Levels of the hGSTM3 glutathione S-transferase (GST) subunit in testis
of the human fetus and infant were found to be only a small fraction
of those in adults. To understand these observations and to determine
whether hGSTM3 subunit expression is developmentally and/or hormonally
regulated, an experimental model based on the rat testis homologue (s
ubunit rGSTM5) was used. For prepubertal rats, testicular rGSTM5 subun
it levels were very low, but a sharp increase was observed between wee
ks 6 and 7 of development, when testicular growth includes increased n
umbers of germ cells associated with spermatogenesis. In adult hypophy
sectomized rats, the rGSTM5 subunit content of testis decreased progre
ssively over 5 weeks, at which time the subunit was barely detectable.
In contrast, the other GST subunit types did not vary significantly d
uring development or after hypophysectomy. These results suggest that
rGSTM5 subunits in rat testis could originate from spermatogenic cells
. Accordingly, GSTs were purified from human sperm, and it was shown t
hat the hGSTM3 subunit was, by a large measure, the predominant form.
These data are consistent with the notion that the differential expres
sion of hGSTM3 during human testicular development can also be explain
ed on the basis of its preferential location in germs cells.