Literature DB >> 18155187

Cryopreservation of ovarian tissues temporarily suppresses the proliferation of granulosa cells in mouse preantral follicles.

Jongyeob Choi1, Boeun Lee, Eunyoung Lee, Byung-Koo Yoon, Duksoo Bae, Dooseok Choi.   

Abstract

Cryopreservation of ovarian tissue has been reported to delay the development of preantral follicles during in vitro culture, but the mechanism causing this impairment has not been brought to light. In order to elucidate the underlying mechanism of delayed follicular development, we evaluated the effects of cryopreservation on the proliferation of granulosa cells during culture of mouse preantral follicles, as a sufficient population of granulosa cells is critical for normal follicular development. Additionally the initial cell death of granulosa cells was estimated immediately after cryopreservation. The ovarian tissues obtained from 12-day-old female mice were cryopreservation by vitrification. The granulosa cell proliferation was evaluated by measuring the PCNA expression and the expression of cell cycle regulators such as cyclin D2, CDK4, cyclin E and CDK2 in preantral follicles isolated from fresh and cryopreserved ovarian tissues that were cultured for 48 h. The viability of granulosa cells was evaluated by measuring the proportion of necrotic areas. The granulosa cell proliferation of the cryopreserved preantral follicles was decreased significantly compared to that of the fresh controls at 0 and 24h after culture (P<0.05), and this was increased to the control levels after 48 h of culture. The expressions of cyclin D2, Cdk4, cyclin E and Cdk2 were also decreased in the cryopreserved ovarian tissues at 0 and 24h after culture (P<0.05), but they were increased to the control levels after 48 h of culture. The proportion of the necrotic area was significantly higher in cryopreserved preantral follicles compared to that of the fresh preantral follicles (P<0.05). This suggests that cryopreservation of ovarian tissues may delay the preantral follicle development by temporary suppressing the granulosa cell proliferation through the cell cycle regulators (cyclin D2, Cdk4, cyclin E and Cdk2) and by granulosa cell death immediately after warming.

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Year:  2007        PMID: 18155187     DOI: 10.1016/j.cryobiol.2007.10.174

Source DB:  PubMed          Journal:  Cryobiology        ISSN: 0011-2240            Impact factor:   2.487


  5 in total

1.  Morphological and Molecular Aspects of In Vitro Culture of Preantral Follicles Derived from Vitrified Ovarian.

Authors:  Mahboobeh Amoushahi; Mojdeh Salehnia; Seyed Javad Mowla; Nassim Ghorbanmehr
Journal:  Cell J       Date:  2017-08-19       Impact factor: 2.479

2.  The Effects of Ovarian Encapsulation on Morphology and Expression of Apoptosis-Related Genes in Vitrified Mouse Ovary.

Authors:  Atefeh Shirazi Tehrani; Tahereh Mazoochi; Maryam Akhavan Taheri; Esmat Aghadavood; Mojdeh Salehnia
Journal:  J Reprod Infertil       Date:  2021 Jan-Mar

3.  Evaluating the Expression of Wnt Pathway Related Genes in Mouse Vitrified Preantral Follicles: An Experimental Study.

Authors:  Shahla Babaki; Saeed Zavareh; Parisa Farrokh; Meysam Nasiri
Journal:  J Reprod Infertil       Date:  2021 Jul-Sep

Review 4.  Cryopreservation/transplantation of ovarian tissue and in vitro maturation of follicles and oocytes: challenges for fertility preservation.

Authors:  Alex C Varghese; Stefan S du Plessis; Tommaso Falcone; Ashok Agarwal
Journal:  Reprod Biol Endocrinol       Date:  2008-10-02       Impact factor: 5.211

5.  Comparison of quartz vials with polypropylene vials for rapid cryopreservation of human ovarian tissue.

Authors:  D Scheiner; G Bracone; P Imesch; D Fink; J Hehl; B Imthurn
Journal:  J Ovarian Res       Date:  2016-09-26       Impact factor: 4.234

  5 in total

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