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Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries

Acute cardiac injuries occur in 20%–25% of hospitalized COVID‐19 patients. Herein, we demonstrate that human cardiac organoids (hCOs) are a viable platform to model the cardiac injuries caused by COVID‐19 hyperinflammation. As IL‐1β is an upstream cytokine and a core COVID‐19 signature cytokine, it...

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Autores principales: Arhontoulis, Dimitrios C., Kerr, Charles M., Richards, Dylan, Tjen, Kelsey, Hyams, Nathaniel, Jones, Jefferey A., Deleon‐Pennell, Kristine, Menick, Donald, Bräuninger, Hanna, Lindner, Diana, Westermann, Dirk, Mei, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350263/
https://www.ncbi.nlm.nih.gov/pubmed/35689600
http://dx.doi.org/10.1002/term.3327
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author Arhontoulis, Dimitrios C.
Kerr, Charles M.
Richards, Dylan
Tjen, Kelsey
Hyams, Nathaniel
Jones, Jefferey A.
Deleon‐Pennell, Kristine
Menick, Donald
Bräuninger, Hanna
Lindner, Diana
Westermann, Dirk
Mei, Ying
author_facet Arhontoulis, Dimitrios C.
Kerr, Charles M.
Richards, Dylan
Tjen, Kelsey
Hyams, Nathaniel
Jones, Jefferey A.
Deleon‐Pennell, Kristine
Menick, Donald
Bräuninger, Hanna
Lindner, Diana
Westermann, Dirk
Mei, Ying
author_sort Arhontoulis, Dimitrios C.
collection PubMed
description Acute cardiac injuries occur in 20%–25% of hospitalized COVID‐19 patients. Herein, we demonstrate that human cardiac organoids (hCOs) are a viable platform to model the cardiac injuries caused by COVID‐19 hyperinflammation. As IL‐1β is an upstream cytokine and a core COVID‐19 signature cytokine, it was used to stimulate hCOs to induce the release of a milieu of proinflammatory cytokines that mirror the profile of COVID‐19 cytokine storm. The IL‐1β treated hCOs recapitulated transcriptomic, structural, and functional signatures of COVID‐19 hearts. The comparison of IL‐1β treated hCOs with cardiac tissue from COVID‐19 autopsies illustrated the critical roles of hyper‐inflammation in COVID‐19 cardiac insults and indicated the cardioprotective effects of endothelium. The IL‐1β treated hCOs thus provide a defined and robust model to assess the efficacy and potential side effects of immunomodulatory drugs, as well as the reversibility of COVID‐19 cardiac injuries at baseline and simulated exercise conditions.
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spelling pubmed-93502632022-08-04 Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries Arhontoulis, Dimitrios C. Kerr, Charles M. Richards, Dylan Tjen, Kelsey Hyams, Nathaniel Jones, Jefferey A. Deleon‐Pennell, Kristine Menick, Donald Bräuninger, Hanna Lindner, Diana Westermann, Dirk Mei, Ying J Tissue Eng Regen Med Research Articles Acute cardiac injuries occur in 20%–25% of hospitalized COVID‐19 patients. Herein, we demonstrate that human cardiac organoids (hCOs) are a viable platform to model the cardiac injuries caused by COVID‐19 hyperinflammation. As IL‐1β is an upstream cytokine and a core COVID‐19 signature cytokine, it was used to stimulate hCOs to induce the release of a milieu of proinflammatory cytokines that mirror the profile of COVID‐19 cytokine storm. The IL‐1β treated hCOs recapitulated transcriptomic, structural, and functional signatures of COVID‐19 hearts. The comparison of IL‐1β treated hCOs with cardiac tissue from COVID‐19 autopsies illustrated the critical roles of hyper‐inflammation in COVID‐19 cardiac insults and indicated the cardioprotective effects of endothelium. The IL‐1β treated hCOs thus provide a defined and robust model to assess the efficacy and potential side effects of immunomodulatory drugs, as well as the reversibility of COVID‐19 cardiac injuries at baseline and simulated exercise conditions. John Wiley and Sons Inc. 2022-06-11 2022-09 /pmc/articles/PMC9350263/ /pubmed/35689600 http://dx.doi.org/10.1002/term.3327 Text en © 2022 The Authors. Journal of Tissue Engineering and Regenerative Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Arhontoulis, Dimitrios C.
Kerr, Charles M.
Richards, Dylan
Tjen, Kelsey
Hyams, Nathaniel
Jones, Jefferey A.
Deleon‐Pennell, Kristine
Menick, Donald
Bräuninger, Hanna
Lindner, Diana
Westermann, Dirk
Mei, Ying
Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries
title Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries
title_full Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries
title_fullStr Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries
title_full_unstemmed Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries
title_short Human cardiac organoids to model COVID‐19 cytokine storm induced cardiac injuries
title_sort human cardiac organoids to model covid‐19 cytokine storm induced cardiac injuries
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350263/
https://www.ncbi.nlm.nih.gov/pubmed/35689600
http://dx.doi.org/10.1002/term.3327
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