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Androgen stimulation of Sertoli cell function is enhanced by peritubular cells
Molecular and Cellular Endocrinology
|May 1, 1985
Summary
Testosterone partially prevents the decline in androgen binding protein (ABP) production by Sertoli cells. Peritubular cells and their secreted factors further support ABP production, suggesting a dual androgen action mechanism.
Area of Science:
- Reproductive biology
- Cellular and molecular endocrinology
- Spermatogenesis
Background:
- Sertoli cells are crucial for spermatogenesis, producing androgen binding protein (ABP).
- ABP levels are sensitive to hormonal and cellular microenvironment changes.
- Peritubular cells interact with Sertoli cells, influencing their function.
Purpose of the Study:
- To investigate the regulation of androgen binding protein (ABP) production by Sertoli cells.
- To determine the role of testosterone and peritubular cells in ABP synthesis.
- To elucidate the mechanisms by which peritubular cells influence Sertoli cell function.
Main Methods:
- Culture of purified Sertoli cell-enriched aggregates in serum-free minimal essential medium (MEM).
- Addition of testosterone or 17 beta-estradiol to the culture medium.
- Co-culture of Sertoli cells with peritubular cells or use of peritubular cell-conditioned medium.
- Measurement of androgen binding protein (ABP) production rates.
Main Results:
- ABP production rates declined in cultured Sertoli cell aggregates.
- Testosterone partially prevented this decline, while 17 beta-estradiol did not.
- The presence of peritubular cells enhanced the effect of testosterone on ABP production.
- Conditioned medium from peritubular cells sustained ABP production rates in Sertoli cell aggregates.
Conclusions:
- Peritubular cells, through secreted factors, modulate Sertoli cell ABP production.
- Androgens may act directly on Sertoli cells and indirectly via peritubular cells.
- This suggests a complex regulatory network involving androgens, Sertoli cells, and peritubular cells in regulating ABP synthesis.