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The emerging role of lysine succinylation in ovarian aging

BACKGROUND: Ovarian aging is a process of decline in its reserve leading to ovary dysfunction and even reduced health quality in offspring. However, aging-related molecular pathways in the ovary remain obscure. Lysine succinylation (Ksuc), a newly post-translational modification (PTM), has been foun...

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Autores principales: Le, Meiling, Li, Jia, Zhang, Dalei, Yuan, Yuan, Zhou, Chong, He, Jinxia, Huang, Jian, Hu, Liaoliao, Luo, Tao, Zheng, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116721/
https://www.ncbi.nlm.nih.gov/pubmed/37081483
http://dx.doi.org/10.1186/s12958-023-01088-4
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author Le, Meiling
Li, Jia
Zhang, Dalei
Yuan, Yuan
Zhou, Chong
He, Jinxia
Huang, Jian
Hu, Liaoliao
Luo, Tao
Zheng, Liping
author_facet Le, Meiling
Li, Jia
Zhang, Dalei
Yuan, Yuan
Zhou, Chong
He, Jinxia
Huang, Jian
Hu, Liaoliao
Luo, Tao
Zheng, Liping
author_sort Le, Meiling
collection PubMed
description BACKGROUND: Ovarian aging is a process of decline in its reserve leading to ovary dysfunction and even reduced health quality in offspring. However, aging-related molecular pathways in the ovary remain obscure. Lysine succinylation (Ksuc), a newly post-translational modification (PTM), has been found to be broadly conserved in both eukaryotic and prokaryotic cells, and associated with multiple pathophysiological processes. There are no relevant reports revealing a link between the molecular mechanisms of ovarian aging and Ksuc. METHODS: The level of Ksuc in ovaries of aged and premature ovarian insufficiency (POI) mice were detected by immunoblotting and immunohistochemical. To further explore the role of Ksuc in ovarian aging, using in vitro mouse ovary tissue culture and an in vivo mouse model with changed Ksuc level. RESULTS: Increased Ksuc in ovaries of aged and POI mice and distribution of Ksuc in various types of mice ovarian cells and the high level of Ksuc in granulosa cells (GCs) were revealed. Histological assessments and hormone levels analyses showed that the high Ksuc level down-regulated the ovarian index and the anti-Müllerian hormone (AMH) and estrogen levels, and increased follicular atresia. Moreover, in the high Ksuc groups, the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) intensities and the expression of Cleaved-caspase-3 increased and the expression of B-cell lymphoma-2 (Bcl-2) decreased together with positively-expressed P21, an aging-related marker. These results suggest that ovarian aging is likely associated with alteration in Ksuc. CONCLUSION: The present study has identified Ksuc in mouse ovary and found that high Ksuc level most likely contributes to ovarian aging which is expected further investigation to provide new information for delaying physiological ovarian aging and treating pathological ovarian aging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12958-023-01088-4.
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spelling pubmed-101167212023-04-21 The emerging role of lysine succinylation in ovarian aging Le, Meiling Li, Jia Zhang, Dalei Yuan, Yuan Zhou, Chong He, Jinxia Huang, Jian Hu, Liaoliao Luo, Tao Zheng, Liping Reprod Biol Endocrinol Research BACKGROUND: Ovarian aging is a process of decline in its reserve leading to ovary dysfunction and even reduced health quality in offspring. However, aging-related molecular pathways in the ovary remain obscure. Lysine succinylation (Ksuc), a newly post-translational modification (PTM), has been found to be broadly conserved in both eukaryotic and prokaryotic cells, and associated with multiple pathophysiological processes. There are no relevant reports revealing a link between the molecular mechanisms of ovarian aging and Ksuc. METHODS: The level of Ksuc in ovaries of aged and premature ovarian insufficiency (POI) mice were detected by immunoblotting and immunohistochemical. To further explore the role of Ksuc in ovarian aging, using in vitro mouse ovary tissue culture and an in vivo mouse model with changed Ksuc level. RESULTS: Increased Ksuc in ovaries of aged and POI mice and distribution of Ksuc in various types of mice ovarian cells and the high level of Ksuc in granulosa cells (GCs) were revealed. Histological assessments and hormone levels analyses showed that the high Ksuc level down-regulated the ovarian index and the anti-Müllerian hormone (AMH) and estrogen levels, and increased follicular atresia. Moreover, in the high Ksuc groups, the terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) intensities and the expression of Cleaved-caspase-3 increased and the expression of B-cell lymphoma-2 (Bcl-2) decreased together with positively-expressed P21, an aging-related marker. These results suggest that ovarian aging is likely associated with alteration in Ksuc. CONCLUSION: The present study has identified Ksuc in mouse ovary and found that high Ksuc level most likely contributes to ovarian aging which is expected further investigation to provide new information for delaying physiological ovarian aging and treating pathological ovarian aging. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12958-023-01088-4. BioMed Central 2023-04-20 /pmc/articles/PMC10116721/ /pubmed/37081483 http://dx.doi.org/10.1186/s12958-023-01088-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Le, Meiling
Li, Jia
Zhang, Dalei
Yuan, Yuan
Zhou, Chong
He, Jinxia
Huang, Jian
Hu, Liaoliao
Luo, Tao
Zheng, Liping
The emerging role of lysine succinylation in ovarian aging
title The emerging role of lysine succinylation in ovarian aging
title_full The emerging role of lysine succinylation in ovarian aging
title_fullStr The emerging role of lysine succinylation in ovarian aging
title_full_unstemmed The emerging role of lysine succinylation in ovarian aging
title_short The emerging role of lysine succinylation in ovarian aging
title_sort emerging role of lysine succinylation in ovarian aging
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116721/
https://www.ncbi.nlm.nih.gov/pubmed/37081483
http://dx.doi.org/10.1186/s12958-023-01088-4
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