Literature DB >> 24006465

Combating ovarian aging depends on the use of existing ovarian follicles, not on putative oogonial stem cells.

Hua Zhang1, Deepak Adhikari, Wenjing Zheng, Kui Liu.   

Abstract

Ovarian aging is characterized by both a reduction in egg quality and a drastic reduction in the number of ovarian follicles. It has been generally accepted for 60 years that a fixed population of primordial follicles is established in the ovaries during early life, and in most mammalian species, oocytes cannot renew themselves in postnatal or adult life. This dogma, however, has been challenged over the past decade. In this review, we summarize the recent studies on primordial follicles and putative oogonial stem cells and discuss what resources in the ovary might be more reliable and promising source tools for combating ovarian aging.

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Year:  2013        PMID: 24006465     DOI: 10.1530/REP-13-0202

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  3 in total

1.  Seeing is believing: no adult oogenesis in mammals.

Authors:  Hua Zhang; Kui Liu
Journal:  Cell Cycle       Date:  2015       Impact factor: 4.534

2.  microRNA 92b-3p regulates primordial follicle assembly by targeting TSC1 in neonatal mouse ovaries.

Authors:  Tingting Li; Xiaoqiu Liu; Xuefeng Gong; Qiukai E; Xiaoqian Zhang; Xuesen Zhang
Journal:  Cell Cycle       Date:  2019-04-06       Impact factor: 4.534

Review 3.  Mechanisms controlling germline cyst breakdown and primordial follicle formation.

Authors:  Chao Wang; Bo Zhou; Guoliang Xia
Journal:  Cell Mol Life Sci       Date:  2017-02-14       Impact factor: 9.261

  3 in total

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