Suppr超能文献

卵巢衰老的机制。

Mechanisms of ovarian aging.

机构信息

Department of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.

Department of Obstetrics, Gynecology, and Reproductive Sciences, Rutgers University Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.

出版信息

Reproduction. 2021 Jul 14;162(2):R19-R33. doi: 10.1530/REP-21-0022.

Abstract

Ovarian aging in women correlates with the progressive loss of both the number and quality of oocytes. When these processes occur early or are accelerated, their clinical correlates are diminished ovarian reserve and/or premature ovarian insufficiency. Both these conditions have important consequences for the reproductive and general health of women, including infertility. Although there are many contributing factors, the molecular mechanisms underlying many of the processes associated with ovarian aging have not been fully elucidated. In this review, we highlight some of the most critical factors that impact oocyte quantity and quality with advancing age. We discuss chromosomal factors including cohesion deterioration and mis-segregation, errors in meiotic recombination, and decreased stringency of the spindle assembly checkpoint. DNA damage, telomere changes, reactive oxygen species and mitochondrial dysfunction as they relate to ovarian aging, and well-known gene mutations associated with primary ovarian insufficiency and diminished ovarian reserve are also discussed. Additionally, studies investigating recently acknowledged cytoplasmic factors associated with ovarian aging including protein metabolic dysregulation and microenvironmental alterations in the ovary are presented. We use both mouse and human studies to support the roles these factors play in physiologic and expedited ovarian aging, and we propose directions for future studies. A better understanding of the molecular basis of ovarian aging will ultimately lead to diagnostic and therapeutic advancements that would provide women with information to make earlier choices about their reproductive health.

摘要

女性的卵巢衰老与卵母细胞数量和质量的逐渐丧失有关。当这些过程发生得较早或加速时,其临床相关表现为卵巢储备功能减退和/或卵巢早衰。这两种情况都会对女性的生殖和整体健康产生重要影响,包括不孕。尽管有许多促成因素,但许多与卵巢衰老相关的过程的分子机制尚未完全阐明。在这篇综述中,我们强调了一些随着年龄增长影响卵母细胞数量和质量的最关键因素。我们讨论了染色体因素,包括着丝粒的恶化和错误分离、减数分裂重组的错误以及纺锤体组装检查点的严格性降低。我们还讨论了与卵巢衰老相关的 DNA 损伤、端粒变化、活性氧和线粒体功能障碍以及与原发性卵巢功能不全和卵巢储备功能减退相关的已知基因突变。此外,还介绍了最近研究发现的与卵巢衰老相关的细胞质因素,包括蛋白质代谢失调和卵巢微环境改变。我们使用小鼠和人类研究来支持这些因素在生理和加速卵巢衰老中的作用,并提出了未来研究的方向。更好地理解卵巢衰老的分子基础最终将导致诊断和治疗的进步,为女性提供有关生殖健康的早期选择的信息。

相似文献

1
Mechanisms of ovarian aging.
Reproduction. 2021 Jul 14;162(2):R19-R33. doi: 10.1530/REP-21-0022.
2
Ovarian aging: mechanisms and intervention strategies.
Med Rev (2021). 2022 Nov 22;2(6):590-610. doi: 10.1515/mr-2022-0031. eCollection 2022 Dec.
3
Resveratrol protects against age-associated infertility in mice.
Hum Reprod. 2013 Mar;28(3):707-17. doi: 10.1093/humrep/des437. Epub 2013 Jan 4.
4
BRCA-related ATM-mediated DNA double-strand break repair and ovarian aging.
Hum Reprod Update. 2020 Jan 1;26(1):43-57. doi: 10.1093/humupd/dmz043.
5
Ovarian Aging in Women With BRCA Germline Mutations.
J Clin Endocrinol Metab. 2017 Oct 1;102(10):3839-3847. doi: 10.1210/jc.2017-00765.
6
Ovarian ageing: the role of mitochondria in oocytes and follicles.
Hum Reprod Update. 2016 Nov;22(6):725-743. doi: 10.1093/humupd/dmw028. Epub 2016 Aug 25.
7
CHTF18 ensures the quantity and quality of the ovarian reserve†.
Biol Reprod. 2020 Jun 23;103(1):24-35. doi: 10.1093/biolre/ioaa036.
8
Diminished ovarian reserve versus ovarian aging: overlaps and differences.
Curr Opin Obstet Gynecol. 2019 Jun;31(3):139-147. doi: 10.1097/GCO.0000000000000536.
9
Telomere dynamics and reproduction.
Fertil Steril. 2024 Jan;121(1):4-11. doi: 10.1016/j.fertnstert.2023.11.012. Epub 2023 Nov 21.
10
The Aging Ovary and the Tales Learned Since Fetal Development.
Sex Dev. 2023;17(2-3):156-168. doi: 10.1159/000532072. Epub 2023 Aug 18.

