• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

卵巢储备的遗传学

Genetics of the ovarian reserve.

作者信息

Pelosi Emanuele, Forabosco Antonino, Schlessinger David

机构信息

Intramural Research Program, National Institute on Aging, National Institutes of Health , Baltimore, MD, USA.

Genomic Research Centre, Cante di Montevecchio Association , Fano, Italy.

出版信息

Front Genet. 2015 Oct 15;6:308. doi: 10.3389/fgene.2015.00308. eCollection 2015.

DOI:10.3389/fgene.2015.00308
PMID:26528328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4606124/
Abstract

Primordial follicles or non-growing follicles (NGFs) are the functional unit of reproduction, each comprising a single germ cell surrounded by supporting somatic cells. NGFs constitute the ovarian reserve (OR), prerequisite for germ cell ovulation and the continuation of the species. The dynamics of the reserve is determined by the number of NGFs formed and their complex subsequent fates. During the reproductive lifespan, the OR progressively diminishes due to follicle atresia as well as recruitment, maturation, and ovulation. The depletion of the OR is the major determining driver of menopause, which ensues when the number of primordial follicles falls below a threshold of ∼1,000. Therefore, genes and processes involved in follicle dynamics are particularly important to understand the process of menopause, both in the typical reproductive lifespan and in conditions like primary ovarian insufficiency, defined as menopause before age 40. Genes and their variants that affect the timing of menopause thereby provide candidates for diagnosis of and intervention in problems of reproductive lifespan. We review the current knowledge of processes and genes involved in the development of the OR and in the dynamics of ovarian follicles.

摘要

原始卵泡或静止卵泡(NGFs)是生殖的功能单位,每个原始卵泡都包含一个被支持性体细胞包围的单个生殖细胞。静止卵泡构成了卵巢储备(OR),这是生殖细胞排卵和物种延续的先决条件。卵巢储备的动态变化由形成的静止卵泡数量及其随后复杂的命运所决定。在生殖寿命期间,由于卵泡闭锁以及募集、成熟和排卵,卵巢储备会逐渐减少。卵巢储备的耗尽是绝经的主要决定性因素,当原始卵泡数量降至约1000个的阈值以下时就会发生绝经。因此,无论是在典型的生殖寿命期间,还是在原发性卵巢功能不全(定义为40岁之前绝经)等情况下,了解参与卵泡动态变化的基因和过程对于理解绝经过程尤为重要。影响绝经时间的基因及其变体为诊断和干预生殖寿命问题提供了候选对象。我们综述了目前关于参与卵巢储备发育和卵泡动态变化的过程及基因的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef30/4606124/b32c383d4dfc/fgene-06-00308-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef30/4606124/b32c383d4dfc/fgene-06-00308-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef30/4606124/b32c383d4dfc/fgene-06-00308-g0001.jpg

