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BOR - Papers in Press, published online ahead of print January 19, 2005.
Biol Reprod 2005, 10.1095/biolreprod.104.039321
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Submitted December 19, 2004
Returned for revision January 5, 2005
Accepted January 10, 2005

Testis


Follicle Stimulating Hormone Regulates Both Sertoli Cell and Spermatogonial Populations In the Adult Photoinhibited Djungarian Hamster Testis

Sarah J. Meachem *, Peter G. Stanton , and Stefan Schlatt

* To whom correspondence should be addressed. E-mail: sarah.meachem{at}phimr.monash.edu.au.

Abstract
The hormones that regulate spermatogonial development are ill defined, in part due to lack of appropriate experimental models. The photoinhibited hamster model provides a rich source of spermatogonia, thus making it an ideal model to study their control. This study aimed to assess the effects of FSH, in the absence of testosterone, on the re-initiation of Sertoli cell and spermatogonial development in the photosensitive adult Djungarian hamster. Hamsters raised under long photoperiods (LD, 16L:8D) were exposed to short photoperiods (SD, 8L:16D) for 11 weeks leading to suppression of gonadotropins and regression of testicular function. Groups of 10 animals then received FSH alone or in combination with the anti-androgen, flutamide for 7 days. Two control groups maintained either under long or short photoperiods were treated with vehicle. Sertoli and germ cell number were then determined using the optical dissector (sic) stereological technique. The number of Sertoli cells, type A spermatogonia, type B spermatogonia/preleptotene spermatocytes and leptotene/zygotene spermatocytes were suppressed in short day controls, to 66%, 34%, 19% and 10% (all P<0.01) of long day control values, respectively. Later germ cell types were not detected. FSH treatment, with or without flutamide, increased Sertoli cell number (P<0.01) to normal long day values. Similarly, FSH treatment in the absence/presence of flutamide increased type A spermatogonia, type B spermatogonia/preleptotene spermatocytes and leptotene/zygotene spermatocytes to ~85%, 69% and 80% (all P<0.01) of long day controls, respectively. Our data demonstrate that the re-initiation of spermatogonial maturation in this model is dependent on FSH, in the absence of androgens. Surprisingly the adult Sertoli cell population in this model is also hormone-dependent. This naturally occurring model provides a unique opportunity to understand the mechanisms (apoptotic and/or proliferative) by which FSH regulates Sertoli and germ cell development in the adult animal.

Key words: Testis • Follicle-stimulating hormone • Sertoli cells • Spermatogenesis


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