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Prospective In Vitro Models of Channelopathies and Cardiomyopathies

An in vitro heart disease model is a promising model used for identifying the genes responsible for the disease, evaluating the effects of drugs, and regenerative medicine. We were interested in disease models using a patient-induced pluripotent stem (iPS) cell-derived cardiomyocytes because of thei...

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Detalles Bibliográficos
Autores principales: Kawaguchi, Nanako, Hayama, Emiko, Furutani, Yoshiyuki, Nakanishi, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437306/
https://www.ncbi.nlm.nih.gov/pubmed/22969812
http://dx.doi.org/10.1155/2012/439219
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author Kawaguchi, Nanako
Hayama, Emiko
Furutani, Yoshiyuki
Nakanishi, Toshio
author_facet Kawaguchi, Nanako
Hayama, Emiko
Furutani, Yoshiyuki
Nakanishi, Toshio
author_sort Kawaguchi, Nanako
collection PubMed
description An in vitro heart disease model is a promising model used for identifying the genes responsible for the disease, evaluating the effects of drugs, and regenerative medicine. We were interested in disease models using a patient-induced pluripotent stem (iPS) cell-derived cardiomyocytes because of their similarity to a patient's tissues. However, as these studies have just begun, we would like to review the literature in this and other related fields and discuss the path for future models of molecular biology that can help to diagnose and cure diseases, and its involvement in regenerative medicine. The heterogeneity of iPS cells and/or differentiated cardiomyocytes has been recognized as a problem. An in vitro heart disease model should be evaluated using molecular biological analyses, such as mRNA and micro-RNA expression profiles and proteomic analysis.
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spelling pubmed-34373062012-09-11 Prospective In Vitro Models of Channelopathies and Cardiomyopathies Kawaguchi, Nanako Hayama, Emiko Furutani, Yoshiyuki Nakanishi, Toshio Stem Cells Int Review Article An in vitro heart disease model is a promising model used for identifying the genes responsible for the disease, evaluating the effects of drugs, and regenerative medicine. We were interested in disease models using a patient-induced pluripotent stem (iPS) cell-derived cardiomyocytes because of their similarity to a patient's tissues. However, as these studies have just begun, we would like to review the literature in this and other related fields and discuss the path for future models of molecular biology that can help to diagnose and cure diseases, and its involvement in regenerative medicine. The heterogeneity of iPS cells and/or differentiated cardiomyocytes has been recognized as a problem. An in vitro heart disease model should be evaluated using molecular biological analyses, such as mRNA and micro-RNA expression profiles and proteomic analysis. Hindawi Publishing Corporation 2012 2012-03-27 /pmc/articles/PMC3437306/ /pubmed/22969812 http://dx.doi.org/10.1155/2012/439219 Text en Copyright © 2012 Nanako Kawaguchi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kawaguchi, Nanako
Hayama, Emiko
Furutani, Yoshiyuki
Nakanishi, Toshio
Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title_full Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title_fullStr Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title_full_unstemmed Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title_short Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title_sort prospective in vitro models of channelopathies and cardiomyopathies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437306/
https://www.ncbi.nlm.nih.gov/pubmed/22969812
http://dx.doi.org/10.1155/2012/439219
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