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Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft
Tissue engineered vascular grafts (TEVG) are potentially clear from ethical and epidemiological concerns sources for reconstructive surgery for small diameter blood vessels replacement. Here, we proposed a novel method to create three-layered TEVG on biocompatible glass fiber scaffolds starting from...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290030/ https://www.ncbi.nlm.nih.gov/pubmed/34282200 http://dx.doi.org/10.1038/s41598-021-94023-9 |
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author | Baba, Kazutomo Mikhailov, Andrey Sankai, Yoshiyuki |
author_facet | Baba, Kazutomo Mikhailov, Andrey Sankai, Yoshiyuki |
author_sort | Baba, Kazutomo |
collection | PubMed |
description | Tissue engineered vascular grafts (TEVG) are potentially clear from ethical and epidemiological concerns sources for reconstructive surgery for small diameter blood vessels replacement. Here, we proposed a novel method to create three-layered TEVG on biocompatible glass fiber scaffolds starting from flat sheet state into tubular shape and to train the resulting tissue by our developed bioreactor system. Constructed tubular tissues were matured and trained under 3 types of individual flow programs, and their mechanical and biological properties were analyzed. Training in the bioreactor significantly increased the tissue burst pressure resistance (up to 18 kPa) comparing to untrained tissue. Fluorescent imaging and histological examination of trained vascular tissue revealed that each cell layer has its own individual response to training flow rates. Histological analysis suggested reverse relationship between tissue thickness and shear stress, and the thickness variation profiles were individual between all three types of cell layers. Concluding: a three-layered tissue structure similar to physiological can be assembled by seeding different cell types in succession; the following training of the formed tissue with increasing flow in a bioreactor is effective for promoting cell survival, improving pressure resistance, and cell layer formation of desired properties. |
format | Online Article Text |
id | pubmed-8290030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82900302021-07-21 Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft Baba, Kazutomo Mikhailov, Andrey Sankai, Yoshiyuki Sci Rep Article Tissue engineered vascular grafts (TEVG) are potentially clear from ethical and epidemiological concerns sources for reconstructive surgery for small diameter blood vessels replacement. Here, we proposed a novel method to create three-layered TEVG on biocompatible glass fiber scaffolds starting from flat sheet state into tubular shape and to train the resulting tissue by our developed bioreactor system. Constructed tubular tissues were matured and trained under 3 types of individual flow programs, and their mechanical and biological properties were analyzed. Training in the bioreactor significantly increased the tissue burst pressure resistance (up to 18 kPa) comparing to untrained tissue. Fluorescent imaging and histological examination of trained vascular tissue revealed that each cell layer has its own individual response to training flow rates. Histological analysis suggested reverse relationship between tissue thickness and shear stress, and the thickness variation profiles were individual between all three types of cell layers. Concluding: a three-layered tissue structure similar to physiological can be assembled by seeding different cell types in succession; the following training of the formed tissue with increasing flow in a bioreactor is effective for promoting cell survival, improving pressure resistance, and cell layer formation of desired properties. Nature Publishing Group UK 2021-07-19 /pmc/articles/PMC8290030/ /pubmed/34282200 http://dx.doi.org/10.1038/s41598-021-94023-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 | Article Baba, Kazutomo Mikhailov, Andrey Sankai, Yoshiyuki Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
title | Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
title_full | Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
title_fullStr | Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
title_full_unstemmed | Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
title_short | Dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
title_sort | dynamic flow priming programs allow tuning up the cell layers properties for engineered vascular graft |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290030/ https://www.ncbi.nlm.nih.gov/pubmed/34282200 http://dx.doi.org/10.1038/s41598-021-94023-9 |
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