PTEN Expression in Human Granulosa Cells Is Associated with Ovarian Responses and Clinical Outcomes in IVF

Reprod Sci. 2021 Jul;28(7):1910-1921. doi: 10.1007/s43032-020-00429-7. Epub 2021 Jan 13.

Abstract

The ovarian reserve determines the success of in vitro fertilization (IVF) and embryo transfer treatment. It predicts the ovarian response in controlled ovarian hyperstimulation cycles. Apoptosis in granulosa cells surrounding oocytes is important for ovarian function and has been closely associated with follicular atresia. PTEN (encoding phosphatase and tensin homolog) is a well-known tumor suppressor gene that functions as a mediator of apoptosis and is crucial for mammal reproduction. In the present study, we analyzed the expression level of PTEN in human granulosa cells and aimed to investigate its association with the ovarian response and clinical outcomes in IVF. Apoptosis in granulosa cells were analyzed using Annexin V-Allophycocyanin staining after PTEN short hairpin RNA lentivirus transfection. Real-time fluorescent quantitative PCR analysis showed that the PTEN transcript level was significantly higher in poor responders and significantly lower in high responders, compared with that in normal responders. However, PTEN expression in the pregnancy group decreased slightly, but not significantly, compared with that in the non-pregnancy group. The apoptosis rate of granulosa cells declined significantly after 24-h transfection of the PTEN-shRNA lentivirus. These results suggest a fundamental role of PTEN in the regulation of follicular development, and that it might be involved in the pathogenesis of follicular dysplasia and ovarian dysfunction.

Keywords: Gene expression; Granulosa cells; Ovarian response; PTEN; Transfection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cumulus Cells / metabolism
  • Female
  • Fertilization in Vitro*
  • Granulosa Cells / metabolism*
  • Humans
  • Oocyte Retrieval
  • Oocytes / metabolism
  • Ovary / metabolism*
  • Ovulation Induction
  • PTEN Phosphohydrolase / metabolism*

Substances

  • PTEN Phosphohydrolase