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Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell
Mesenchymal stem cells (MSCs) are considered a potential autologous therapy for tissue engineering. The available procedures for MSC retrieval from patients are invasive, and their limited in vitro proliferation restricts their use in the treatment of damaged tissues. Therefore, it is important to e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490513/ https://www.ncbi.nlm.nih.gov/pubmed/26084043 http://dx.doi.org/10.3390/ijms160613633 |
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author | Umezaki, Yasuyuki Hashimoto, Yoshiya Nishishita, Naoki Kawamata, Shin Baba, Shunsuke |
author_facet | Umezaki, Yasuyuki Hashimoto, Yoshiya Nishishita, Naoki Kawamata, Shin Baba, Shunsuke |
author_sort | Umezaki, Yasuyuki |
collection | PubMed |
description | Mesenchymal stem cells (MSCs) are considered a potential autologous therapy for tissue engineering. The available procedures for MSC retrieval from patients are invasive, and their limited in vitro proliferation restricts their use in the treatment of damaged tissues. Therefore, it is important to establish an alternative and safe source of MSCs. The objective of this study was to demonstrate induced pluripotent stem cell (iPSC) generation from a combination of an accessible source tissue and an integration-free method; we also attempted the differentiation of iPSCs into MSC-like cells (MSLCs) for future autologous tissue engineering. iPSCs were derived from human gingival tissues, which are easily accessible in the field of dentistry, via the use of non-integrating episomal plasmids. Established iPSCs expressed embryonic stem (ES) cell-specific markers, as assessed by gene analysis and immunocytochemistry. Embryoid bodies and teratoma formation were formed from iPSCs, showing their capacity to differentiate into three germ layers. Furthermore, we were successful in differentiating iPSCs into MSLCs. They tested positively for their capacity of trilineage differentiation. Our results demonstrate that human gingival integration-free iPSCs, readily accessible stem cells generated using episomal plasmid vectors, are a promising source of MSLCs, which can be used in tissue regeneration. |
format | Online Article Text |
id | pubmed-4490513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44905132015-07-07 Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell Umezaki, Yasuyuki Hashimoto, Yoshiya Nishishita, Naoki Kawamata, Shin Baba, Shunsuke Int J Mol Sci Article Mesenchymal stem cells (MSCs) are considered a potential autologous therapy for tissue engineering. The available procedures for MSC retrieval from patients are invasive, and their limited in vitro proliferation restricts their use in the treatment of damaged tissues. Therefore, it is important to establish an alternative and safe source of MSCs. The objective of this study was to demonstrate induced pluripotent stem cell (iPSC) generation from a combination of an accessible source tissue and an integration-free method; we also attempted the differentiation of iPSCs into MSC-like cells (MSLCs) for future autologous tissue engineering. iPSCs were derived from human gingival tissues, which are easily accessible in the field of dentistry, via the use of non-integrating episomal plasmids. Established iPSCs expressed embryonic stem (ES) cell-specific markers, as assessed by gene analysis and immunocytochemistry. Embryoid bodies and teratoma formation were formed from iPSCs, showing their capacity to differentiate into three germ layers. Furthermore, we were successful in differentiating iPSCs into MSLCs. They tested positively for their capacity of trilineage differentiation. Our results demonstrate that human gingival integration-free iPSCs, readily accessible stem cells generated using episomal plasmid vectors, are a promising source of MSLCs, which can be used in tissue regeneration. MDPI 2015-06-15 /pmc/articles/PMC4490513/ /pubmed/26084043 http://dx.doi.org/10.3390/ijms160613633 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Umezaki, Yasuyuki Hashimoto, Yoshiya Nishishita, Naoki Kawamata, Shin Baba, Shunsuke Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell |
title | Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell |
title_full | Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell |
title_fullStr | Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell |
title_full_unstemmed | Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell |
title_short | Human Gingival Integration-Free iPSCs; a Source for MSC-Like Cell |
title_sort | human gingival integration-free ipscs; a source for msc-like cell |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490513/ https://www.ncbi.nlm.nih.gov/pubmed/26084043 http://dx.doi.org/10.3390/ijms160613633 |
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