Skip Navigation


Mol. Hum. Reprod. Advance Access originally published online on January 19, 2009
Molecular Human Reproduction 2009 15(3):155-164; doi:10.1093/molehr/gap002
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
15/3/155    most recent
gap002v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Mazoochi, T.
Right arrow Articles by Hajizadeh, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mazoochi, T.
Right arrow Articles by Hajizadeh, E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Analysis of apoptosis and expression of genes related to apoptosis in cultures of follicles derived from vitrified and non-vitrified ovaries

Tahereh Mazoochi1, Mojdeh Salehnia1,5, Shahram Pourbeiranvand1, Mehdi Forouzandeh2, Seyed Javad Mowla3 and Ebrahim Hajizadeh4

1Department of Anatomy, Tarbiat Modares University, Tehran, Iran 2Department of Biotechnology, Tarbiat Modares University, Tehran, Iran 3Department of Genetic, Tarbiat Modares University, Tehran, Iran 4Department of Biostatistic, Tarbiat Modares University, Tehran, Iran

5 Corresponding author. Department of Anatomy, Tarbiat Modares University, PO Box 14115-111, Tehran, Iran. Tel: +98-21-88011001; Fax: +98-21-88013030; E-mail: mogdeh{at}dr.com, salehnim{at}modares.ac.ir

The aim of this study was to evaluate the incidence of apoptosis after in vitro culture of isolated follicles derived from vitrified and non-vitrified ovaries. Mouse ovaries were vitrified and their pre-antral follicles were mechanically isolated and cultured for 10 days. Growth and survival rates of the follicles were assessed during the culture period and the ultrastructure of the follicles was studied. The expression of p53, Bcl-2, Bax, Fas, FasL and survivin were analyzed by real-time RT–PCR in different follicular developmental stages. The percentages of apoptotic and necrotic cells were determined using a fluorescein-activated cell sorting (FACS) technique. There were no differences between the growth and survival rates of follicles in the vitrified and non-vitrified groups. All of the evaluated genes were expressed in the pre-antral, large pre-antral and antral follicles in both groups, except Fas mRNA, which was not expressed in the pre-antral follicles. The expression of p53, Bcl2, Bax and FasL mRNA was similar in vitrified and non-vitrified groups; however, Fas mRNAs were more strongly expressed in the antral follicles of the vitrified group than of the control group (P < 0.05). The expression of survivin 140 was lower in the antral follicles of the vitrified group than of the control group (P < 0.05). FACS analysis showed that the percentage of intact cells was lower in the vitrified group than in the non-vitrified group (P < 0.05). This study demonstrated no signs of apoptosis ultrastructurally in cultured follicles; however, vitrification was shown to affect the expression of some genes related to apoptosis.

Key words: Apoptosis/Gene expression/Follicular development/In vitro maturation/Vitrification

Submitted on May 26, 2008; resubmitted on December 27, 2008; accepted on January 14, 2009.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.