To study transgene expression in the adult rat testis in vivo, an aden
ovirus vector carrying a lacZ transgene with a nuclear localization si
gnal was used as a marker. The adenovirus vector was first tested on r
at Sertoli cell-germ cell cocultures in vitro; it efficiently mediated
transgene expression in Sertoli cells but not germ cells. This vector
was then delivered to the interstitial compartment of adult rat teste
s by intratesticular injection, resulting in Leydig cells expressing t
he transgene. Alternatively, delivering the vector to the intratubular
compartment by rete testis injection resulted in expression of the tr
ansgene by Sertoli cells of the seminiferous epithelium and principal
cells of the epididymis. In vivo, each cell type expressed the transge
ne by 2 days postinfection, and expression persisted for at least 10 d
ays; however, later time points were associated with a loss of transge
ne expression and focal interstitial inflammation. This study document
s the ability of adenovirus to mediate gene transfer to specific testi
cular cells, providing a powerful tool to study the short-term effects
of specific genes on spermatogenesis in vivo.