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Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells

BACKGROUND: A large number of autologous melanocytes are required for surgical treatment of depigmentation diseases such as vitiligo. The purpose of this experiment is to explore the application of melanocytes induced by mesenchymal stem cells to clinical treatment. Therefore, we have induced mouse...

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Autores principales: Xie, Yihui, Xu, Ziqian, Shi, Weimin, Mei, Xingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260302/
https://www.ncbi.nlm.nih.gov/pubmed/35844295
http://dx.doi.org/10.1016/j.reth.2022.06.007
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author Xie, Yihui
Xu, Ziqian
Shi, Weimin
Mei, Xingyu
author_facet Xie, Yihui
Xu, Ziqian
Shi, Weimin
Mei, Xingyu
author_sort Xie, Yihui
collection PubMed
description BACKGROUND: A large number of autologous melanocytes are required for surgical treatment of depigmentation diseases such as vitiligo. The purpose of this experiment is to explore the application of melanocytes induced by mesenchymal stem cells to clinical treatment. Therefore, we have induced mouse bone marrow mesenchymal stem cells (BMMSCs) into melanocytes (miMels) in the previous experiment. This experiment continues the previous experiment to further study the biological functions of miMels and their application in tissue engineering. METHODS: We examined whether miMels can produce active tyrosinase, melanin, and response to α-MSH. The ability of miMels to produce melanin to keratinocytes was tested by co-culture. By applying miMels to tissue-engineered skin, the survival and function of miMels on the surface of nude mice were verified. RESULTS: MiMels can produce active tyrosinase and melanin, and can pass melanin to the co-cultured keratinocytes. Under the stimulation of α-MSH, the active tyrosinase and melanin content of miMels increased. We tried to apply it to the establishment of tissue-engineered skin and obtained tissue-engineered skin containing miMels. Then we tried to transplant tissue-engineered skin on the back skin of nude mice and succeeded. The transplanted miMels survived in local tissues, synthesized active tyrosinase and melanin, and expressed the marker protein of melanocytes. CONCLUSION: In short, miMels can be used as a cell source for tissue engineering skin. MiMels not only have a typical melanocyte morphology but also have the same biological functions as normal melanocytes. What's more important is its successful application in mouse tissue-engineered experiments.
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spelling pubmed-92603022022-07-15 Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells Xie, Yihui Xu, Ziqian Shi, Weimin Mei, Xingyu Regen Ther Original Article BACKGROUND: A large number of autologous melanocytes are required for surgical treatment of depigmentation diseases such as vitiligo. The purpose of this experiment is to explore the application of melanocytes induced by mesenchymal stem cells to clinical treatment. Therefore, we have induced mouse bone marrow mesenchymal stem cells (BMMSCs) into melanocytes (miMels) in the previous experiment. This experiment continues the previous experiment to further study the biological functions of miMels and their application in tissue engineering. METHODS: We examined whether miMels can produce active tyrosinase, melanin, and response to α-MSH. The ability of miMels to produce melanin to keratinocytes was tested by co-culture. By applying miMels to tissue-engineered skin, the survival and function of miMels on the surface of nude mice were verified. RESULTS: MiMels can produce active tyrosinase and melanin, and can pass melanin to the co-cultured keratinocytes. Under the stimulation of α-MSH, the active tyrosinase and melanin content of miMels increased. We tried to apply it to the establishment of tissue-engineered skin and obtained tissue-engineered skin containing miMels. Then we tried to transplant tissue-engineered skin on the back skin of nude mice and succeeded. The transplanted miMels survived in local tissues, synthesized active tyrosinase and melanin, and expressed the marker protein of melanocytes. CONCLUSION: In short, miMels can be used as a cell source for tissue engineering skin. MiMels not only have a typical melanocyte morphology but also have the same biological functions as normal melanocytes. What's more important is its successful application in mouse tissue-engineered experiments. Japanese Society for Regenerative Medicine 2022-07-03 /pmc/articles/PMC9260302/ /pubmed/35844295 http://dx.doi.org/10.1016/j.reth.2022.06.007 Text en © 2022 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Xie, Yihui
Xu, Ziqian
Shi, Weimin
Mei, Xingyu
Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
title Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
title_full Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
title_fullStr Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
title_full_unstemmed Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
title_short Biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
title_sort biological function and application of melanocytes induced and transformed by mouse bone marrow mesenchymal stem cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260302/
https://www.ncbi.nlm.nih.gov/pubmed/35844295
http://dx.doi.org/10.1016/j.reth.2022.06.007
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