human Phenome Institutes (Shanghai) 2021
spellingShingle Review
Lv, Ting
Meng, Fanlu
Yu, Meng
Huang, Haihui
Lin, Xinhua
Zhao, Bing
Defense of COVID-19 by Human Organoids
title Defense of COVID-19 by Human Organoids
title_full Defense of COVID-19 by Human Organoids
title_fullStr Defense of COVID-19 by Human Organoids
title_full_unstemmed Defense of COVID-19 by Human Organoids
title_short Defense of COVID-19 by Human Organoids
title_sort defense of covid-19 by human organoids
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277987/
https://www.ncbi.nlm.nih.gov/pubmed/35233559
http://dx.doi.org/10.1007/s43657-021-00015-0
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