引用本文的文献

2
Environmental heavy metal exposure and altering anti-Mullerian hormone levels in women.
BMC Womens Health. 2025 Aug 23;25(1):404. doi: 10.1186/s12905-025-03952-4.
3
Mitochondrial dysfunction in oocytes: implications for fertility and ageing.
J Ovarian Res. 2025 Aug 14;18(1):186. doi: 10.1186/s13048-025-01764-6.
4
Reconstructing the female reproductive system using 3D bioprinting in tissue engineering.
Mater Today Bio. 2025 Jul 22;34:102127. doi: 10.1016/j.mtbio.2025.102127. eCollection 2025 Oct.
5
Mesenchymal Stem Cells: A Therapeutic Approach in Fertility Restoration in Premature Ovarian Insufficiency.
Stem Cell Rev Rep. 2025 Oct;21(7):2089-2102. doi: 10.1007/s12015-025-10944-2. Epub 2025 Aug 1.
6
The Right to Freeze Oocyte for Women in Iranian Fertility Centers: A Qualitative Study.
Med J Islam Repub Iran. 2025 Mar 5;39:35. doi: 10.47176/mjiri.39.35. eCollection 2025.
7
Ovarian aging, cardiovascular risk and inflammation: insights from the OVA study.
J Ovarian Res. 2025 Jul 26;18(1):164. doi: 10.1186/s13048-025-01754-8.
8
Role of cellular prion protein in mouse granulosa cells and its effects on ovarian function in knockout mice.
Mol Med Rep. 2025 Oct;32(4). doi: 10.3892/mmr.2025.13630. Epub 2025 Jul 25.
10
Aging Alters mRNA Processing in the Mouse Ovary.
Cells. 2025 Jun 30;14(13):996. doi: 10.3390/cells14130996.

本文引用的文献

1
The Inflammasome Contributes to Depletion of the Ovarian Reserve During Aging in Mice.
Front Cell Dev Biol. 2021 Feb 11;8:628473. doi: 10.3389/fcell.2020.628473. eCollection 2020.
2
Evaluation of inflammation and follicle depletion during ovarian ageing in mice.
Sci Rep. 2021 Jan 11;11(1):278. doi: 10.1038/s41598-020-79488-4.
3
Macrophage-derived multinucleated giant cells: hallmarks of the aging ovary.
Reproduction. 2021 Feb;161(2):V5-V9. doi: 10.1530/REP-20-0489.
4
The midlife transition and the risk of cardiovascular disease and cancer Part I: magnitude and mechanisms.
Am J Obstet Gynecol. 2020 Dec;223(6):820-833. doi: 10.1016/j.ajog.2020.05.051. Epub 2020 Jun 1.
5
Oocyte Elimination Through DNA Damage Signaling from CHK1/CHK2 to p53 and p63.
Genetics. 2020 Jun;215(2):373-378. doi: 10.1534/genetics.120.303182. Epub 2020 Apr 9.
6
CHTF18 ensures the quantity and quality of the ovarian reserve†.
Biol Reprod. 2020 Jun 23;103(1):24-35. doi: 10.1093/biolre/ioaa036.
8
Mitochondria as a biomarker for IVF outcome.
Reproduction. 2019 Jun;157(6):R235-R242. doi: 10.1530/REP-18-0580.
9
Segregating Chromosomes in the Mammalian Oocyte.
Curr Biol. 2018 Aug 20;28(16):R895-R907. doi: 10.1016/j.cub.2018.06.057.
10
Embryonal mitochondrial DNA: relationship to embryo quality and transfer outcomes.
J Assist Reprod Genet. 2018 May;35(5):871-877. doi: 10.1007/s10815-018-1147-z. Epub 2018 Mar 5.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验