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Heart regeneration using reprogramming technology

Loss of terminally differentiated cardiomyocytes due to heart disease is irreversible and current therapeutic regimes are limited. Cell therapy using stem cell-derived cardiomyocytes is an attractive option to repair injured hearts. The discovery of direct reprogramming of fibroblasts into induced p...

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Detalles Bibliográficos
Autor principal: IEDA, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647079/
https://www.ncbi.nlm.nih.gov/pubmed/23474887
http://dx.doi.org/10.2183/pjab.89.118
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author IEDA, Masaki
author_facet IEDA, Masaki
author_sort IEDA, Masaki
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description Loss of terminally differentiated cardiomyocytes due to heart disease is irreversible and current therapeutic regimes are limited. Cell therapy using stem cell-derived cardiomyocytes is an attractive option to repair injured hearts. The discovery of direct reprogramming of fibroblasts into induced pluripotent stem cells (iPSCs) and successful differentiation of iPSCs into cardiomyocytes provided a revolutionary paradigm in heart regenerative research. During the past decades, significant advances in stem cell culture, differentiation and purification protocols, as well as in cell transplantation methodologies, have been achieved. On the other hand, recent studies demonstrated that a somatic cell could be converted into an alternative differentiated cell type without first becoming a stem cell by overexpression of lineage-specific factors. We found that functional cardiomyocytes can be directly induced from fibroblasts by a combination of three cardiac transcription factors, Gata4, Mef2c and Tbx5, in vitro and in vivo. I will review the perspectives of heart regeneration using reprogramming technology.
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spelling pubmed-36470792013-05-20 Heart regeneration using reprogramming technology IEDA, Masaki Proc Jpn Acad Ser B Phys Biol Sci Review Loss of terminally differentiated cardiomyocytes due to heart disease is irreversible and current therapeutic regimes are limited. Cell therapy using stem cell-derived cardiomyocytes is an attractive option to repair injured hearts. The discovery of direct reprogramming of fibroblasts into induced pluripotent stem cells (iPSCs) and successful differentiation of iPSCs into cardiomyocytes provided a revolutionary paradigm in heart regenerative research. During the past decades, significant advances in stem cell culture, differentiation and purification protocols, as well as in cell transplantation methodologies, have been achieved. On the other hand, recent studies demonstrated that a somatic cell could be converted into an alternative differentiated cell type without first becoming a stem cell by overexpression of lineage-specific factors. We found that functional cardiomyocytes can be directly induced from fibroblasts by a combination of three cardiac transcription factors, Gata4, Mef2c and Tbx5, in vitro and in vivo. I will review the perspectives of heart regeneration using reprogramming technology. The Japan Academy 2013-03-11 /pmc/articles/PMC3647079/ /pubmed/23474887 http://dx.doi.org/10.2183/pjab.89.118 Text en © 2013 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
IEDA, Masaki
Heart regeneration using reprogramming technology
title Heart regeneration using reprogramming technology
title_full Heart regeneration using reprogramming technology
title_fullStr Heart regeneration using reprogramming technology
title_full_unstemmed Heart regeneration using reprogramming technology
title_short Heart regeneration using reprogramming technology
title_sort heart regeneration using reprogramming technology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647079/
https://www.ncbi.nlm.nih.gov/pubmed/23474887
http://dx.doi.org/10.2183/pjab.89.118
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