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

Citation
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
Citations number
66
Categorie Soggetti
Cell Biology
ISSN journal
00219541
Volume
175
Issue
1
Year of publication
1998
Pages
78 - 88
Database
ISI
SICI code
0021-9541(1998)175:1<78:OPRIG(>2.0.ZU;2-X
Abstract
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.