Mediators of the biphasic responses of bone to intermittent and continuously administered parathyroid hormone

被引:159
作者
Locklin, RM
Khosla, S
Turner, RT
Riggs, BL
机构
[1] Mayo Clin & Mayo Fdn, Div Metab Endocrinol & Nutr, Endocrine Res Unit, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Orthoped, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
osteoblast differentiation; Runx2; insulin-like growth factor-1 (IGF-1); rank ligand; osteoprotegerin;
D O I
10.1002/jcb.10490
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
Parathyroid hormone (PTH) has biphasic effects on bone: continuous treatment is catabolic whereas intermittent treatment is anabolic. The mechanism(s) responsible for these differing effects are stil I unclear, partlybecause of the previous non-availability of a model system in which effects on both formation and resorption indices could be studied concomitantly. In cultured marrow cells from 6-week old C57BL/6 mice, we demonstrated that 4 days of intermittent PTH treatment increased mRNA for osteoblast differentiation markers(Runx2, alkaline phosphatase(AP), and type I procollagen (COL1A1) whereas continuous treatment resulted in production of large numbers of TRAP-positive multinucleated osteoclasts. Although IGF-I mRNA did not increase after intermittent treatment, it was consistently higher than after continuous treatment, and the addition of an anti-IGF-I neutralizing antibody prevented the increase in bone formation indices observed with intermittent treatment. By contrast, after continuous treatment, gene expression of RANK ligand (RANKL) was increased and that of osteoprotegerin (C)PG) was decreased, resulting in a 25-fold increase in the RANKL/OPG ratio. In this model system, the data suggest that intermittent PTH treatment enhances osteoblast differentiation through an IGF-I dependent mechanism and continuous PTH treatment enhances osteo.clastogenesis through reciprocal increases in RANKL and decreases in OPG. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:180 / 190
页数:11
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