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Generation of vascularized human cardiac organoids for 3D in vitro modeling

Here, we provide a protocol for next-generation human cardiac organoid modeling containing markers of vascularized tissues. We describe steps for cardiac differentiation, harvesting cardiac cells, and generating vascularized human cardiac organoids. We then detail downstream analysis of functional p...

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Detalles Bibliográficos
Autores principales: Voges, Holly K., Mills, Richard J., Porrello, Enzo R., Hudson, James E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511847/
https://www.ncbi.nlm.nih.gov/pubmed/37384522
http://dx.doi.org/10.1016/j.xpro.2023.102371
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author Voges, Holly K.
Mills, Richard J.
Porrello, Enzo R.
Hudson, James E.
author_facet Voges, Holly K.
Mills, Richard J.
Porrello, Enzo R.
Hudson, James E.
author_sort Voges, Holly K.
collection PubMed
description Here, we provide a protocol for next-generation human cardiac organoid modeling containing markers of vascularized tissues. We describe steps for cardiac differentiation, harvesting cardiac cells, and generating vascularized human cardiac organoids. We then detail downstream analysis of functional parameters and fluorescence labeling of human cardiac organoids. This protocol is useful for high throughput disease modeling, drug discovery, and providing mechanistic insight into cell-cell and cell-matrix interactions. For complete details on the use and execution of this protocol, please refer to Voges et al.(1) and Mills et al.(2)
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spelling pubmed-105118472023-09-22 Generation of vascularized human cardiac organoids for 3D in vitro modeling Voges, Holly K. Mills, Richard J. Porrello, Enzo R. Hudson, James E. STAR Protoc Protocol Here, we provide a protocol for next-generation human cardiac organoid modeling containing markers of vascularized tissues. We describe steps for cardiac differentiation, harvesting cardiac cells, and generating vascularized human cardiac organoids. We then detail downstream analysis of functional parameters and fluorescence labeling of human cardiac organoids. This protocol is useful for high throughput disease modeling, drug discovery, and providing mechanistic insight into cell-cell and cell-matrix interactions. For complete details on the use and execution of this protocol, please refer to Voges et al.(1) and Mills et al.(2) Elsevier 2023-06-28 /pmc/articles/PMC10511847/ /pubmed/37384522 http://dx.doi.org/10.1016/j.xpro.2023.102371 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Voges, Holly K.
Mills, Richard J.
Porrello, Enzo R.
Hudson, James E.
Generation of vascularized human cardiac organoids for 3D in vitro modeling
title Generation of vascularized human cardiac organoids for 3D in vitro modeling
title_full Generation of vascularized human cardiac organoids for 3D in vitro modeling
title_fullStr Generation of vascularized human cardiac organoids for 3D in vitro modeling
title_full_unstemmed Generation of vascularized human cardiac organoids for 3D in vitro modeling
title_short Generation of vascularized human cardiac organoids for 3D in vitro modeling
title_sort generation of vascularized human cardiac organoids for 3d in vitro modeling
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511847/
https://www.ncbi.nlm.nih.gov/pubmed/37384522
http://dx.doi.org/10.1016/j.xpro.2023.102371
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