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Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart
Myocardial infarction is one of the leading causes of death worldwide. Bone marrow contains different types of stem cells capable of differentiating into cardiomyocytes. Therefore, we hypothesized that bone marrow contains a lin-c-kit+ progenitor cell pool with the ability to home to the infarcted r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Journal of Stem cells and Regenerative medicine
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908253/ https://www.ncbi.nlm.nih.gov/pubmed/24693056 |
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author | Khan, M Mohsin, S Khan, SN Riazuddin, S |
author_facet | Khan, M Mohsin, S Khan, SN Riazuddin, S |
author_sort | Khan, M |
collection | PubMed |
description | Myocardial infarction is one of the leading causes of death worldwide. Bone marrow contains different types of stem cells capable of differentiating into cardiomyocytes. Therefore, we hypothesized that bone marrow contains a lin-c-kit+ progenitor cell pool with the ability to home to the infarcted region and improve the cardiac function. BM-derived stem cells (BMSCs) from Green fluorescent protein (GFP) expressing transgenic mice C57BL/6 (n = 6) were isolated by c-kit labeled Microbeads. Lin-c-kit+ BMSCs co-cultured with rat neonatal cardiomyocytes were able to express cardiac marker and form intercellular connections with rat myocytes. Myocardial infarction was produced in the experimental animals C57BL/6 Wild type (n = 10) by permanent ligation of the Left anterior descending (LAD) artery. BMSCs enriched for c-kit were transplanted in the border zone area of the infarction. Cardiac function analyzed by Millar’s Apparatus after 4 weeks of transplantation showed improvement. BMSCs were able to form intercellular connections and new blood vessel formation as determined by Connexin 43 and CD31 respectively. Lin-c-kit(+) BMSCs were able to align with the host myocardium, participate in angiogenesis and thus improve the cardiac function. |
format | Online Article Text |
id | pubmed-3908253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Journal of Stem cells and Regenerative medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-39082532014-04-01 Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart Khan, M Mohsin, S Khan, SN Riazuddin, S J Stem Cells Regen Med Original Article Myocardial infarction is one of the leading causes of death worldwide. Bone marrow contains different types of stem cells capable of differentiating into cardiomyocytes. Therefore, we hypothesized that bone marrow contains a lin-c-kit+ progenitor cell pool with the ability to home to the infarcted region and improve the cardiac function. BM-derived stem cells (BMSCs) from Green fluorescent protein (GFP) expressing transgenic mice C57BL/6 (n = 6) were isolated by c-kit labeled Microbeads. Lin-c-kit+ BMSCs co-cultured with rat neonatal cardiomyocytes were able to express cardiac marker and form intercellular connections with rat myocytes. Myocardial infarction was produced in the experimental animals C57BL/6 Wild type (n = 10) by permanent ligation of the Left anterior descending (LAD) artery. BMSCs enriched for c-kit were transplanted in the border zone area of the infarction. Cardiac function analyzed by Millar’s Apparatus after 4 weeks of transplantation showed improvement. BMSCs were able to form intercellular connections and new blood vessel formation as determined by Connexin 43 and CD31 respectively. Lin-c-kit(+) BMSCs were able to align with the host myocardium, participate in angiogenesis and thus improve the cardiac function. Journal of Stem cells and Regenerative medicine 2010-04-05 /pmc/articles/PMC3908253/ /pubmed/24693056 Text en Copyright © 2010 Journal of Stem cells and Regenerative medicine http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Khan, M Mohsin, S Khan, SN Riazuddin, S Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart |
title | Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart |
title_full | Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart |
title_fullStr | Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart |
title_full_unstemmed | Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart |
title_short | Lin-c-kit(+) BM-derived stem cells repair Infarcted Heart |
title_sort | lin-c-kit(+) bm-derived stem cells repair infarcted heart |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3908253/ https://www.ncbi.nlm.nih.gov/pubmed/24693056 |
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