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Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison
Tissue-engineered constructs are promising to overcome shortage of organ donors and to reconstruct at least parts of injured or diseased tissues or organs. However, oxygen and nutrient supply are limiting factors in many tissues, especially after implantation into the host. Therefore, the developmen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619361/ https://www.ncbi.nlm.nih.gov/pubmed/26500761 http://dx.doi.org/10.1186/s13619-015-0025-8 |
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author | Pill, Karoline Hofmann, Sandra Redl, Heinz Holnthoner, Wolfgang |
author_facet | Pill, Karoline Hofmann, Sandra Redl, Heinz Holnthoner, Wolfgang |
author_sort | Pill, Karoline |
collection | PubMed |
description | Tissue-engineered constructs are promising to overcome shortage of organ donors and to reconstruct at least parts of injured or diseased tissues or organs. However, oxygen and nutrient supply are limiting factors in many tissues, especially after implantation into the host. Therefore, the development of a vascular system prior to implantation appears crucial. To develop a functional vascular system, different cell types that interact with each other need to be co-cultured to simulate a physiological environment in vitro. This review provides an overview and a comparison of the current knowledge of co-cultures of human endothelial cells (ECs) with human adipose tissue-derived stem/stromal cells (ASCs) or bone marrow-mesenchymal stem cells (BMSCs) in three dimensional (3D) hydrogel matrices. Mesenchymal stem cells (MSCs), BMSCs or ASCs, have been shown to enhance vascular tube formation of ECs and to provide a stabilizing function in addition to growth factor delivery and permeability control for ECs. Although phenotypically similar, MSCs from different tissues promote tubulogenesis through distinct mechanisms. In this report, we describe differences and similarities regarding molecular interactions in order to investigate which of these two cell types displays more favorable characteristics to be used in clinical applications. Our comparative study shows that ASCs as well as BMSCs are both promising cell types to induce vascularization with ECs in vitro and consequently are promising candidates to support in vivo vascularization. |
format | Online Article Text |
id | pubmed-4619361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46193612015-10-26 Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison Pill, Karoline Hofmann, Sandra Redl, Heinz Holnthoner, Wolfgang Cell Regen Review Tissue-engineered constructs are promising to overcome shortage of organ donors and to reconstruct at least parts of injured or diseased tissues or organs. However, oxygen and nutrient supply are limiting factors in many tissues, especially after implantation into the host. Therefore, the development of a vascular system prior to implantation appears crucial. To develop a functional vascular system, different cell types that interact with each other need to be co-cultured to simulate a physiological environment in vitro. This review provides an overview and a comparison of the current knowledge of co-cultures of human endothelial cells (ECs) with human adipose tissue-derived stem/stromal cells (ASCs) or bone marrow-mesenchymal stem cells (BMSCs) in three dimensional (3D) hydrogel matrices. Mesenchymal stem cells (MSCs), BMSCs or ASCs, have been shown to enhance vascular tube formation of ECs and to provide a stabilizing function in addition to growth factor delivery and permeability control for ECs. Although phenotypically similar, MSCs from different tissues promote tubulogenesis through distinct mechanisms. In this report, we describe differences and similarities regarding molecular interactions in order to investigate which of these two cell types displays more favorable characteristics to be used in clinical applications. Our comparative study shows that ASCs as well as BMSCs are both promising cell types to induce vascularization with ECs in vitro and consequently are promising candidates to support in vivo vascularization. BioMed Central 2015-10-23 /pmc/articles/PMC4619361/ /pubmed/26500761 http://dx.doi.org/10.1186/s13619-015-0025-8 Text en © Pill et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Review Pill, Karoline Hofmann, Sandra Redl, Heinz Holnthoner, Wolfgang Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
title | Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
title_full | Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
title_fullStr | Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
title_full_unstemmed | Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
title_short | Vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
title_sort | vascularization mediated by mesenchymal stem cells from bone marrow and adipose tissue: a comparison |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619361/ https://www.ncbi.nlm.nih.gov/pubmed/26500761 http://dx.doi.org/10.1186/s13619-015-0025-8 |
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