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Cardiovascular regeneration
Heart disease remains the number one cause of death in developed countries. Loss of cardiomyocytes (CMs) due to aging or pathophysiological conditions (for example, myocardial infarction) is generally considered irreversible, and can lead to lethal conditions from cardiac arrhythmias to heart failur...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272765/ https://www.ncbi.nlm.nih.gov/pubmed/25689157 http://dx.doi.org/10.1186/scrt531 |
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author | Li, Ronald A |
author_facet | Li, Ronald A |
author_sort | Li, Ronald A |
collection | PubMed |
description | Heart disease remains the number one cause of death in developed countries. Loss of cardiomyocytes (CMs) due to aging or pathophysiological conditions (for example, myocardial infarction) is generally considered irreversible, and can lead to lethal conditions from cardiac arrhythmias to heart failure. Human pluripotent stem cells (PSCs), including embryonic stem cells and induced pluripotent stem cells (iPSCs), can self-renew while maintaining their pluripotency to differentiate into all cell types, including CMs. As such, PSCs represent an unprecedented unlimited ex vivo cell source. In the present thematic series, we have solicited seven review articles to discuss the current state-of-the-art PSC-based approaches for such applications as disease modeling, discovery of novel drugs and therapeutics, cardiotoxicity screening and cell-based myocardial repair, as well as the associated hurdles and potential solutions. |
format | Online Article Text |
id | pubmed-4272765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42727652014-12-22 Cardiovascular regeneration Li, Ronald A Stem Cell Res Ther Editorial Heart disease remains the number one cause of death in developed countries. Loss of cardiomyocytes (CMs) due to aging or pathophysiological conditions (for example, myocardial infarction) is generally considered irreversible, and can lead to lethal conditions from cardiac arrhythmias to heart failure. Human pluripotent stem cells (PSCs), including embryonic stem cells and induced pluripotent stem cells (iPSCs), can self-renew while maintaining their pluripotency to differentiate into all cell types, including CMs. As such, PSCs represent an unprecedented unlimited ex vivo cell source. In the present thematic series, we have solicited seven review articles to discuss the current state-of-the-art PSC-based approaches for such applications as disease modeling, discovery of novel drugs and therapeutics, cardiotoxicity screening and cell-based myocardial repair, as well as the associated hurdles and potential solutions. BioMed Central 2014-12-17 /pmc/articles/PMC4272765/ /pubmed/25689157 http://dx.doi.org/10.1186/scrt531 Text en © Li; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Editorial Li, Ronald A Cardiovascular regeneration |
title | Cardiovascular regeneration |
title_full | Cardiovascular regeneration |
title_fullStr | Cardiovascular regeneration |
title_full_unstemmed | Cardiovascular regeneration |
title_short | Cardiovascular regeneration |
title_sort | cardiovascular regeneration |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4272765/ https://www.ncbi.nlm.nih.gov/pubmed/25689157 http://dx.doi.org/10.1186/scrt531 |
work_keys_str_mv | AT lironalda cardiovascularregeneration |