Primate sperm acquire functional maturity, including vigorous forward motil
ity and the ability to fertilize an ovum, as they transit the unique, regio
nal microenvironment of the epididymal lumen. Several proteins secreted int
o this luminal fluid are epididymal-specific and androgen-dependent, and th
us contribute potentially to sperm maturation. For the adult male chimpanze
e, we report the effects of GnRH antagonist-induced androgen deprivation on
the histology of the epithelia and interstitium composing the ductuli effe
rentes, ductus epididymis, proximal ductus (vas) deferens. After 21 days of
androgen deprivation, epididymal tissues exhibit characteristic atrophic c
hanges, including cellular disorganization, degradation, and loss of struct
ures. Androgen-deprived cytoplasm is differentially and characteristically
disrupted, vacuolated, and reduced in volume, resulting in decreased epithe
lial height and loss of stereocilia. Most principal cell nuclei appear hype
rchromatic, smaller in size, more irregular in outline, and disordered in a
rrangement, while others appear swollen and vacuolated. Apical cells of the
efferent ducts and the basal cells and microvillar borders of the ductus e
pididymis seem minimally affected by androgen deprivation. Such histologica
lly differential responses suggest correspondingly that androgen is differe
ntially essential to the maintenance of the epididymis and thus to normal f
unctioning of the component tissues. Therefore, epididymal epithelia direct
ly and their secretions indirectly are differentially androgen-dependent. (
C) 2001 Harcourt Publishers Ltd.