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Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels
Tissue-engineered blood vessels (TEBV) can serve as vascular grafts and may also play an important role in the development of organs-on-a-chip. Most TEBV construction involves scaffolding with biomaterials such as collagen gel or electrospun fibrous mesh. Hypothesizing that a scaffold-free TEBV may...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600980/ https://www.ncbi.nlm.nih.gov/pubmed/26456074 http://dx.doi.org/10.1038/srep15116 |
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author | Jung, Youngmee Ji, HaYeun Chen, Zaozao Fai Chan, Hon Atchison, Leigh Klitzman, Bruce Truskey, George Leong, Kam W. |
author_facet | Jung, Youngmee Ji, HaYeun Chen, Zaozao Fai Chan, Hon Atchison, Leigh Klitzman, Bruce Truskey, George Leong, Kam W. |
author_sort | Jung, Youngmee |
collection | PubMed |
description | Tissue-engineered blood vessels (TEBV) can serve as vascular grafts and may also play an important role in the development of organs-on-a-chip. Most TEBV construction involves scaffolding with biomaterials such as collagen gel or electrospun fibrous mesh. Hypothesizing that a scaffold-free TEBV may be advantageous, we constructed a tubular structure (1 mm i.d.) from aligned human mesenchymal cell sheets (hMSC) as the wall and human endothelial progenitor cell (hEPC) coating as the lumen. The burst pressure of the scaffold-free TEBV was above 200 mmHg after three weeks of sequential culture in a rotating wall bioreactor and perfusion at 6.8 dynes/cm(2). The interwoven organization of the cell layers and extensive extracellular matrix (ECM) formation of the hMSC-based TEBV resembled that of native blood vessels. The TEBV exhibited flow-mediated vasodilation, vasoconstriction after exposure to 1 μM phenylephrine and released nitric oxide in a manner similar to that of porcine femoral vein. HL-60 cells attached to the TEBV lumen after TNF-α activation to suggest a functional endothelium. This study demonstrates the potential of a hEPC endothelialized hMSC-based TEBV for drug screening. |
format | Online Article Text |
id | pubmed-4600980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46009802015-10-21 Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels Jung, Youngmee Ji, HaYeun Chen, Zaozao Fai Chan, Hon Atchison, Leigh Klitzman, Bruce Truskey, George Leong, Kam W. Sci Rep Article Tissue-engineered blood vessels (TEBV) can serve as vascular grafts and may also play an important role in the development of organs-on-a-chip. Most TEBV construction involves scaffolding with biomaterials such as collagen gel or electrospun fibrous mesh. Hypothesizing that a scaffold-free TEBV may be advantageous, we constructed a tubular structure (1 mm i.d.) from aligned human mesenchymal cell sheets (hMSC) as the wall and human endothelial progenitor cell (hEPC) coating as the lumen. The burst pressure of the scaffold-free TEBV was above 200 mmHg after three weeks of sequential culture in a rotating wall bioreactor and perfusion at 6.8 dynes/cm(2). The interwoven organization of the cell layers and extensive extracellular matrix (ECM) formation of the hMSC-based TEBV resembled that of native blood vessels. The TEBV exhibited flow-mediated vasodilation, vasoconstriction after exposure to 1 μM phenylephrine and released nitric oxide in a manner similar to that of porcine femoral vein. HL-60 cells attached to the TEBV lumen after TNF-α activation to suggest a functional endothelium. This study demonstrates the potential of a hEPC endothelialized hMSC-based TEBV for drug screening. Nature Publishing Group 2015-10-12 /pmc/articles/PMC4600980/ /pubmed/26456074 http://dx.doi.org/10.1038/srep15116 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jung, Youngmee Ji, HaYeun Chen, Zaozao Fai Chan, Hon Atchison, Leigh Klitzman, Bruce Truskey, George Leong, Kam W. Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels |
title | Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels |
title_full | Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels |
title_fullStr | Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels |
title_full_unstemmed | Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels |
title_short | Scaffold-free, Human Mesenchymal Stem Cell-Based Tissue Engineered Blood Vessels |
title_sort | scaffold-free, human mesenchymal stem cell-based tissue engineered blood vessels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600980/ https://www.ncbi.nlm.nih.gov/pubmed/26456074 http://dx.doi.org/10.1038/srep15116 |
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