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GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling
OBJECTIVE: Epidermal stem cells (EpSCs) can self-renew, which are responsible for the long-term maintenance of the skin, and it also plays a critical role in wound re-epithelization, but the mechanism underlying EpSCs proliferation is unclear. GDF-5, also known as BMP-14, is a member of the BMP fami...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792190/ https://www.ncbi.nlm.nih.gov/pubmed/33413682 http://dx.doi.org/10.1186/s13287-020-02106-7 |
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author | Zhao, Xiaohong Bian, Ruyu Wang, Fan Wang, Ying Li, Xue Guo, Yicheng Zhang, Xiaorong Luo, Gaoxing Zhan, Rixing |
author_facet | Zhao, Xiaohong Bian, Ruyu Wang, Fan Wang, Ying Li, Xue Guo, Yicheng Zhang, Xiaorong Luo, Gaoxing Zhan, Rixing |
author_sort | Zhao, Xiaohong |
collection | PubMed |
description | OBJECTIVE: Epidermal stem cells (EpSCs) can self-renew, which are responsible for the long-term maintenance of the skin, and it also plays a critical role in wound re-epithelization, but the mechanism underlying EpSCs proliferation is unclear. GDF-5, also known as BMP-14, is a member of the BMP family and can be used as a self-renewal supporter. Here, we studied the effects of GDF-5 on mouse EpSCs proliferation mechanism in wound healing. METHODS: Firstly, the effects of GDF-5 on EpSCs proliferation was tested by using CCK8 reagent and PCNA expression was analyzed by Western blotting. Secondly, we screened genes that promote EpSCs proliferation in the FOX and cyclin family by qPCR, and then the protein expression level of the selected genes was further analyzed by Western blotting. Thirdly, siRNA plasmids and pAdEasy adenovirus were transfected or infected, respectively, into mouse EpSCs to detect the effect of target genes on GDF-5-induced cell proliferation. Furthermore, we injected GDF-5 to a deep partial thickness burn mouse model for finding out whether EpSCs proliferation can be detected by immunohistochemical. Finally, the relevant target genes were analyzed by qPCR, immunoblotting, and dual-luciferase reporter gene detection. RESULTS: We discovered that 100 ng/ml recombinant mouse GDF-5 was the optimal concentration for promoting mouse EpSCs proliferation. Through preliminary screened by qPCR, we found that Foxg1 and cyclin D1 could be the downstream molecules of GDF-5, and the results were confirmed by Western blotting. And the effect of GDF-5 on mouse EpSCs proliferation was adjusted by Foxg1/cyclin D1 in vitro and in vivo. Besides, GDF-5-induced transcription of cyclin D1 was regulated by Foxg1-mediated cyclin D1 promoter activity. CONCLUSION: This paper showed that GDF-5 promotes mouse EpSCs proliferation via Foxg1-cyclin D1 signal pathway. It is suggested that GDF-5 may be a new approach to make EpSCs proliferation which can be used in wound healing. |
format | Online Article Text |
id | pubmed-7792190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77921902021-01-11 GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling Zhao, Xiaohong Bian, Ruyu Wang, Fan Wang, Ying Li, Xue Guo, Yicheng Zhang, Xiaorong Luo, Gaoxing Zhan, Rixing Stem Cell Res Ther Research OBJECTIVE: Epidermal stem cells (EpSCs) can self-renew, which are responsible for the long-term maintenance of the skin, and it also plays a critical role in wound re-epithelization, but the mechanism underlying EpSCs proliferation is unclear. GDF-5, also known as BMP-14, is a member of the BMP family and can be used as a self-renewal supporter. Here, we studied the effects of GDF-5 on mouse EpSCs proliferation mechanism in wound healing. METHODS: Firstly, the effects of GDF-5 on EpSCs proliferation was tested by using CCK8 reagent and PCNA expression was analyzed by Western blotting. Secondly, we screened genes that promote EpSCs proliferation in the FOX and cyclin family by qPCR, and then the protein expression level of the selected genes was further analyzed by Western blotting. Thirdly, siRNA plasmids and pAdEasy adenovirus were transfected or infected, respectively, into mouse EpSCs to detect the effect of target genes on GDF-5-induced cell proliferation. Furthermore, we injected GDF-5 to a deep partial thickness burn mouse model for finding out whether EpSCs proliferation can be detected by immunohistochemical. Finally, the relevant target genes were analyzed by qPCR, immunoblotting, and dual-luciferase reporter gene detection. RESULTS: We discovered that 100 ng/ml recombinant mouse GDF-5 was the optimal concentration for promoting mouse EpSCs proliferation. Through preliminary screened by qPCR, we found that Foxg1 and cyclin D1 could be the downstream molecules of GDF-5, and the results were confirmed by Western blotting. And the effect of GDF-5 on mouse EpSCs proliferation was adjusted by Foxg1/cyclin D1 in vitro and in vivo. Besides, GDF-5-induced transcription of cyclin D1 was regulated by Foxg1-mediated cyclin D1 promoter activity. CONCLUSION: This paper showed that GDF-5 promotes mouse EpSCs proliferation via Foxg1-cyclin D1 signal pathway. It is suggested that GDF-5 may be a new approach to make EpSCs proliferation which can be used in wound healing. BioMed Central 2021-01-07 /pmc/articles/PMC7792190/ /pubmed/33413682 http://dx.doi.org/10.1186/s13287-020-02106-7 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhao, Xiaohong Bian, Ruyu Wang, Fan Wang, Ying Li, Xue Guo, Yicheng Zhang, Xiaorong Luo, Gaoxing Zhan, Rixing GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling |
title | GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling |
title_full | GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling |
title_fullStr | GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling |
title_full_unstemmed | GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling |
title_short | GDF-5 promotes epidermal stem cells proliferation via Foxg1-cyclin D1 signaling |
title_sort | gdf-5 promotes epidermal stem cells proliferation via foxg1-cyclin d1 signaling |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792190/ https://www.ncbi.nlm.nih.gov/pubmed/33413682 http://dx.doi.org/10.1186/s13287-020-02106-7 |
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