Heparin fails to potentiate the effects of IL-1 beta-mediated bone resorption of fetal rat long bones in vitro

被引:5
作者
Panagakos, FS
Jandinski, JJ
Feder, L
Kumar, S
机构
[1] UNIV MED & DENT NEW JERSEY, NEW JERSEY DENT SCH, DEPT ORAL BIOL PATHOL & DIAGNOST SCI, NEWARK, NJ 07103 USA
[2] UNIV MED & DENT NEW JERSEY, NEW JERSEY MED SCH, DEPT BIOCHEM & MOLEC BIOL, NEWARK, NJ 07103 USA
关键词
heparin; bone resorption; interleukin-1; beta; cytokines;
D O I
10.1016/0300-9084(95)80001-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heparin has been identified as a potent modulator of bone resorption. Heparin induces osteoporosis during long-term administration and has been shown in vitro to enhance the effects of other bone resorbing factors, including parathyroid hormone. In this study, we examined the effects of heparin on the bone-resorbing activity of the inflammatory cytokine IL-1 beta. Resorption was determined by measuring release of previously incorporated Ca-45 from fetal rat long bones cultured in medium supplemented with either 0.1% bovine serum albumin or 10% heat-inactivated fetal calf serum. Heparin, in the absence of serum, decreased basal resorption at 4 and 10 units/ml, and slightly increased resorption at 30 units/ml. Heparin had no effect on IL-1 beta-stimulated resorption. In the presence of serum, heparin induced a two-fold increase in resorption alone, however, when cocultured with IL-1 beta, heparin failed to further enhance IL-1 beta-stimulated resorption.
引用
收藏
页码:915 / 918
页数:4
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