相似文献

1
Genetics of the ovarian reserve.卵巢储备的遗传学
Front Genet. 2015 Oct 15;6:308. doi: 10.3389/fgene.2015.00308. eCollection 2015.
2
Anti-Müllerian hormone: ovarian reserve testing and its potential clinical implications.抗缪勒管激素:卵巢储备检测及其潜在的临床意义。
Hum Reprod Update. 2014 Sep-Oct;20(5):688-701. doi: 10.1093/humupd/dmu020. Epub 2014 May 12.
3
AMH/MIS as a contraceptive that protects the ovarian reserve during chemotherapy.抗苗勒管激素/苗勒管抑制物质作为一种在化疗期间保护卵巢储备的避孕药。
Proc Natl Acad Sci U S A. 2017 Feb 28;114(9):E1688-E1697. doi: 10.1073/pnas.1620729114. Epub 2017 Jan 30.
4
Development of a Chemical Reproductive Aging Model in Female Rats.雌性大鼠化学性生殖衰老模型的建立。
Bio Protoc. 2021 Apr 20;11(8):e3994. doi: 10.21769/BioProtoc.3994.
5
Ovarian reserve assessment in users of oral contraception seeking fertility advice on their reproductive lifespan.口服避孕药使用者的卵巢储备评估,以寻求对其生殖寿命的生育建议。
Hum Reprod. 2015 Oct;30(10):2364-75. doi: 10.1093/humrep/dev197. Epub 2015 Aug 25.
6
[Reconsidering the roles of female germ cells in ovarian development and folliculogenesis].[重新审视雌性生殖细胞在卵巢发育和卵泡发生中的作用]
Biol Aujourdhui. 2011;205(4):223-33. doi: 10.1051/jbio/2011022. Epub 2012 Jan 19.
7
Changes in keratin 8/18 expression in human granulosa cell lineage are associated to cell death/survival events: potential implications for the maintenance of the ovarian reserve.角蛋白 8/18 表达的变化与人颗粒细胞系中的细胞死亡/存活事件有关:对维持卵巢储备的潜在影响。
Hum Reprod. 2018 Apr 1;33(4):680-689. doi: 10.1093/humrep/dey010.
8
Ovarian reserve and reproductive age may be determined from measurement of ovarian volume by transvaginal sonography.卵巢储备功能和生育年龄可通过经阴道超声测量卵巢体积来确定。
Hum Reprod. 2004 Jul;19(7):1612-7. doi: 10.1093/humrep/deh285. Epub 2004 Jun 17.
9
Dynamics of the ovarian reserve and impact of genetic and epidemiological factors on age of menopause.卵巢储备的动态变化以及遗传和流行病学因素对绝经年龄的影响。
Biol Reprod. 2015 May;92(5):130. doi: 10.1095/biolreprod.114.127381. Epub 2015 Apr 22.
10
Spatiotemporal changes in mechanical matrisome components of the human ovary from prepuberty to menopause.人类卵巢从青春期前到绝经期机械基质组件的时空变化。
Hum Reprod. 2020 Jun 1;35(6):1391-1410. doi: 10.1093/humrep/deaa100.

引用本文的文献

1
Gut microbiota: emerging biomarkers and potential therapeutics for premature ovarian failure.肠道微生物群:卵巢早衰的新兴生物标志物及潜在治疗方法
Front Microbiol. 2025 Jul 15;16:1606001. doi: 10.3389/fmicb.2025.1606001. eCollection 2025.
2
The assembly and activation of the PANoptosome promote porcine granulosa cell programmed cell death during follicular atresia.PANoptosome的组装和激活在卵泡闭锁过程中促进猪颗粒细胞程序性细胞死亡。
J Anim Sci Biotechnol. 2024 Nov 5;15(1):147. doi: 10.1186/s40104-024-01107-3.
3
BCORL1, POF1B, and USP9X copy number variation in women with idiopathic diminished ovarian reserve.

