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In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells

Directing angiogenic differentiation of mesenchymal stem cells (MSCs) still remains challenging for successful tissue engineering. Without blood vessel formation, stem cell-based approaches are unable to fully regenerate damaged tissues due to limited support for cell viability and desired tissue/or...

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Autores principales: Lee, Yunki, Balikov, Daniel A., Lee, Jung Bok, Lee, Sue Hyun, Lee, Seung Hwan, Lee, Jong Hun, Park, Ki Dong, Sung, Hak-Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578095/
https://www.ncbi.nlm.nih.gov/pubmed/28777301
http://dx.doi.org/10.3390/ijms18081705
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author Lee, Yunki
Balikov, Daniel A.
Lee, Jung Bok
Lee, Sue Hyun
Lee, Seung Hwan
Lee, Jong Hun
Park, Ki Dong
Sung, Hak-Joon
author_facet Lee, Yunki
Balikov, Daniel A.
Lee, Jung Bok
Lee, Sue Hyun
Lee, Seung Hwan
Lee, Jong Hun
Park, Ki Dong
Sung, Hak-Joon
author_sort Lee, Yunki
collection PubMed
description Directing angiogenic differentiation of mesenchymal stem cells (MSCs) still remains challenging for successful tissue engineering. Without blood vessel formation, stem cell-based approaches are unable to fully regenerate damaged tissues due to limited support for cell viability and desired tissue/organ functionality. Herein, we report in situ cross-linkable gelatin−hydroxyphenyl propionic acid (GH) hydrogels that can induce pro-angiogenic profiles of MSCs via purely material-driven effects. This hydrogel directed endothelial differentiation of mouse and human patient-derived MSCs through integrin-mediated interactions at the cell-material interface, thereby promoting perfusable blood vessel formation in vitro and in vivo. The causative roles of specific integrin types (α(1) and α(v)β(3)) in directing endothelial differentiation were verified by blocking the integrin functions with chemical inhibitors. In addition, to verify the material-driven effect is not species-specific, we confirmed in vitro endothelial differentiation and in vivo blood vessel formation of patient-derived human MSCs by this hydrogel. These findings provide new insight into how purely material-driven effects can direct endothelial differentiation of MSCs, thereby promoting vascularization of scaffolds towards tissue engineering and regenerative medicine applications in humans.
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spelling pubmed-55780952017-09-05 In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells Lee, Yunki Balikov, Daniel A. Lee, Jung Bok Lee, Sue Hyun Lee, Seung Hwan Lee, Jong Hun Park, Ki Dong Sung, Hak-Joon Int J Mol Sci Article Directing angiogenic differentiation of mesenchymal stem cells (MSCs) still remains challenging for successful tissue engineering. Without blood vessel formation, stem cell-based approaches are unable to fully regenerate damaged tissues due to limited support for cell viability and desired tissue/organ functionality. Herein, we report in situ cross-linkable gelatin−hydroxyphenyl propionic acid (GH) hydrogels that can induce pro-angiogenic profiles of MSCs via purely material-driven effects. This hydrogel directed endothelial differentiation of mouse and human patient-derived MSCs through integrin-mediated interactions at the cell-material interface, thereby promoting perfusable blood vessel formation in vitro and in vivo. The causative roles of specific integrin types (α(1) and α(v)β(3)) in directing endothelial differentiation were verified by blocking the integrin functions with chemical inhibitors. In addition, to verify the material-driven effect is not species-specific, we confirmed in vitro endothelial differentiation and in vivo blood vessel formation of patient-derived human MSCs by this hydrogel. These findings provide new insight into how purely material-driven effects can direct endothelial differentiation of MSCs, thereby promoting vascularization of scaffolds towards tissue engineering and regenerative medicine applications in humans. MDPI 2017-08-04 /pmc/articles/PMC5578095/ /pubmed/28777301 http://dx.doi.org/10.3390/ijms18081705 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Yunki
Balikov, Daniel A.
Lee, Jung Bok
Lee, Sue Hyun
Lee, Seung Hwan
Lee, Jong Hun
Park, Ki Dong
Sung, Hak-Joon
In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells
title In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells
title_full In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells
title_fullStr In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells
title_full_unstemmed In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells
title_short In Situ Forming Gelatin Hydrogels-Directed Angiogenic Differentiation and Activity of Patient-Derived Human Mesenchymal Stem Cells
title_sort in situ forming gelatin hydrogels-directed angiogenic differentiation and activity of patient-derived human mesenchymal stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578095/
https://www.ncbi.nlm.nih.gov/pubmed/28777301
http://dx.doi.org/10.3390/ijms18081705
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