Literature DB >> 22301887

The primordial follicle reserve is not renewed after chemical or γ-irradiation mediated depletion.

J B Kerr1, L Brogan, M Myers, K J Hutt, T Mladenovska, S Ricardo, K Hamza, C L Scott, A Strasser, J K Findlay.   

Abstract

Reports indicate that germ-line stem cells present in adult mice can rapidly generate new oocytes and contribute to the primordial follicle reserve following conditions of ovotoxic stress. We further investigated the hypothesis that adult mice have the capacity to generate new oocytes by monitoring primordial follicle numbers throughout postnatal life and following depletion of the primordial follicle reserve by exposure to doxorubicin (DXR), trichostatin A (TSA), or whole-body γ-irradiation. We show that primordial follicle number remains stable in adult C57BL/6 mice between the ages of 25 and 100 days. However, within 2 days of treatment with DXR or TSA, primordial follicle numbers had declined to 65 and 51% respectively (P<0.05-0.01 when compared to untreated controls), with no restoration of follicle numbers evident after 7 days for either treatment. Furthermore, ovaries from mice subjected to sterilizing doses of γ-irradiation (0.45 or 4.5 Gy) revealed complete ablation of all primordial follicles 5 days after treatment, with no indication of follicular renewal. We conclude that neo-folliculogenesis does not occur following chemical or γ-irradiation mediated depletion of the primordial follicle reserve.

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Year:  2012        PMID: 22301887     DOI: 10.1530/REP-11-0430

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


  32 in total

1.  Experimental evidence showing that no mitotically active female germline progenitors exist in postnatal mouse ovaries.

Authors:  Hua Zhang; Wenjing Zheng; Yan Shen; Deepak Adhikari; Hiroo Ueno; Kui Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-09       Impact factor: 11.205

Review 2.  The developmental origins of the mammalian ovarian reserve.

Authors:  Kathryn J Grive; Richard N Freiman
Journal:  Development       Date:  2015-08-01       Impact factor: 6.868

3.  Female mice lack adult germ-line stem cells but sustain oogenesis using stable primordial follicles.

Authors:  Lei Lei; Allan C Spradling
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-29       Impact factor: 11.205

4.  Use of an organotypic mammalian in vitro follicle growth assay to facilitate female reproductive toxicity screening.

Authors:  Yuanming Xu; Francesca E Duncan; Min Xu; Teresa K Woodruff
Journal:  Reprod Fertil Dev       Date:  2015-02-18       Impact factor: 2.311

Review 5.  Cell-intrinsic reprogramming capability: gain or loss of pluripotency in germ cells.

Authors:  Masanori Imamura; Zachary Yu-Ching Lin; Hideyuki Okano
Journal:  Reprod Med Biol       Date:  2012-06-19

Review 6.  The capacity of oocytes for DNA repair.

Authors:  Jessica M Stringer; Amy Winship; Seng H Liew; Karla Hutt
Journal:  Cell Mol Life Sci       Date:  2018-05-10       Impact factor: 9.261

7.  Oocytes can efficiently repair DNA double-strand breaks to restore genetic integrity and protect offspring health.

Authors:  Jessica M Stringer; Amy Winship; Nadeen Zerafa; Matthew Wakefield; Karla Hutt
Journal:  Proc Natl Acad Sci U S A       Date:  2020-05-07       Impact factor: 11.205

8.  Role of p63 and the Notch pathway in cochlea development and sensorineural deafness.

Authors:  Alessandro Terrinoni; Valeria Serra; Ernesto Bruno; Andreas Strasser; Elizabeth Valente; Elsa R Flores; Hans van Bokhoven; Xin Lu; Richard A Knight; Gerry Melino
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-15       Impact factor: 11.205

9.  Rescue of platinum-damaged oocytes from programmed cell death through inactivation of the p53 family signaling network.

Authors:  S-Y Kim; M H Cordeiro; V A Serna; K Ebbert; L M Butler; S Sinha; A A Mills; T K Woodruff; T Kurita
Journal:  Cell Death Differ       Date:  2013-04-19       Impact factor: 15.828

10.  DNA damage-induced primordial follicle oocyte apoptosis and loss of fertility require TAp63-mediated induction of Puma and Noxa.

Authors:  Jeffrey B Kerr; Karla J Hutt; Ewa M Michalak; Michele Cook; Cassandra J Vandenberg; Seng H Liew; Philippe Bouillet; Alea Mills; Clare L Scott; Jock K Findlay; Andreas Strasser
Journal:  Mol Cell       Date:  2012-09-20       Impact factor: 17.970

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