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Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch

BACKGROUND: In vitro generation of three-dimensional vessel network is crucial to investigate and possibly improve vascularization after implantation in vivo. This work has the purpose of engineering complex tissue regeneration of a vascular network including multiple cell-type, an extracellular mat...

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Autores principales: Hong, Soyoung, Song, Yejin, Choi, Jaesoon, Hwang, Changmo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971335/
https://www.ncbi.nlm.nih.gov/pubmed/34870799
http://dx.doi.org/10.1007/s13770-021-00409-1
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author Hong, Soyoung
Song, Yejin
Choi, Jaesoon
Hwang, Changmo
author_facet Hong, Soyoung
Song, Yejin
Choi, Jaesoon
Hwang, Changmo
author_sort Hong, Soyoung
collection PubMed
description BACKGROUND: In vitro generation of three-dimensional vessel network is crucial to investigate and possibly improve vascularization after implantation in vivo. This work has the purpose of engineering complex tissue regeneration of a vascular network including multiple cell-type, an extracellular matrix, and perfusability for clinical application. METHODS: The two electrospun membranes bonded with the vascular network shape are cultured with endothelial cells and medium flow through the engineered vascular network. The flexible membranes are bonded by amine-epoxy reaction and examined the perfusability with fluorescent beads. Also, the perfusion culture for 7 days of the endothelial cells is compared with static culture on the engineered vascular network membrane. RESULTS: The engineered membranes are showed perfusability through the vascular network, and the perfused network resulted in more cell proliferation and variation of the shear stress-related genes expression compared to the static culture. Also, for the generation of the complex vascularized network, pericytes are co-cultured with the engineered vascular network, which results in the Collagen I is expressed on the outer surface of the engineered structure. CONCLUSION: This study is showing the perfusable in vitro engineered vascular network with electrospun membrane. In further, the 3D vascularized network module can be expected as a platform for drug screening and regenerative medicine. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13770-021-00409-1.
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spelling pubmed-89713352022-04-20 Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch Hong, Soyoung Song, Yejin Choi, Jaesoon Hwang, Changmo Tissue Eng Regen Med Original Article BACKGROUND: In vitro generation of three-dimensional vessel network is crucial to investigate and possibly improve vascularization after implantation in vivo. This work has the purpose of engineering complex tissue regeneration of a vascular network including multiple cell-type, an extracellular matrix, and perfusability for clinical application. METHODS: The two electrospun membranes bonded with the vascular network shape are cultured with endothelial cells and medium flow through the engineered vascular network. The flexible membranes are bonded by amine-epoxy reaction and examined the perfusability with fluorescent beads. Also, the perfusion culture for 7 days of the endothelial cells is compared with static culture on the engineered vascular network membrane. RESULTS: The engineered membranes are showed perfusability through the vascular network, and the perfused network resulted in more cell proliferation and variation of the shear stress-related genes expression compared to the static culture. Also, for the generation of the complex vascularized network, pericytes are co-cultured with the engineered vascular network, which results in the Collagen I is expressed on the outer surface of the engineered structure. CONCLUSION: This study is showing the perfusable in vitro engineered vascular network with electrospun membrane. In further, the 3D vascularized network module can be expected as a platform for drug screening and regenerative medicine. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13770-021-00409-1. Springer Singapore 2021-12-06 /pmc/articles/PMC8971335/ /pubmed/34870799 http://dx.doi.org/10.1007/s13770-021-00409-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Hong, Soyoung
Song, Yejin
Choi, Jaesoon
Hwang, Changmo
Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch
title Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch
title_full Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch
title_fullStr Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch
title_full_unstemmed Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch
title_short Bonding of Flexible Membranes for Perfusable Vascularized Networks Patch
title_sort bonding of flexible membranes for perfusable vascularized networks patch
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971335/
https://www.ncbi.nlm.nih.gov/pubmed/34870799
http://dx.doi.org/10.1007/s13770-021-00409-1
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