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Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix
The increased knowledge in cell signals and stem cell differentiation, together with the development of new technologies, such as 3D bioprinting, has made the generation of artificial tissues more feasible for in vitro studies and in vivo applications. In the human body, cell fate, function, and sur...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500153/ https://www.ncbi.nlm.nih.gov/pubmed/33015056 http://dx.doi.org/10.3389/fcell.2020.559032 |
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author | Pagliarosi, Olivia Picchio, Vittorio Chimenti, Isotta Messina, Elisa Gaetani, Roberto |
author_facet | Pagliarosi, Olivia Picchio, Vittorio Chimenti, Isotta Messina, Elisa Gaetani, Roberto |
author_sort | Pagliarosi, Olivia |
collection | PubMed |
description | The increased knowledge in cell signals and stem cell differentiation, together with the development of new technologies, such as 3D bioprinting, has made the generation of artificial tissues more feasible for in vitro studies and in vivo applications. In the human body, cell fate, function, and survival are determined by the microenvironment, a rich and complex network composed of extracellular matrix (ECM), different cell types, and soluble factors. They all interconnect and communicate, receiving and sending signals, modulating and responding to cues. In the cardiovascular field, the culture of stem cells in vitro and their differentiation into cardiac phenotypes is well established, although differentiated cardiomyocytes often lack the functional maturation and structural organization typical of the adult myocardium. The recreation of an artificial microenvironment as similar as possible to the native tissue, though, has been shown to partly overcome these limitations, and can be obtained through the proper combination of ECM molecules, different cell types, bioavailability of growth factors (GFs), as well as appropriate mechanical and geometrical stimuli. This review will focus on the role of the ECM in the regulation of cardiac differentiation, will provide new insights on the role of supporting cells in the generation of 3D artificial tissues, and will also present a selection of the latest approaches to recreate a cardiac microenvironment in vitro through 3D bioprinting approaches. |
format | Online Article Text |
id | pubmed-7500153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75001532020-10-02 Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix Pagliarosi, Olivia Picchio, Vittorio Chimenti, Isotta Messina, Elisa Gaetani, Roberto Front Cell Dev Biol Cell and Developmental Biology The increased knowledge in cell signals and stem cell differentiation, together with the development of new technologies, such as 3D bioprinting, has made the generation of artificial tissues more feasible for in vitro studies and in vivo applications. In the human body, cell fate, function, and survival are determined by the microenvironment, a rich and complex network composed of extracellular matrix (ECM), different cell types, and soluble factors. They all interconnect and communicate, receiving and sending signals, modulating and responding to cues. In the cardiovascular field, the culture of stem cells in vitro and their differentiation into cardiac phenotypes is well established, although differentiated cardiomyocytes often lack the functional maturation and structural organization typical of the adult myocardium. The recreation of an artificial microenvironment as similar as possible to the native tissue, though, has been shown to partly overcome these limitations, and can be obtained through the proper combination of ECM molecules, different cell types, bioavailability of growth factors (GFs), as well as appropriate mechanical and geometrical stimuli. This review will focus on the role of the ECM in the regulation of cardiac differentiation, will provide new insights on the role of supporting cells in the generation of 3D artificial tissues, and will also present a selection of the latest approaches to recreate a cardiac microenvironment in vitro through 3D bioprinting approaches. Frontiers Media S.A. 2020-09-04 /pmc/articles/PMC7500153/ /pubmed/33015056 http://dx.doi.org/10.3389/fcell.2020.559032 Text en Copyright © 2020 Pagliarosi, Picchio, Chimenti, Messina and Gaetani. 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 | Cell and Developmental Biology Pagliarosi, Olivia Picchio, Vittorio Chimenti, Isotta Messina, Elisa Gaetani, Roberto Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix |
title | Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix |
title_full | Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix |
title_fullStr | Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix |
title_full_unstemmed | Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix |
title_short | Building an Artificial Cardiac Microenvironment: A Focus on the Extracellular Matrix |
title_sort | building an artificial cardiac microenvironment: a focus on the extracellular matrix |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500153/ https://www.ncbi.nlm.nih.gov/pubmed/33015056 http://dx.doi.org/10.3389/fcell.2020.559032 |
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