We investigated the androgen receptor (AR), metabolism and effects of
androgens in osteoblastic MC3T3-E1 cells. AR was proved as a transcrip
t of a IO-kb mRNA and as a 110-kDa protein. An immunocytochemical stud
y showed that AR was located mainly in the nuclei. Specific binding of
[H-3]DHT was observed in both the nuclear and cytosol fractions. MC3T
3-E1 cells possessed approximately 1190 binding sites per cell and mos
t of the sites (1150 sites) situated in the nucleus. The apparent K-d
value in the nuclear fraction was 1.35 nM for [H-3]DHT binding, and it
was similar to that for [H-3]testosterone. In the competition analysi
s, there was not much difference in the displacement of the [H-3] DHT
binding from AR between the addition of radioinert DHT and testosteron
e. In studies of 5 alpha-reductase activity and aromatase activity of
the cells, both activities were lower than the respective values in cl
assical androgen target tissues. Androgens stimulated the incorporatio
n of [H-3]thymidine into the cell, and DHT and testosterone had a simi
lar potency on the cell proliferation. Thus, these results suggest tes
tosterone itself acts mainly on the osteoblasts without conversion to
DHT.