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A bioenergetic shift is required for spermatogonial differentiation

A bioenergetic balance between glycolysis and mitochondrial respiration is particularly important for stem cell fate specification. It however remains to be determined whether undifferentiated spermatogonia switch their preference for bioenergy production during differentiation. In this study, we fo...

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Autores principales: Chen, Wei, Zhang, Zhaoran, Chang, Chingwen, Yang, Zhichang, Wang, Pengxiang, Fu, Haihui, Wei, Xiao, Chen, Eric, Tan, Suxu, Huang, Wen, Sun, Liangliang, Ni, Ting, Yang, Yi, Wang, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431567/
https://www.ncbi.nlm.nih.gov/pubmed/32864161
http://dx.doi.org/10.1038/s41421-020-0183-x
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author Chen, Wei
Zhang, Zhaoran
Chang, Chingwen
Yang, Zhichang
Wang, Pengxiang
Fu, Haihui
Wei, Xiao
Chen, Eric
Tan, Suxu
Huang, Wen
Sun, Liangliang
Ni, Ting
Yang, Yi
Wang, Yuan
author_facet Chen, Wei
Zhang, Zhaoran
Chang, Chingwen
Yang, Zhichang
Wang, Pengxiang
Fu, Haihui
Wei, Xiao
Chen, Eric
Tan, Suxu
Huang, Wen
Sun, Liangliang
Ni, Ting
Yang, Yi
Wang, Yuan
author_sort Chen, Wei
collection PubMed
description A bioenergetic balance between glycolysis and mitochondrial respiration is particularly important for stem cell fate specification. It however remains to be determined whether undifferentiated spermatogonia switch their preference for bioenergy production during differentiation. In this study, we found that ATP generation in spermatogonia was gradually increased upon retinoic acid (RA)-induced differentiation. To accommodate this elevated energy demand, RA signaling concomitantly switched ATP production in spermatogonia from glycolysis to mitochondrial respiration, accompanied by increased levels of reactive oxygen species. Disrupting mitochondrial respiration significantly blocked spermatogonial differentiation. Inhibition of glucose conversion to glucose-6-phosphate or pentose phosphate pathway also repressed the formation of c-Kit(+) differentiating germ cells, suggesting that metabolites produced from glycolysis are required for spermatogonial differentiation. We further demonstrated that the expression levels of several metabolic regulators and enzymes were significantly altered upon RA-induced differentiation, with both RNA-seq and quantitative proteomic analyses. Taken together, our data unveil a critically regulated bioenergetic balance between glycolysis and mitochondrial respiration that is required for spermatogonial proliferation and differentiation.
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spelling pubmed-74315672020-08-27 A bioenergetic shift is required for spermatogonial differentiation Chen, Wei Zhang, Zhaoran Chang, Chingwen Yang, Zhichang Wang, Pengxiang Fu, Haihui Wei, Xiao Chen, Eric Tan, Suxu Huang, Wen Sun, Liangliang Ni, Ting Yang, Yi Wang, Yuan Cell Discov Article A bioenergetic balance between glycolysis and mitochondrial respiration is particularly important for stem cell fate specification. It however remains to be determined whether undifferentiated spermatogonia switch their preference for bioenergy production during differentiation. In this study, we found that ATP generation in spermatogonia was gradually increased upon retinoic acid (RA)-induced differentiation. To accommodate this elevated energy demand, RA signaling concomitantly switched ATP production in spermatogonia from glycolysis to mitochondrial respiration, accompanied by increased levels of reactive oxygen species. Disrupting mitochondrial respiration significantly blocked spermatogonial differentiation. Inhibition of glucose conversion to glucose-6-phosphate or pentose phosphate pathway also repressed the formation of c-Kit(+) differentiating germ cells, suggesting that metabolites produced from glycolysis are required for spermatogonial differentiation. We further demonstrated that the expression levels of several metabolic regulators and enzymes were significantly altered upon RA-induced differentiation, with both RNA-seq and quantitative proteomic analyses. Taken together, our data unveil a critically regulated bioenergetic balance between glycolysis and mitochondrial respiration that is required for spermatogonial proliferation and differentiation. Springer Singapore 2020-08-18 /pmc/articles/PMC7431567/ /pubmed/32864161 http://dx.doi.org/10.1038/s41421-020-0183-x Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chen, Wei
Zhang, Zhaoran
Chang, Chingwen
Yang, Zhichang
Wang, Pengxiang
Fu, Haihui
Wei, Xiao
Chen, Eric
Tan, Suxu
Huang, Wen
Sun, Liangliang
Ni, Ting
Yang, Yi
Wang, Yuan
A bioenergetic shift is required for spermatogonial differentiation
title A bioenergetic shift is required for spermatogonial differentiation
title_full A bioenergetic shift is required for spermatogonial differentiation
title_fullStr A bioenergetic shift is required for spermatogonial differentiation
title_full_unstemmed A bioenergetic shift is required for spermatogonial differentiation
title_short A bioenergetic shift is required for spermatogonial differentiation
title_sort bioenergetic shift is required for spermatogonial differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431567/
https://www.ncbi.nlm.nih.gov/pubmed/32864161
http://dx.doi.org/10.1038/s41421-020-0183-x
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