Related Experiment Videos
Cell turnover in normal cycling human ovary
Y Funayama1, H Sasano, T Suzuki
1Department of Obstetrics and Gynecology, Tohoku University School of Medicine, Sendai, Japan.
The Journal of Clinical Endocrinology and Metabolism
|February 1, 1996
Summary
Cell proliferation, marked by Ki67 and PCNA, increases in human ovaries during early follicular development and in the functioning corpus luteum. Apoptosis was minimal, suggesting slow cell turnover in ovarian tissues.
Area of Science:
- Reproductive Biology
- Cellular Biology
- Gynecology
Background:
- Understanding cell turnover, including proliferation and apoptosis, is crucial for comprehending human ovarian function.
- The dynamic processes of follicular and luteal development involve complex cellular events that require detailed investigation.
Purpose of the Study:
- To investigate cell proliferation and apoptosis during various stages of human ovarian follicular and luteal development.
- To determine the significance of cell turnover in granulosa cells during folliculogenesis and luteogenesis.
Main Methods:
- Utilized immunostaining for Ki67 and PCNA to assess cell proliferation.
- Employed silver staining of nucleolar organizer regions (AgNORs) for proliferation assessment.
- Examined apoptosis using 3'-hydroxy nick-end labeling and Ley antigen immunostaining.
Main Results:
- Significantly increased labeling indexes for Ki67, PCNA, and AgNORs were observed in antral follicles.
- No significant differences in proliferation markers were found between dominant and nondominant follicles.
- Proliferation markers were predominantly observed in the functioning corpus luteum, not the degenerating corpus luteum.
- Apoptosis markers were rarely detected, except in scattered cells within the degenerating corpus luteum.
Conclusions:
- Granulosa cell transformation from quiescence to active growth is vital in early human folliculogenesis.
- Cell proliferation occurs during the luteal phase, specifically within the functioning corpus luteum.
- The low incidence of apoptosis suggests a slow process of follicular growth and atresia in human ovaries.