Insulin at 3-100 nM increased the steady state level of α-l(I) procollagen mRNA and stimulated collagen synthesis in the osteoblast-rich segment of central bone from 21- day-old fetal rat calvaria. The increases in the level of procollagen mRNA and the rate of collagen synthesis were observed 18 h after the addition of insulin to the cultures. The removal of insulin from calvaria incubated for 24 h with 3 nM insulin caused collagen synthesis and the level of α-1(1) procollagen mRNA to return to control values within 5 h. Adding insulin back to calvaria withdrawn from insulin treatment for 3 h did not rescue the decay in collagen synthesis or the level of α-1(1) procollagen mRNA. Insulin increased the steady state levels of α-l(I) procollagen mRNA in the presence of the RNA synthesis inhibitor actinomycin-D. Our data suggest that in fetal rat bone, one mechanism by which insulin increases the steady state level of α-l(I) procollagen mRNA may be by altering its stability.
|Original language||English (US)|
|Number of pages||7|
|State||Published - Sep 1989|
ASJC Scopus subject areas