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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Main Authors: Nanako Kawaguchi, Emiko Hayama, Yoshiyuki Furutani, Toshio Nakanishi
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2012/439219
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spelling doaj-87cc5400ccad402e95f07e01e2f451f02020-11-24T21:00:24ZengHindawi LimitedStem Cells International1687-966X1687-96782012-01-01201210.1155/2012/439219439219Prospective In Vitro Models of Channelopathies and CardiomyopathiesNanako Kawaguchi0Emiko Hayama1Yoshiyuki Furutani2Toshio Nakanishi3Department of Pediatric Cardiology, Tokyo Women’s Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanDepartment of Pediatric Cardiology, Tokyo Women’s Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanDepartment of Pediatric Cardiology, Tokyo Women’s Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanDepartment of Pediatric Cardiology, Tokyo Women’s Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanAn 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.http://dx.doi.org/10.1155/2012/439219
collection DOAJ
language English
format Article
sources DOAJ
author Nanako Kawaguchi
Emiko Hayama
Yoshiyuki Furutani
Toshio Nakanishi
spellingShingle Nanako Kawaguchi
Emiko Hayama
Yoshiyuki Furutani
Toshio Nakanishi
Prospective In Vitro Models of Channelopathies and Cardiomyopathies
Stem Cells International
author_facet Nanako Kawaguchi
Emiko Hayama
Yoshiyuki Furutani
Toshio Nakanishi
author_sort Nanako Kawaguchi
title Prospective In Vitro Models of Channelopathies and Cardiomyopathies
title_short 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_sort prospective in vitro models of channelopathies and cardiomyopathies
publisher Hindawi Limited
series Stem Cells International
issn 1687-966X
1687-9678
publishDate 2012-01-01
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.
url http://dx.doi.org/10.1155/2012/439219
work_keys_str_mv AT nanakokawaguchi prospectiveinvitromodelsofchannelopathiesandcardiomyopathies
AT emikohayama prospectiveinvitromodelsofchannelopathiesandcardiomyopathies
AT yoshiyukifurutani prospectiveinvitromodelsofchannelopathiesandcardiomyopathies
AT toshionakanishi prospectiveinvitromodelsofchannelopathiesandcardiomyopathies
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