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Adipose-derived stromal/stem cells improve epidermal homeostasis

Wound healing is regulated by complex interactions between the keratinocytes and other cell types including fibroblasts. Recently, adipose-derived mesenchymal stromal/stem cells (ASCs) have been reported to influence wound healing positively via paracrine involvement. However, their roles in keratin...

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Autores principales: Moriyama, Mariko, Sahara, Shunya, Zaiki, Kaori, Ueno, Ayumi, Nakaoji, Koichi, Hamada, Kazuhiko, Ozawa, Toshiyuki, Tsuruta, Daisuke, Hayakawa, Takao, Moriyama, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892794/
https://www.ncbi.nlm.nih.gov/pubmed/31797970
http://dx.doi.org/10.1038/s41598-019-54797-5
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author Moriyama, Mariko
Sahara, Shunya
Zaiki, Kaori
Ueno, Ayumi
Nakaoji, Koichi
Hamada, Kazuhiko
Ozawa, Toshiyuki
Tsuruta, Daisuke
Hayakawa, Takao
Moriyama, Hiroyuki
author_facet Moriyama, Mariko
Sahara, Shunya
Zaiki, Kaori
Ueno, Ayumi
Nakaoji, Koichi
Hamada, Kazuhiko
Ozawa, Toshiyuki
Tsuruta, Daisuke
Hayakawa, Takao
Moriyama, Hiroyuki
author_sort Moriyama, Mariko
collection PubMed
description Wound healing is regulated by complex interactions between the keratinocytes and other cell types including fibroblasts. Recently, adipose-derived mesenchymal stromal/stem cells (ASCs) have been reported to influence wound healing positively via paracrine involvement. However, their roles in keratinocytes are still obscure. Therefore, investigation of the precise effects of ASCs on keratinocytes in an in vitro culture system is required. Our recent data indicate that the epidermal equivalents became thicker on a collagen vitrigel membrane co-cultured with human ASCs (hASCs). Co-culturing the human primary epidermal keratinocytes (HPEK) with hASCs on a collagen vitrigel membrane enhanced their abilities for cell proliferation and adhesion to the membrane but suppressed their differentiation suggesting that hASCs could maintain the undifferentiated status of HPEK. Contrarily, the effects of co-culture using polyethylene terephthalate or polycarbonate membranes for HPEK were completely opposite. These differences may depend on the protein permeability and/or structure of the membrane. Taken together, our data demonstrate that hASCs could be used as a substitute for fibroblasts in skin wound repair, aesthetic medicine, or tissue engineering. It is also important to note that a co-culture system using the collagen vitrigel membrane allows better understanding of the interactions between the keratinocytes and ASCs.
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spelling pubmed-68927942019-12-10 Adipose-derived stromal/stem cells improve epidermal homeostasis Moriyama, Mariko Sahara, Shunya Zaiki, Kaori Ueno, Ayumi Nakaoji, Koichi Hamada, Kazuhiko Ozawa, Toshiyuki Tsuruta, Daisuke Hayakawa, Takao Moriyama, Hiroyuki Sci Rep Article Wound healing is regulated by complex interactions between the keratinocytes and other cell types including fibroblasts. Recently, adipose-derived mesenchymal stromal/stem cells (ASCs) have been reported to influence wound healing positively via paracrine involvement. However, their roles in keratinocytes are still obscure. Therefore, investigation of the precise effects of ASCs on keratinocytes in an in vitro culture system is required. Our recent data indicate that the epidermal equivalents became thicker on a collagen vitrigel membrane co-cultured with human ASCs (hASCs). Co-culturing the human primary epidermal keratinocytes (HPEK) with hASCs on a collagen vitrigel membrane enhanced their abilities for cell proliferation and adhesion to the membrane but suppressed their differentiation suggesting that hASCs could maintain the undifferentiated status of HPEK. Contrarily, the effects of co-culture using polyethylene terephthalate or polycarbonate membranes for HPEK were completely opposite. These differences may depend on the protein permeability and/or structure of the membrane. Taken together, our data demonstrate that hASCs could be used as a substitute for fibroblasts in skin wound repair, aesthetic medicine, or tissue engineering. It is also important to note that a co-culture system using the collagen vitrigel membrane allows better understanding of the interactions between the keratinocytes and ASCs. Nature Publishing Group UK 2019-12-04 /pmc/articles/PMC6892794/ /pubmed/31797970 http://dx.doi.org/10.1038/s41598-019-54797-5 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Moriyama, Mariko
Sahara, Shunya
Zaiki, Kaori
Ueno, Ayumi
Nakaoji, Koichi
Hamada, Kazuhiko
Ozawa, Toshiyuki
Tsuruta, Daisuke
Hayakawa, Takao
Moriyama, Hiroyuki
Adipose-derived stromal/stem cells improve epidermal homeostasis
title Adipose-derived stromal/stem cells improve epidermal homeostasis
title_full Adipose-derived stromal/stem cells improve epidermal homeostasis
title_fullStr Adipose-derived stromal/stem cells improve epidermal homeostasis
title_full_unstemmed Adipose-derived stromal/stem cells improve epidermal homeostasis
title_short Adipose-derived stromal/stem cells improve epidermal homeostasis
title_sort adipose-derived stromal/stem cells improve epidermal homeostasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892794/
https://www.ncbi.nlm.nih.gov/pubmed/31797970
http://dx.doi.org/10.1038/s41598-019-54797-5
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