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Isolation, culture, and immunostaining of neonatal rat ventricular myocytes

Isolation and culture of ventricular cardiomyocytes from neonatal rats (NRVMs) is a powerful model to study neonatal cardiac development, cell cycle regulation, and cardiac physiology and pathology in vitro. Here, we present our modified enzymatic digestion protocol followed by two-step discontinuou...

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Detalles Bibliográficos
Autores principales: Pereira, Ana Helena Macedo, Cardoso, Alisson Campos, Franchini, Kleber Gomes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599495/
https://www.ncbi.nlm.nih.gov/pubmed/34820638
http://dx.doi.org/10.1016/j.xpro.2021.100950
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author Pereira, Ana Helena Macedo
Cardoso, Alisson Campos
Franchini, Kleber Gomes
author_facet Pereira, Ana Helena Macedo
Cardoso, Alisson Campos
Franchini, Kleber Gomes
author_sort Pereira, Ana Helena Macedo
collection PubMed
description Isolation and culture of ventricular cardiomyocytes from neonatal rats (NRVMs) is a powerful model to study neonatal cardiac development, cell cycle regulation, and cardiac physiology and pathology in vitro. Here, we present our modified enzymatic digestion protocol followed by two-step discontinuous Percoll gradient centrifugation to isolate a high yield of viable ventricular cardiomyocytes from neonatal rats. Finally, here we describe an immunostaining protocol for cytosolic and nuclear staining of NRVMs. For complete details on the use and execution of this protocol, please refer to Pereira et al. (2020).
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spelling pubmed-85994952021-11-23 Isolation, culture, and immunostaining of neonatal rat ventricular myocytes Pereira, Ana Helena Macedo Cardoso, Alisson Campos Franchini, Kleber Gomes STAR Protoc Protocol Isolation and culture of ventricular cardiomyocytes from neonatal rats (NRVMs) is a powerful model to study neonatal cardiac development, cell cycle regulation, and cardiac physiology and pathology in vitro. Here, we present our modified enzymatic digestion protocol followed by two-step discontinuous Percoll gradient centrifugation to isolate a high yield of viable ventricular cardiomyocytes from neonatal rats. Finally, here we describe an immunostaining protocol for cytosolic and nuclear staining of NRVMs. For complete details on the use and execution of this protocol, please refer to Pereira et al. (2020). Elsevier 2021-11-12 /pmc/articles/PMC8599495/ /pubmed/34820638 http://dx.doi.org/10.1016/j.xpro.2021.100950 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Pereira, Ana Helena Macedo
Cardoso, Alisson Campos
Franchini, Kleber Gomes
Isolation, culture, and immunostaining of neonatal rat ventricular myocytes
title Isolation, culture, and immunostaining of neonatal rat ventricular myocytes
title_full Isolation, culture, and immunostaining of neonatal rat ventricular myocytes
title_fullStr Isolation, culture, and immunostaining of neonatal rat ventricular myocytes
title_full_unstemmed Isolation, culture, and immunostaining of neonatal rat ventricular myocytes
title_short Isolation, culture, and immunostaining of neonatal rat ventricular myocytes
title_sort isolation, culture, and immunostaining of neonatal rat ventricular myocytes
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599495/
https://www.ncbi.nlm.nih.gov/pubmed/34820638
http://dx.doi.org/10.1016/j.xpro.2021.100950
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