本文引用的文献

1
Mcl-1 is a key regulator of the ovarian reserve.髓细胞白血病-1蛋白(Mcl-1)是卵巢储备功能的关键调节因子。
Cell Death Dis. 2015 May 7;6(5):e1755. doi: 10.1038/cddis.2015.95.
2
Identification and Characterization of LHX8 DNA Binding Elements.LHX8 DNA结合元件的鉴定与表征
Dev Reprod. 2012 Dec;16(4):379-84. doi: 10.12717/DR.2012.16.4.379.
3
Dynamics of the ovarian reserve and impact of genetic and epidemiological factors on age of menopause.卵巢储备的动态变化以及遗传和流行病学因素对绝经年龄的影响。
BCORL1、POF1B 和 USP9X 拷贝数变异与特发性卵巢储备功能降低的女性。
J Assist Reprod Genet. 2024 Sep;41(9):2279-2288. doi: 10.1007/s10815-024-03185-8. Epub 2024 Jul 12.
4
An Update on Physiopathological Roles of Akt in the ReprodAKTive Mammalian Ovary.Akt在哺乳动物卵巢生殖中的生理病理作用的最新进展。
Life (Basel). 2024 Jun 2;14(6):722. doi: 10.3390/life14060722.
5
Primary oocytes with cellular senescence features are involved in ovarian aging in mice.具有细胞衰老特征的初级卵母细胞参与小鼠卵巢衰老过程。
Sci Rep. 2024 Jun 13;14(1):13606. doi: 10.1038/s41598-024-64441-6.
6
A Molecular Perspective and Role of NAD in Ovarian Aging.NAD 在卵巢衰老中的分子视角和作用。
Int J Mol Sci. 2024 Apr 25;25(9):4680. doi: 10.3390/ijms25094680.
7
Primary oocytes with cellular senescence features are involved in ovarian aging in mice.具有细胞衰老特征的初级卵母细胞参与小鼠卵巢衰老过程。
bioRxiv. 2024 Jan 9:2024.01.08.574768. doi: 10.1101/2024.01.08.574768.
8
FOXO3 and PTEN expression in the ovary of girls with extra-gonadal cancer with or without chemotherapy treatment prior to cryopreservation.在性腺外癌症女童的卵巢中,FOXO3和PTEN的表达情况,这些女童在卵巢冷冻保存之前接受或未接受化疗治疗。
BMC Womens Health. 2023 Sep 22;23(1):509. doi: 10.1186/s12905-023-02648-x.
9
Beyond apoptosis: evidence of other regulated cell death pathways in the ovary throughout development and life.超越细胞凋亡:在卵巢发育和生命过程中存在其他调控细胞死亡途径的证据。
Hum Reprod Update. 2023 Jul 5;29(4):434-456. doi: 10.1093/humupd/dmad005.
10
Factors influencing establishment of the ovarian reserve and their effects on fertility.影响卵巢储备建立的因素及其对生育能力的影响。
Anim Reprod. 2018 Aug 3;15(Suppl 1):635-647. doi: 10.21451/1984-3143-AR2018-0011. eCollection 2018 Jul-Sep.
Biol Reprod. 2015 May;92(5):130. doi: 10.1095/biolreprod.114.127381. Epub 2015 Apr 22.
4
MicroRNA-22-3p is down-regulated in the plasma of Han Chinese patients with premature ovarian failure.miRNA-22-3p 在汉族早发性卵巢功能衰竭患者血浆中表达下调。
Fertil Steril. 2015 Mar;103(3):802-7.e1. doi: 10.1016/j.fertnstert.2014.12.106. Epub 2015 Jan 10.
5
Committee opinion no. 618: Ovarian reserve testing.委员会意见第 618 号:卵巢储备测试。
Obstet Gynecol. 2015 Jan;125(1):268-273. doi: 10.1097/01.AOG.0000459864.68372.ec.
6
What is the "ovarian reserve"?什么是“卵巢储备功能”?
Fertil Steril. 2015 Mar;103(3):628-30. doi: 10.1016/j.fertnstert.2014.10.037. Epub 2014 Dec 12.
7
Oocyte ageing and epigenetics.卵母细胞衰老与表观遗传学。
Reproduction. 2015 Mar;149(3):R103-14. doi: 10.1530/REP-14-0242. Epub 2014 Nov 12.
8
BRCA1 germline mutations may be associated with reduced ovarian reserve.BRCA1基因种系突变可能与卵巢储备功能降低有关。
Fertil Steril. 2014 Dec;102(6):1723-8. doi: 10.1016/j.fertnstert.2014.08.014. Epub 2014 Sep 23.
9
Interleukin-1 deficiency prolongs ovarian lifespan in mice.白细胞介素-1缺乏可延长小鼠的卵巢寿命。
Proc Natl Acad Sci U S A. 2014 Aug 26;111(34):12492-7. doi: 10.1073/pnas.1323955111. Epub 2014 Aug 11.
10
Involvement of microRNA Mir15a in control of human ovarian granulosa cell proliferation, apoptosis, steroidogenesis, and response to FSH.微小RNA Mir15a参与对人卵巢颗粒细胞增殖、凋亡、类固醇生成及对促卵泡激素反应的调控。
Microrna. 2014;3(1):29-36. doi: 10.2174/2211536603666140227232824.