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Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches

Gonadal white adipose tissue (gWAT) can regulate gametogenesis via modulation of neuroendocrine signaling. However, the effect of gWAT on the local microenvironment of the gonad was largely unknown. Herein, we ruled out that gWAT had a neuroendocrine effect on gonad function through a unilateral lip...

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Autores principales: Yang, Chao-Fan, Liu, Wen-Wen, Wang, Hai-Quan, Zhang, Jia-Le, Li, Kang, Diao, Zhen-Yu, Yue, Qiu-Ling, Yan, Gui-Jun, Li, Chao-Jun, Sun, Hai-Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052151/
https://www.ncbi.nlm.nih.gov/pubmed/35278432
http://dx.doi.org/10.1016/j.jbc.2022.101818
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author Yang, Chao-Fan
Liu, Wen-Wen
Wang, Hai-Quan
Zhang, Jia-Le
Li, Kang
Diao, Zhen-Yu
Yue, Qiu-Ling
Yan, Gui-Jun
Li, Chao-Jun
Sun, Hai-Xiang
author_facet Yang, Chao-Fan
Liu, Wen-Wen
Wang, Hai-Quan
Zhang, Jia-Le
Li, Kang
Diao, Zhen-Yu
Yue, Qiu-Ling
Yan, Gui-Jun
Li, Chao-Jun
Sun, Hai-Xiang
author_sort Yang, Chao-Fan
collection PubMed
description Gonadal white adipose tissue (gWAT) can regulate gametogenesis via modulation of neuroendocrine signaling. However, the effect of gWAT on the local microenvironment of the gonad was largely unknown. Herein, we ruled out that gWAT had a neuroendocrine effect on gonad function through a unilateral lipectomy strategy, in which cutting off epididymal white adipose tissue could reduce seminiferous tubule thickness and decrease sperm counts only in the adjacent testis and epididymis of the affected gonad. Consistent with the results in males, in females, ovary mass was similarly decreased by lipectomy. We determined that the defects in spermatogenesis were mainly caused by augmented apoptosis and decreased proliferation of germ cells. Transcriptome analysis suggested that lipectomy could disrupt immune privilege and activate immune responses in both the testis and ovary on the side of the lipectomy. In addition, lipidomics analysis in the testis showed that the levels of lipid metabolites such as free carnitine were elevated, whereas the levels of glycerophospholipids such as phosphatidylcholines and phosphatidylethanolamines were decreased, which indicated that the metabolic niche was also altered. Finally, we show that supplementation of phosphatidylcholine and phosphatidylethanolamine could partially rescue the observed phenotype. Collectively, our findings suggest that gWAT is important for gonad function by not only affecting whole-body homeostasis but also via maintaining local metabolic and immune niches.
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spelling pubmed-90521512022-05-03 Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches Yang, Chao-Fan Liu, Wen-Wen Wang, Hai-Quan Zhang, Jia-Le Li, Kang Diao, Zhen-Yu Yue, Qiu-Ling Yan, Gui-Jun Li, Chao-Jun Sun, Hai-Xiang J Biol Chem Research Article Gonadal white adipose tissue (gWAT) can regulate gametogenesis via modulation of neuroendocrine signaling. However, the effect of gWAT on the local microenvironment of the gonad was largely unknown. Herein, we ruled out that gWAT had a neuroendocrine effect on gonad function through a unilateral lipectomy strategy, in which cutting off epididymal white adipose tissue could reduce seminiferous tubule thickness and decrease sperm counts only in the adjacent testis and epididymis of the affected gonad. Consistent with the results in males, in females, ovary mass was similarly decreased by lipectomy. We determined that the defects in spermatogenesis were mainly caused by augmented apoptosis and decreased proliferation of germ cells. Transcriptome analysis suggested that lipectomy could disrupt immune privilege and activate immune responses in both the testis and ovary on the side of the lipectomy. In addition, lipidomics analysis in the testis showed that the levels of lipid metabolites such as free carnitine were elevated, whereas the levels of glycerophospholipids such as phosphatidylcholines and phosphatidylethanolamines were decreased, which indicated that the metabolic niche was also altered. Finally, we show that supplementation of phosphatidylcholine and phosphatidylethanolamine could partially rescue the observed phenotype. Collectively, our findings suggest that gWAT is important for gonad function by not only affecting whole-body homeostasis but also via maintaining local metabolic and immune niches. American Society for Biochemistry and Molecular Biology 2022-03-10 /pmc/articles/PMC9052151/ /pubmed/35278432 http://dx.doi.org/10.1016/j.jbc.2022.101818 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Yang, Chao-Fan
Liu, Wen-Wen
Wang, Hai-Quan
Zhang, Jia-Le
Li, Kang
Diao, Zhen-Yu
Yue, Qiu-Ling
Yan, Gui-Jun
Li, Chao-Jun
Sun, Hai-Xiang
Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
title Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
title_full Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
title_fullStr Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
title_full_unstemmed Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
title_short Gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
title_sort gonadal white adipose tissue is important for gametogenesis in mice through maintenance of local metabolic and immune niches
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052151/
https://www.ncbi.nlm.nih.gov/pubmed/35278432
http://dx.doi.org/10.1016/j.jbc.2022.101818
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