Cargando…

Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering

Induced pluripotent stem cells (iPSC) hold tremendous potential for personalized cell-based therapy for skin regeneration. Aiming to establish human iPSCs as a potential cell source for skin tissue engineering, we expect to obtain an epidermal-like cell line with angiogenic and keratinogenic differe...

Descripción completa

Detalles Bibliográficos
Autores principales: Lin, Weimin, Chen, Miao, Hu, Chen, Qin, Siyu, Chu, Chenyu, Xiang, Lin, Man, Yi, Qu, Yili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158941/
https://www.ncbi.nlm.nih.gov/pubmed/30302340
http://dx.doi.org/10.1155/2018/8459503
_version_ 1783358521284231168
author Lin, Weimin
Chen, Miao
Hu, Chen
Qin, Siyu
Chu, Chenyu
Xiang, Lin
Man, Yi
Qu, Yili
author_facet Lin, Weimin
Chen, Miao
Hu, Chen
Qin, Siyu
Chu, Chenyu
Xiang, Lin
Man, Yi
Qu, Yili
author_sort Lin, Weimin
collection PubMed
description Induced pluripotent stem cells (iPSC) hold tremendous potential for personalized cell-based therapy for skin regeneration. Aiming to establish human iPSCs as a potential cell source for skin tissue engineering, we expect to obtain an epidermal-like cell line with angiogenic and keratinogenic differentiation potential via inducing iPSC-derived mesenchymal stem cells (iPSC-MSCs) with basic fibroblast growth factor (bFGF) and/or keratinocyte growth factor (KGF). The results show that iPSC-MSCs were successfully induced with a positive FGFR/KGFR expression on the cell surface. BFGF/KGF induction could significantly increase the expression of vascularization marker CD31 and keratinization marker CK10, respectively, while when combined together, although CD31 and CK10 were still positively expressed, their expressions were lower than that of the single induction group, suggesting that the effects of the two growth factors interfered with each other. This cell line with angiogenic and keratinogenic differentiation potential provides a promising new source of cells for the construction of well vascularized and keratinized tissue engineered skin, furthermore establishing an effective strategy for iPSC-based therapy in skin tissue engineering.
format Online
Article
Text
id pubmed-6158941
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-61589412018-10-09 Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering Lin, Weimin Chen, Miao Hu, Chen Qin, Siyu Chu, Chenyu Xiang, Lin Man, Yi Qu, Yili Biomed Res Int Research Article Induced pluripotent stem cells (iPSC) hold tremendous potential for personalized cell-based therapy for skin regeneration. Aiming to establish human iPSCs as a potential cell source for skin tissue engineering, we expect to obtain an epidermal-like cell line with angiogenic and keratinogenic differentiation potential via inducing iPSC-derived mesenchymal stem cells (iPSC-MSCs) with basic fibroblast growth factor (bFGF) and/or keratinocyte growth factor (KGF). The results show that iPSC-MSCs were successfully induced with a positive FGFR/KGFR expression on the cell surface. BFGF/KGF induction could significantly increase the expression of vascularization marker CD31 and keratinization marker CK10, respectively, while when combined together, although CD31 and CK10 were still positively expressed, their expressions were lower than that of the single induction group, suggesting that the effects of the two growth factors interfered with each other. This cell line with angiogenic and keratinogenic differentiation potential provides a promising new source of cells for the construction of well vascularized and keratinized tissue engineered skin, furthermore establishing an effective strategy for iPSC-based therapy in skin tissue engineering. Hindawi 2018-09-13 /pmc/articles/PMC6158941/ /pubmed/30302340 http://dx.doi.org/10.1155/2018/8459503 Text en Copyright © 2018 Weimin Lin et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lin, Weimin
Chen, Miao
Hu, Chen
Qin, Siyu
Chu, Chenyu
Xiang, Lin
Man, Yi
Qu, Yili
Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering
title Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering
title_full Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering
title_fullStr Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering
title_full_unstemmed Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering
title_short Endowing iPSC-Derived MSCs with Angiogenic and Keratinogenic Differentiation Potential: A Promising Cell Source for Skin Tissue Engineering
title_sort endowing ipsc-derived mscs with angiogenic and keratinogenic differentiation potential: a promising cell source for skin tissue engineering
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158941/
https://www.ncbi.nlm.nih.gov/pubmed/30302340
http://dx.doi.org/10.1155/2018/8459503
work_keys_str_mv AT linweimin endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT chenmiao endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT huchen endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT qinsiyu endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT chuchenyu endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT xianglin endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT manyi endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering
AT quyili endowingipscderivedmscswithangiogenicandkeratinogenicdifferentiationpotentialapromisingcellsourceforskintissueengineering