OSTEOGENIC PROTEIN-1 REGULATES INSULIN-LIKE GROWTH-FACTOR-I (IGF-I), IGF-II, AND IGF-BINDING PROTEIN-5 (IGFBP-5) GENE-EXPRESSION IN FETAL-RAT CALVARIA CELLS BY DIFFERENT MECHANISMS
Lcc. Yeh et al., OSTEOGENIC PROTEIN-1 REGULATES INSULIN-LIKE GROWTH-FACTOR-I (IGF-I), IGF-II, AND IGF-BINDING PROTEIN-5 (IGFBP-5) GENE-EXPRESSION IN FETAL-RAT CALVARIA CELLS BY DIFFERENT MECHANISMS, Journal of cellular physiology, 175(1), 1998, pp. 78-88
Osteogenic protein-1 (OP-1 or BMP-7) stimulates new bone formation in
vivo and induces cell proliferation and differentiation of osteoblasts
in vitro. Previous studies from our laboratory revealed that OP-1 led
to a two-to threefold increase in steady-state insulin-like growth fa
ctor-I (IGF-I) and ICF-II mRNA levels and a fivefold decrease in IGF-b
inding protein-5 (IGFBP-5) mRNA levels in primary cultures of fetal ra
t calvaria (FRC) cells. In the present study, we determined whether th
e effects of OP-1 were at the transcriptional or posttranscriptional l
evel. OP-1 increased the half-life of the IGF-I mRNA from 6 to 17 h wi
thout changing the level of IGF-I nuclear pre-mRNA. In transiently tra
nsfected FRC cells, the luciferase activity driven by the -1122/+362 o
r the -133/+362 IGF-I exon 1 promoter fragment was not changed by OP-1
. Similar results were observed using the -1500/+44 or -362/+44 IGF-I
exon 2 promoter constructs. Effects of OP-1 on IGF-I mRNA were indepen
dent of cell division, as they remained elevated in the presence of hy
droxyurea. Cycloheximide inhibited moderately the OP-1-induced increas
e in IGF-I mRNA, suggesting partial dependency on protein synthesis. O
n the other hand, the IGF-II nuclear pre-mRNA levels were increased by
OP-1 but the half-life of the mature IGF-II mRNA was not affected. Ef
fects of, OP-1 on IGF-II mRNA were also independent of cell division,
but were dependent on protein synthesis. OP-1 caused a 43-50% reductio
n in the level of IGFBP-5 nuclear pre-mRNA transcripts and a 40% decre
ase in the IGFBP-5 promoter activity in FRC cells transfected with the
-1278/+1 IGFBP-5 promoter fragment. The half-life of the mature IGFBP
-5 mRNA was not affected by OP-1. Hydroxyurea did not prevent the OP-1
-induced reduction in IGFBP-5 mRNA. The level of IGFBP-5 mRNA was bare
ly detectable in the presence of cycloheximide, and further suppressiv
e effect of OP-1 on IGFBP-5 mRNA could not be determined. In conclusio
n, OP-1 regulates IGF-I gene expression at the posttranscriptional lev
el, but regulates IGF-II and IGFBP-5 gene expression at the transcript
ional level. (C) 1998 Wiley-Liss, Inc.