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Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis

The possibility to employ stem/progenitor cells in the cardiovascular remodelling after myocardial infarction is one of the main queries of regenerative medicine. To investigate whether endothelial progenitor cells (EPCs) participate in the restoration of hypoxia‐affected myocardium, we used a co‐cu...

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Autores principales: Rosca, Ana‐Maria, Mitroi, Daniel Nicolae, Cismasiu, Valeriu, Badea, Rodica, Necula‐Petrareanu, Georgiana, Preda, Mihai Bogdan, Niculite, Cristina, Tutuianu, Raluca, Szedlacsek, Stefan, Burlacu, Alexandrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156385/
https://www.ncbi.nlm.nih.gov/pubmed/30044046
http://dx.doi.org/10.1111/jcmm.13712
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author Rosca, Ana‐Maria
Mitroi, Daniel Nicolae
Cismasiu, Valeriu
Badea, Rodica
Necula‐Petrareanu, Georgiana
Preda, Mihai Bogdan
Niculite, Cristina
Tutuianu, Raluca
Szedlacsek, Stefan
Burlacu, Alexandrina
author_facet Rosca, Ana‐Maria
Mitroi, Daniel Nicolae
Cismasiu, Valeriu
Badea, Rodica
Necula‐Petrareanu, Georgiana
Preda, Mihai Bogdan
Niculite, Cristina
Tutuianu, Raluca
Szedlacsek, Stefan
Burlacu, Alexandrina
author_sort Rosca, Ana‐Maria
collection PubMed
description The possibility to employ stem/progenitor cells in the cardiovascular remodelling after myocardial infarction is one of the main queries of regenerative medicine. To investigate whether endothelial progenitor cells (EPCs) participate in the restoration of hypoxia‐affected myocardium, we used a co‐culture model that allowed the intimate interaction between EPCs and myocardial slices, mimicking stem cell transplantation into the ischaemic heart. On this model, we showed that EPCs engrafted to some extent and only transiently survived into the host tissue, yet produced visible protective effects, in terms of angiogenesis and protection against apoptosis and identified miR‐377‐VE‐PTP axis as being involved in the protective effects of EPCs in hypoxic myocardium. We also showed that collagen, the main component of the myocardial scar, was important for these protective effects by preserving VE‐PTP levels, which were otherwise diminished by miR‐377. By this, a good face of the scar is revealed, which was so far perceived as having only detrimental impact on the exogenously delivered stem/progenitor cells by affecting not only the engraftment, but also the general protective effects of stem cells.
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spelling pubmed-61563852018-10-01 Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis Rosca, Ana‐Maria Mitroi, Daniel Nicolae Cismasiu, Valeriu Badea, Rodica Necula‐Petrareanu, Georgiana Preda, Mihai Bogdan Niculite, Cristina Tutuianu, Raluca Szedlacsek, Stefan Burlacu, Alexandrina J Cell Mol Med Original Articles The possibility to employ stem/progenitor cells in the cardiovascular remodelling after myocardial infarction is one of the main queries of regenerative medicine. To investigate whether endothelial progenitor cells (EPCs) participate in the restoration of hypoxia‐affected myocardium, we used a co‐culture model that allowed the intimate interaction between EPCs and myocardial slices, mimicking stem cell transplantation into the ischaemic heart. On this model, we showed that EPCs engrafted to some extent and only transiently survived into the host tissue, yet produced visible protective effects, in terms of angiogenesis and protection against apoptosis and identified miR‐377‐VE‐PTP axis as being involved in the protective effects of EPCs in hypoxic myocardium. We also showed that collagen, the main component of the myocardial scar, was important for these protective effects by preserving VE‐PTP levels, which were otherwise diminished by miR‐377. By this, a good face of the scar is revealed, which was so far perceived as having only detrimental impact on the exogenously delivered stem/progenitor cells by affecting not only the engraftment, but also the general protective effects of stem cells. John Wiley and Sons Inc. 2018-07-25 2018-10 /pmc/articles/PMC6156385/ /pubmed/30044046 http://dx.doi.org/10.1111/jcmm.13712 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rosca, Ana‐Maria
Mitroi, Daniel Nicolae
Cismasiu, Valeriu
Badea, Rodica
Necula‐Petrareanu, Georgiana
Preda, Mihai Bogdan
Niculite, Cristina
Tutuianu, Raluca
Szedlacsek, Stefan
Burlacu, Alexandrina
Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis
title Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis
title_full Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis
title_fullStr Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis
title_full_unstemmed Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis
title_short Collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving miR‐377/VE‐PTP axis
title_sort collagen regulates the ability of endothelial progenitor cells to protect hypoxic myocardium through a mechanism involving mir‐377/ve‐ptp axis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156385/
https://www.ncbi.nlm.nih.gov/pubmed/30044046
http://dx.doi.org/10.1111/jcmm.13712
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