Estradiol-17 beta (E-2) is suspected to exert a role in the regulation of t
esticular activity. Using a nonmammalian vertebrate model (the frog, Rana e
sculenta), we have investigated whether c-fos activity is detectable in the
testis during the annual sexual cycle and whether E-2 exerts a regulatory
role on spermatogenesis through fos activity. FOS protein is available in t
esticular nuclear extracts (about 60 kDa) and, surprisingly, also in cytoso
lic extracts (about 60, 80, and 100 kDa). Estradiol induces primary spermat
ogonia (ISPG) proliferation [this effect is counteracted by antiestrogens (
Tamoxifen and ICI 182-780)] and FOS appearance in testicular cytosolic extr
acts as well as c-fos transcription. Also, this effect is counteracted by I
CI 182-780. Interestingly, the number of FOS immunopositive nuclei of ISPG
strongly increases after E-2 treatment, whereas a great increase of immunop
ositivity in the cytoplasm of ISPG is observed with the contemporaneous tre
atment with antiestrogens.
In conclusion, our results demonstrate that E-2 induces ISPG multiplication
in the frog, R, esculenta, and, for the first time in a vertebrate species
, that it triggers c-fos activity in the testis. Moreover, E-2 may be invol
ved in mechanisms related to FOS transport in the nucleus of ISPG to induce
the mitotic activity.