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Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes

Background: To study the effect of allogeneic umbilical cord mesenchymal stem cell transplantation on the structure and function of the thymus in aged C57 mice and provide a new method for the treatment of senile thymic atrophy. Results: The changes in the thymus cortex and medulla volume and the ly...

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Autores principales: Pan, Xing-Hua, Lin, Qing-Keng, Yao, Xiang, Li, Zi-An, Cai, Xue-Min, Pang, Rong-Qing, Ruan, Guang-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521525/
https://www.ncbi.nlm.nih.gov/pubmed/32924972
http://dx.doi.org/10.18632/aging.103594
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author Pan, Xing-Hua
Lin, Qing-Keng
Yao, Xiang
Li, Zi-An
Cai, Xue-Min
Pang, Rong-Qing
Ruan, Guang-Ping
author_facet Pan, Xing-Hua
Lin, Qing-Keng
Yao, Xiang
Li, Zi-An
Cai, Xue-Min
Pang, Rong-Qing
Ruan, Guang-Ping
author_sort Pan, Xing-Hua
collection PubMed
description Background: To study the effect of allogeneic umbilical cord mesenchymal stem cell transplantation on the structure and function of the thymus in aged C57 mice and provide a new method for the treatment of senile thymic atrophy. Results: The changes in the thymus cortex and medulla volume and the lymphocyte ratio were analyzed by immunofluorescence. For thymus tissue sections, immunohistochemical staining was performed to detect p16, p53, SOD, becline1, LC3b, p62, sirt1, and sirt3. Changes in CK5, CK8, CD4 and CD8 expression were observed. Treatment with mUCMSCs could promote hair regeneration in aging mice and regenerate the thymus structure. Conclusions: mUCMSCs inhibited senescence of the thymus and promoted structural and functional thymus regeneration by downregulating the senescence genes p53 and p16 and upregulating the SOD, Sirt1 and Sirt3 genes, but the mechanism requires further research. Methods: C57 mice were obtained and met the requirements of thymic aging. mUCMSCs were infused via the tail vein at a dose of 1×10(7) cells/kg twice per week for 3 weeks. Six weeks after the last transplantation, the thymus was weighed, and the thymus-to-body weight ratio was calculated. The thymus tissue was stained with HE.
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spelling pubmed-75215252020-10-02 Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes Pan, Xing-Hua Lin, Qing-Keng Yao, Xiang Li, Zi-An Cai, Xue-Min Pang, Rong-Qing Ruan, Guang-Ping Aging (Albany NY) Research Paper Background: To study the effect of allogeneic umbilical cord mesenchymal stem cell transplantation on the structure and function of the thymus in aged C57 mice and provide a new method for the treatment of senile thymic atrophy. Results: The changes in the thymus cortex and medulla volume and the lymphocyte ratio were analyzed by immunofluorescence. For thymus tissue sections, immunohistochemical staining was performed to detect p16, p53, SOD, becline1, LC3b, p62, sirt1, and sirt3. Changes in CK5, CK8, CD4 and CD8 expression were observed. Treatment with mUCMSCs could promote hair regeneration in aging mice and regenerate the thymus structure. Conclusions: mUCMSCs inhibited senescence of the thymus and promoted structural and functional thymus regeneration by downregulating the senescence genes p53 and p16 and upregulating the SOD, Sirt1 and Sirt3 genes, but the mechanism requires further research. Methods: C57 mice were obtained and met the requirements of thymic aging. mUCMSCs were infused via the tail vein at a dose of 1×10(7) cells/kg twice per week for 3 weeks. Six weeks after the last transplantation, the thymus was weighed, and the thymus-to-body weight ratio was calculated. The thymus tissue was stained with HE. Impact Journals 2020-09-14 /pmc/articles/PMC7521525/ /pubmed/32924972 http://dx.doi.org/10.18632/aging.103594 Text en Copyright: © 2020 Pan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Pan, Xing-Hua
Lin, Qing-Keng
Yao, Xiang
Li, Zi-An
Cai, Xue-Min
Pang, Rong-Qing
Ruan, Guang-Ping
Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
title Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
title_full Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
title_fullStr Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
title_full_unstemmed Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
title_short Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
title_sort umbilical cord mesenchymal stem cells protect thymus structure and function in aged c57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521525/
https://www.ncbi.nlm.nih.gov/pubmed/32924972
http://dx.doi.org/10.18632/aging.103594
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