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Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture
A well-organised vascular network is essential for metabolic exchange to maintain homoeostasis in the body. Therefore, for progress in regenerative medicine, it is particularly important to establish methods of vascularization in bioengineered three-dimensional (3D) functional tissues. In addition,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222294/ https://www.ncbi.nlm.nih.gov/pubmed/30525069 http://dx.doi.org/10.1016/j.reth.2018.06.004 |
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author | Masuda, Shinako Matsuura, Katsuhisa Shimizu, Tatsuya |
author_facet | Masuda, Shinako Matsuura, Katsuhisa Shimizu, Tatsuya |
author_sort | Masuda, Shinako |
collection | PubMed |
description | A well-organised vascular network is essential for metabolic exchange to maintain homoeostasis in the body. Therefore, for progress in regenerative medicine, it is particularly important to establish methods of vascularization in bioengineered three-dimensional (3D) functional tissues. In addition, it is necessary to develop methods to supply a large number of iPS cell-derived endothelial cells for fabricating the vascular network structure. There are already many reports on the method of inducing the differentiation of endothelial cells from iPS cells using 2D culture. However, there are few reports on methods for preparing a large number of iPS cell-derived endothelial cells. Therefore, we developed methods for inducing vascular endothelial cells from human inducible pluripotent stem (hiPS) cells using 3D suspension culture. hiPS cell-derived CD31(+) cells expressed several endothelial marker genes and formed endothelial cell network structures, similar to human umbilical vein endothelial cells. These results indicate that hiPS cell-derived CD31(+) cells may be a useful cell source for pre-vascularised network structures in 3D functional tissues, and it is important to develop 3D mass culture system for preparing a large number of cells to fabricate bioengineered tissues. |
format | Online Article Text |
id | pubmed-6222294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-62222942018-12-06 Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture Masuda, Shinako Matsuura, Katsuhisa Shimizu, Tatsuya Regen Ther Original Article A well-organised vascular network is essential for metabolic exchange to maintain homoeostasis in the body. Therefore, for progress in regenerative medicine, it is particularly important to establish methods of vascularization in bioengineered three-dimensional (3D) functional tissues. In addition, it is necessary to develop methods to supply a large number of iPS cell-derived endothelial cells for fabricating the vascular network structure. There are already many reports on the method of inducing the differentiation of endothelial cells from iPS cells using 2D culture. However, there are few reports on methods for preparing a large number of iPS cell-derived endothelial cells. Therefore, we developed methods for inducing vascular endothelial cells from human inducible pluripotent stem (hiPS) cells using 3D suspension culture. hiPS cell-derived CD31(+) cells expressed several endothelial marker genes and formed endothelial cell network structures, similar to human umbilical vein endothelial cells. These results indicate that hiPS cell-derived CD31(+) cells may be a useful cell source for pre-vascularised network structures in 3D functional tissues, and it is important to develop 3D mass culture system for preparing a large number of cells to fabricate bioengineered tissues. Japanese Society for Regenerative Medicine 2018-07-07 /pmc/articles/PMC6222294/ /pubmed/30525069 http://dx.doi.org/10.1016/j.reth.2018.06.004 Text en © 2018 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Masuda, Shinako Matsuura, Katsuhisa Shimizu, Tatsuya Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture |
title | Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture |
title_full | Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture |
title_fullStr | Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture |
title_full_unstemmed | Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture |
title_short | Preparation of iPS cell-derived CD31(+) endothelial cells using three-dimensional suspension culture |
title_sort | preparation of ips cell-derived cd31(+) endothelial cells using three-dimensional suspension culture |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222294/ https://www.ncbi.nlm.nih.gov/pubmed/30525069 http://dx.doi.org/10.1016/j.reth.2018.06.004 |
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