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Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future

Cardiovascular disease (CVD), despite the advances of the medical field, remains one of the leading causes of mortality worldwide. Discovering novel treatments based on cell therapy or drugs is critical, and induced pluripotent stem cells (iPS Cells) technology has made it possible to design extensi...

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Autores principales: Tsifaki, Marianna, Kelaini, Sophia, Caines, Rachel, Yang, Chunbo, Margariti, Andriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109758/
https://www.ncbi.nlm.nih.gov/pubmed/30177971
http://dx.doi.org/10.3389/fcvm.2018.00109
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author Tsifaki, Marianna
Kelaini, Sophia
Caines, Rachel
Yang, Chunbo
Margariti, Andriana
author_facet Tsifaki, Marianna
Kelaini, Sophia
Caines, Rachel
Yang, Chunbo
Margariti, Andriana
author_sort Tsifaki, Marianna
collection PubMed
description Cardiovascular disease (CVD), despite the advances of the medical field, remains one of the leading causes of mortality worldwide. Discovering novel treatments based on cell therapy or drugs is critical, and induced pluripotent stem cells (iPS Cells) technology has made it possible to design extensive disease-specific in vitro models. Elucidating the differentiation process challenged our previous knowledge of cell plasticity and capabilities and allows the concept of cell reprogramming technology to be established, which has inspired the creation of both in vitro and in vivo techniques. Patient-specific cell lines provide the opportunity of studying their pathophysiology in vitro, which can lead to novel drug development. At the same time, in vivo models have been designed where in situ transdifferentiation of cell populations into cardiomyocytes or endothelial cells (ECs) give hope toward effective cell therapies. Unfortunately, the efficiency as well as the concerns about the safety of all these methods make it exceedingly difficult to pass to the clinical trial phase. It is our opinion that creating an ex vivo model out of patient-specific cells will be one of the most important goals in the future to help surpass all these hindrances. Thus, in this review we aim to present the current state of research in reprogramming toward the cardiovascular system's regeneration, and showcase how the development and study of a multicellular 3D ex vivo model will improve our fighting chances.
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spelling pubmed-61097582018-09-03 Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future Tsifaki, Marianna Kelaini, Sophia Caines, Rachel Yang, Chunbo Margariti, Andriana Front Cardiovasc Med Cardiovascular Medicine Cardiovascular disease (CVD), despite the advances of the medical field, remains one of the leading causes of mortality worldwide. Discovering novel treatments based on cell therapy or drugs is critical, and induced pluripotent stem cells (iPS Cells) technology has made it possible to design extensive disease-specific in vitro models. Elucidating the differentiation process challenged our previous knowledge of cell plasticity and capabilities and allows the concept of cell reprogramming technology to be established, which has inspired the creation of both in vitro and in vivo techniques. Patient-specific cell lines provide the opportunity of studying their pathophysiology in vitro, which can lead to novel drug development. At the same time, in vivo models have been designed where in situ transdifferentiation of cell populations into cardiomyocytes or endothelial cells (ECs) give hope toward effective cell therapies. Unfortunately, the efficiency as well as the concerns about the safety of all these methods make it exceedingly difficult to pass to the clinical trial phase. It is our opinion that creating an ex vivo model out of patient-specific cells will be one of the most important goals in the future to help surpass all these hindrances. Thus, in this review we aim to present the current state of research in reprogramming toward the cardiovascular system's regeneration, and showcase how the development and study of a multicellular 3D ex vivo model will improve our fighting chances. Frontiers Media S.A. 2018-08-20 /pmc/articles/PMC6109758/ /pubmed/30177971 http://dx.doi.org/10.3389/fcvm.2018.00109 Text en Copyright © 2018 Tsifaki, Kelaini, Caines, Yang and Margariti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Tsifaki, Marianna
Kelaini, Sophia
Caines, Rachel
Yang, Chunbo
Margariti, Andriana
Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future
title Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future
title_full Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future
title_fullStr Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future
title_full_unstemmed Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future
title_short Regenerating the Cardiovascular System Through Cell Reprogramming; Current Approaches and a Look Into the Future
title_sort regenerating the cardiovascular system through cell reprogramming; current approaches and a look into the future
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109758/
https://www.ncbi.nlm.nih.gov/pubmed/30177971
http://dx.doi.org/10.3389/fcvm.2018.00109
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