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Brown adipose tissue-derived exosomes delay fertility decline in aging mice

INTRODUCTION: Ovarian aging has steadily grown to be a significant health issue for women as a result of the increase in average life expectancy and the postponement of reproductive age. One of the important pathological foundations of ovarian aging is formed by mitochondrial dysfunction, which caus...

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Autores principales: Zhang, Hanke, Fang, Yuqing, Gao, Ying, Zeng, Xinliu, Lu, Zhenzhen, Liu, Lin, Chen, Chunyan, Huang, Jiayu, Li, Yanhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248460/
https://www.ncbi.nlm.nih.gov/pubmed/37305038
http://dx.doi.org/10.3389/fendo.2023.1180104
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author Zhang, Hanke
Fang, Yuqing
Gao, Ying
Zeng, Xinliu
Lu, Zhenzhen
Liu, Lin
Chen, Chunyan
Huang, Jiayu
Li, Yanhui
author_facet Zhang, Hanke
Fang, Yuqing
Gao, Ying
Zeng, Xinliu
Lu, Zhenzhen
Liu, Lin
Chen, Chunyan
Huang, Jiayu
Li, Yanhui
author_sort Zhang, Hanke
collection PubMed
description INTRODUCTION: Ovarian aging has steadily grown to be a significant health issue for women as a result of the increase in average life expectancy and the postponement of reproductive age. One of the important pathological foundations of ovarian aging is formed by mitochondrial dysfunction, which causes decreases in follicle quantity and oocyte quality. In recent years, brown adipose tissue (BAT) transplantation has been proven as an effective treatment for aging-related diseases, such as ovarian aging. However, BAT transplantation is an invasive operation with long-term risks. Therefore, we need to find an alternative strategy. METHODS: We injected BAT-derived exosomes into eight-month-old C57BL/6 female mice. The fertility was detected by the estrous cycle and mating test. The changes of ovary and oocyte were measured by ovarian volume, organ coefficient, follicle counting, and oocyte maturation rate. ROS level, mitochondrial membrane potential and ATP level were measured to analyze the mitochondrial function of oocytes. The changes in metabolism were explored by cold stimulation test, body weight and blood sugar. The possible molecular mechanism was further investigated by RNA sequencing. RESULTS: In terms of fertility, the estrous cycle of aging mice after BAT-derived exosome intervention was more regular, and the number of progenies and litters was increased. At the tissue level, the ovaries in the BAT-exosome group were larger, and the number of primordial follicles, secondary follicles, antral follicles and total follicles increased. At the cellular level, BAT-derived exosomes improved the maturation of oocytes in vivo and in vitro, increased the mitochondrial membrane potential and ATP levels of oocytes, and decreased ROS levels. Besides, BAT-derived exosomes ameliorated the metabolism and viability of aging mice. Furthermore, mRNA sequencing showed that BAT exosomes altered the expression levels of genes related to metabolism and the quality of oocytes. CONCLUSION: BAT-derived exosomes enhanced mitochondrial function, promoted follicle survival, improved fertility, and extended ovarian lifespan in aging mice.
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spelling pubmed-102484602023-06-09 Brown adipose tissue-derived exosomes delay fertility decline in aging mice Zhang, Hanke Fang, Yuqing Gao, Ying Zeng, Xinliu Lu, Zhenzhen Liu, Lin Chen, Chunyan Huang, Jiayu Li, Yanhui Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: Ovarian aging has steadily grown to be a significant health issue for women as a result of the increase in average life expectancy and the postponement of reproductive age. One of the important pathological foundations of ovarian aging is formed by mitochondrial dysfunction, which causes decreases in follicle quantity and oocyte quality. In recent years, brown adipose tissue (BAT) transplantation has been proven as an effective treatment for aging-related diseases, such as ovarian aging. However, BAT transplantation is an invasive operation with long-term risks. Therefore, we need to find an alternative strategy. METHODS: We injected BAT-derived exosomes into eight-month-old C57BL/6 female mice. The fertility was detected by the estrous cycle and mating test. The changes of ovary and oocyte were measured by ovarian volume, organ coefficient, follicle counting, and oocyte maturation rate. ROS level, mitochondrial membrane potential and ATP level were measured to analyze the mitochondrial function of oocytes. The changes in metabolism were explored by cold stimulation test, body weight and blood sugar. The possible molecular mechanism was further investigated by RNA sequencing. RESULTS: In terms of fertility, the estrous cycle of aging mice after BAT-derived exosome intervention was more regular, and the number of progenies and litters was increased. At the tissue level, the ovaries in the BAT-exosome group were larger, and the number of primordial follicles, secondary follicles, antral follicles and total follicles increased. At the cellular level, BAT-derived exosomes improved the maturation of oocytes in vivo and in vitro, increased the mitochondrial membrane potential and ATP levels of oocytes, and decreased ROS levels. Besides, BAT-derived exosomes ameliorated the metabolism and viability of aging mice. Furthermore, mRNA sequencing showed that BAT exosomes altered the expression levels of genes related to metabolism and the quality of oocytes. CONCLUSION: BAT-derived exosomes enhanced mitochondrial function, promoted follicle survival, improved fertility, and extended ovarian lifespan in aging mice. Frontiers Media S.A. 2023-05-25 /pmc/articles/PMC10248460/ /pubmed/37305038 http://dx.doi.org/10.3389/fendo.2023.1180104 Text en Copyright © 2023 Zhang, Fang, Gao, Zeng, Lu, Liu, Chen, Huang and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Zhang, Hanke
Fang, Yuqing
Gao, Ying
Zeng, Xinliu
Lu, Zhenzhen
Liu, Lin
Chen, Chunyan
Huang, Jiayu
Li, Yanhui
Brown adipose tissue-derived exosomes delay fertility decline in aging mice
title Brown adipose tissue-derived exosomes delay fertility decline in aging mice
title_full Brown adipose tissue-derived exosomes delay fertility decline in aging mice
title_fullStr Brown adipose tissue-derived exosomes delay fertility decline in aging mice
title_full_unstemmed Brown adipose tissue-derived exosomes delay fertility decline in aging mice
title_short Brown adipose tissue-derived exosomes delay fertility decline in aging mice
title_sort brown adipose tissue-derived exosomes delay fertility decline in aging mice
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248460/
https://www.ncbi.nlm.nih.gov/pubmed/37305038
http://dx.doi.org/10.3389/fendo.2023.1180104
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