Journal of Assisted Reproduction and Genetics

, Volume 23, Issue 4, pp 199–206 | Cite as

Maintenance of In Vitro Granulosa Cell Function by Adenoviral Mediated Follicle Stimulating Hormone Receptor Gene Transduction

  • Takehiro Serikawa
  • Kazuyuki Fujita
  • Hiroshi Nagata
  • Takashi Oite
  • Kenichi TanakaEmail author

Purpose: To maintain in vitro granulosa cell function by adenoviral-mediated FSHR gene transduction.

Methods: Rat granulosa cells were cultured and transduced with adenovirus carrying FSHR gene. The number of receptors and the rate of steroidogenesis were assessed.

Results: The number of FSHR on the granulosa cells was 4,874 per cell immediately after extraction, it was 2,176 by the third day, and had further reduced to 693 by the seventh day. On the third day of culture, the amount of production of estradiol by FSH stimulation also decreased to about one-quarter of the first day's quantity. Compared to the untransduced granulose cells, when the cells contained FSHR gene, the FSHR expression and steroidogenesis were both enhanced (2,176 vs. 7,206 per cell (p<0.001) and 192 vs. 5940 pg/mL (p<0.01), respectively).

Conclusion: Granulosa cell functions can be maintained or increased by novel gene therapy. This can be a useful component of assisted reproductive therapy.

Key Words:

Adenoviral vector FSH receptor granulosa cell in vitro maturation. 



We thank Dr. Toshihiro Takatoshi (Radioisotope Center, Niigata University), for variable suggestions for RRA. We also thank Dr. Alexander B. Olawaiye for his help in the final manuscript preparation. This study was supported in part by the Ministry of Education, Science, Sports and Culture of Japan to KF and KT.


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Copyright information

© Springer Science+Business Media, Inc. 2006

Authors and Affiliations

  • Takehiro Serikawa
    • 1
  • Kazuyuki Fujita
    • 1
  • Hiroshi Nagata
    • 1
  • Takashi Oite
    • 2
  • Kenichi Tanaka
    • 1
    • 3
    Email author
  1. 1.Department of Obstetrics and GynecologyGraduate School of Medical and Dental Sciences, Niigata UniversityNiigataJapan
  2. 2.Department of Cellular Physiology, Graduate School of Medical and Dental Sciences, Institute of NephrologyNiigata UniversityNiigataJapan
  3. 3.Graduate School of Medical and Dental SciencesNiigata UniversityNiigataJapan

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