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Effect of Human Ovarian Tissue Vitrification/Warming on the Expression of Genes Related to Folliculogenesis
Authors:Zahra Shams Mofarahe  Marefat Ghaffari Novin  Mina Jafarabadi  Mojdeh Salehnia  Mohsen Noroozian  Nassim Ghorbanmehr
Affiliation:1.Dept. of Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; ;2.Reproductive Health Research Center, Tehran University of Medical Sciences, Tehran, Iran; ;3.Dept. of Anatomical Sciences, Tarbiat Modares University, Tehran, Iran; ;4.Biotechnology Group, Faculty of Biological Sciences, Alzahra University, Tehran , Iran
Abstract:

Background:

Ovarian tissue cryopreservation is an alternative strategy to preserve the fertility of women predicted to undergo premature ovarian failure. This study was designed to evaluate the expression of folliculogenesis-related genes, including factor in the germline alpha (FIGLA), growth differentiation factor-9 (GDF-9), follicle-stimulating hormone receptor (FSHR), and KIT LIGAND after vitrification/warming of human ovarian tissue.

Methods:

Human ovarian tissue samples were collected from five transsexual women. In the laboratory, the ovarian medullary part was removed by a surgical blade, and the cortical tissue was cut into small pieces. Some pieces were vitrified and warmed and the others were considered as non-vitrified group (control). Follicular normality was assessed with morphological observation by a light microscope, and the expression of FIGLA, KIT LIGAND, GDF-9,, and FSHR genes was examined using real-time RT-PCR in both the vitrified and non-vitrified groups.

Results:

Overall, 85% of the follicles preserved their normal morphologic feature after warming. The percentage of normal follicles and the expression of FIGLA, KIT LIGAND, GDF-9, and FSHR genes were similar in both vitrified and non-vitrified groups (P > 0.05).

Conclusion:

Vitrification/warming of human ovarian tissue had no remarkable effect on the expression of folliculogenesis-related genes. Key Words: Vitrification, Gene expression, Humans
Keywords:
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