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Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19
SARS-CoV-2, the virus underlying COVID-19, has now been recognized to cause multiorgan disease with a systemic effect on the host. To effectively combat SARS-CoV-2 and the subsequent development of COVID-19, it is critical to detect, monitor, and model viral pathogenesis. In this review, we discuss...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171291/ https://www.ncbi.nlm.nih.gov/pubmed/37167356 http://dx.doi.org/10.1161/CIRCRESAHA.122.321877 |
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author | Satta, Sandro Rockwood, Sarah J. Wang, Kaidong Wang, Shaolei Mozneb, Maedeh Arzt, Madelyn Hsiai, Tzung K. Sharma, Arun |
author_facet | Satta, Sandro Rockwood, Sarah J. Wang, Kaidong Wang, Shaolei Mozneb, Maedeh Arzt, Madelyn Hsiai, Tzung K. Sharma, Arun |
author_sort | Satta, Sandro |
collection | PubMed |
description | SARS-CoV-2, the virus underlying COVID-19, has now been recognized to cause multiorgan disease with a systemic effect on the host. To effectively combat SARS-CoV-2 and the subsequent development of COVID-19, it is critical to detect, monitor, and model viral pathogenesis. In this review, we discuss recent advancements in microfluidics, organ-on-a-chip, and human stem cell–derived models to study SARS-CoV-2 infection in the physiological organ microenvironment, together with their limitations. Microfluidic-based detection methods have greatly enhanced the rapidity, accessibility, and sensitivity of viral detection from patient samples. Engineered organ-on-a-chip models that recapitulate in vivo physiology have been developed for many organ systems to study viral pathology. Human stem cell–derived models have been utilized not only to model viral tropism and pathogenesis in a physiologically relevant context but also to screen for effective therapeutic compounds. The combination of all these platforms, along with future advancements, may aid to identify potential targets and develop novel strategies to counteract COVID-19 pathogenesis. |
format | Online Article Text |
id | pubmed-10171291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-101712912023-05-12 Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 Satta, Sandro Rockwood, Sarah J. Wang, Kaidong Wang, Shaolei Mozneb, Maedeh Arzt, Madelyn Hsiai, Tzung K. Sharma, Arun Circ Res Compendium on COVID-19 and Cardiovascular Disease SARS-CoV-2, the virus underlying COVID-19, has now been recognized to cause multiorgan disease with a systemic effect on the host. To effectively combat SARS-CoV-2 and the subsequent development of COVID-19, it is critical to detect, monitor, and model viral pathogenesis. In this review, we discuss recent advancements in microfluidics, organ-on-a-chip, and human stem cell–derived models to study SARS-CoV-2 infection in the physiological organ microenvironment, together with their limitations. Microfluidic-based detection methods have greatly enhanced the rapidity, accessibility, and sensitivity of viral detection from patient samples. Engineered organ-on-a-chip models that recapitulate in vivo physiology have been developed for many organ systems to study viral pathology. Human stem cell–derived models have been utilized not only to model viral tropism and pathogenesis in a physiologically relevant context but also to screen for effective therapeutic compounds. The combination of all these platforms, along with future advancements, may aid to identify potential targets and develop novel strategies to counteract COVID-19 pathogenesis. Lippincott Williams & Wilkins 2023-05-12 2023-05-12 /pmc/articles/PMC10171291/ /pubmed/37167356 http://dx.doi.org/10.1161/CIRCRESAHA.122.321877 Text en © 2023 American Heart Association, Inc. This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections. |
spellingShingle | Compendium on COVID-19 and Cardiovascular Disease Satta, Sandro Rockwood, Sarah J. Wang, Kaidong Wang, Shaolei Mozneb, Maedeh Arzt, Madelyn Hsiai, Tzung K. Sharma, Arun Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 |
title | Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 |
title_full | Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 |
title_fullStr | Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 |
title_full_unstemmed | Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 |
title_short | Microfluidic Organ-Chips and Stem Cell Models in the Fight Against COVID-19 |
title_sort | microfluidic organ-chips and stem cell models in the fight against covid-19 |
topic | Compendium on COVID-19 and Cardiovascular Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171291/ https://www.ncbi.nlm.nih.gov/pubmed/37167356 http://dx.doi.org/10.1161/CIRCRESAHA.122.321877 |
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