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Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats

The aim of the present study was to evaluate the anti-aging effects of bone marrow-mesenchymal stem cells (BM-MSCs) in a D-galactose-induced skin aging rat model. Male Sprague Dawley rats were randomly divided into four groups (n=10/group) as follows: Normal control group; skin aging model group; MS...

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Autores principales: Liu, Zhen, Hu, Guo-Dong, Luo, Xiao-Bo, Yin, Bin, Shu, Bin, Guan, Jing-Zhi, Jia, Chi-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403304/
https://www.ncbi.nlm.nih.gov/pubmed/28451386
http://dx.doi.org/10.3892/br.2017.842
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author Liu, Zhen
Hu, Guo-Dong
Luo, Xiao-Bo
Yin, Bin
Shu, Bin
Guan, Jing-Zhi
Jia, Chi-Yu
author_facet Liu, Zhen
Hu, Guo-Dong
Luo, Xiao-Bo
Yin, Bin
Shu, Bin
Guan, Jing-Zhi
Jia, Chi-Yu
author_sort Liu, Zhen
collection PubMed
description The aim of the present study was to evaluate the anti-aging effects of bone marrow-mesenchymal stem cells (BM-MSCs) in a D-galactose-induced skin aging rat model. Male Sprague Dawley rats were randomly divided into four groups (n=10/group) as follows: Normal control group; skin aging model group; MSC-treated group by subcutaneous multi-point injection. The skin aging model was established by a daily subcutaneous injection of 15% D-galactose (1,000 mg/kg) for 8 weeks. Rats in the MSC-treated groups were administered 3×10(6)/ml BM-MSCs/green fluorescent protein (GFP) for 4 weeks, administered once per week. Oxidative/antioxidative parameters were evaluated, and morphological and ultrastructure analyses were performed. Rats in the model group exhibited the typical changes of aging skin. Compared with the control group, rats in the model group had significantly increased malondialdehyde (MDA) content (P<0.01), and decreased serum superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities (P<0.05). MSC treatment markedly ameliorated aging-induced oxidative stress in the skin. Histologically, rats in the model group exhibited loosely arranged epidermal cell layers and disorganized collagen fibers. BM-MSC treatment significantly improved the histological abnormalities, which was similar to those in the control group. In addition, 7 days after the final cell transplantation, GFP-positive cells were observed by fluorescence microscopy to be distributed in the dermis. Injection of BM-MSCs significantly improved the D-galactose-induced histological abnormalities of the skin, by promoting an antioxidant response and ameliorating oxidative stress in aged skin. Thus, BM-MSCs may be beneficial in the rejuvenation of aged skin.
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spelling pubmed-54033042017-04-27 Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats Liu, Zhen Hu, Guo-Dong Luo, Xiao-Bo Yin, Bin Shu, Bin Guan, Jing-Zhi Jia, Chi-Yu Biomed Rep Articles The aim of the present study was to evaluate the anti-aging effects of bone marrow-mesenchymal stem cells (BM-MSCs) in a D-galactose-induced skin aging rat model. Male Sprague Dawley rats were randomly divided into four groups (n=10/group) as follows: Normal control group; skin aging model group; MSC-treated group by subcutaneous multi-point injection. The skin aging model was established by a daily subcutaneous injection of 15% D-galactose (1,000 mg/kg) for 8 weeks. Rats in the MSC-treated groups were administered 3×10(6)/ml BM-MSCs/green fluorescent protein (GFP) for 4 weeks, administered once per week. Oxidative/antioxidative parameters were evaluated, and morphological and ultrastructure analyses were performed. Rats in the model group exhibited the typical changes of aging skin. Compared with the control group, rats in the model group had significantly increased malondialdehyde (MDA) content (P<0.01), and decreased serum superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities (P<0.05). MSC treatment markedly ameliorated aging-induced oxidative stress in the skin. Histologically, rats in the model group exhibited loosely arranged epidermal cell layers and disorganized collagen fibers. BM-MSC treatment significantly improved the histological abnormalities, which was similar to those in the control group. In addition, 7 days after the final cell transplantation, GFP-positive cells were observed by fluorescence microscopy to be distributed in the dermis. Injection of BM-MSCs significantly improved the D-galactose-induced histological abnormalities of the skin, by promoting an antioxidant response and ameliorating oxidative stress in aged skin. Thus, BM-MSCs may be beneficial in the rejuvenation of aged skin. D.A. Spandidos 2017-03 2017-01-13 /pmc/articles/PMC5403304/ /pubmed/28451386 http://dx.doi.org/10.3892/br.2017.842 Text en Copyright: © Liu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Liu, Zhen
Hu, Guo-Dong
Luo, Xiao-Bo
Yin, Bin
Shu, Bin
Guan, Jing-Zhi
Jia, Chi-Yu
Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
title Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
title_full Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
title_fullStr Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
title_full_unstemmed Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
title_short Potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
title_sort potential of bone marrow mesenchymal stem cells in rejuvenation of the aged skin of rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403304/
https://www.ncbi.nlm.nih.gov/pubmed/28451386
http://dx.doi.org/10.3892/br.2017.842
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