The present study was undertaken to elucidate whether
estriol (E3) affects the proliferative activity and the expression of
insulin-like growth factor-I (
IGF-I)
mRNA and
IGF-I receptor (IGF-IR)
mRNA in cultured human osteoblast-like
osteosarcoma cells (HOS TE85). In this study, the effects of E3 on cultured HOS TE85 cells were compared with those of
17 beta-estradiol (E2). HOS TE85 cells were subcultured in
phenol red-free Dulbecco's modified Eagle's medium supplemented with 10%
fetal bovine serum for 72 h and then stepped down to serum-free conditions for an additional 72 h in the absence or presence of E3 (3.52 x 10(-9), 3.52 x 10(-8), 3.52 x 10(-7) mol/l) or E2 (3.67 x 10(-8) mol/l). Treatment with either E3 (3.52 x 10(-8), 3.52 x 10(-7) mol/l) or E2 (3.67 x 10(-8) mol/l) resulted in an increase in the number of cultured HOS TE85 cells and their uptake of
bromodeoxyuridine. Northern blot hybridization with a
IGF-I cDNA probe revealed that
RNA prepared from cultured HOS TE85 cells contained
IGF-I mRNA transcripts of 1.8, 4.4 and 7.5 kb. Treatment with either E3 (3.52 x 10(-9), 3.52 x 10(-8), 3.52 x 10(-7) mol/l) or E2 (3.67 x 10(-8) mol/l) resulted in increased expression of the three
mRNA transcripts relative tot hose in untreated control cultures. Semi-quantitative, reverse transcription polymerase chain reaction analysis showed that the 440-bp IGF-IR
mRNA transcript was present in HOS TE85 cells and that treatment with either E3 or E2 did not affect the IGF-IRmRNA expression in these cells. These results demonstrate that E3 (3.52 x 10(-9), 3.52 x 10(-8), 3.52 x 10(-7) mol/l) exerts profound effects on the proliferative potential of cultured HOS TE85 cells, compatible with that of E2 (3.67 x 10(-8) mol/l), through the induction of
IGF-I mRNA expression without affecting IGF-IR
mRNA expression in these cells.