SOST/sclerostin, an osteocyte-derived negative regulator of bone formation

被引:296
作者
Bezooijen, RL
ten Dijke, P
Papapoulos, SE
Löwik, CWGM
机构
[1] Leiden Univ, Med Ctr, Dept Endocrinol & Metab Dis, NL-2333 ZA Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2333 AL Leiden, Netherlands
关键词
SOST/sclerostin; sclerosteosis/Van Buchem disease; osteocyte; bone formation; BMP antagonist;
D O I
10.1016/j.cytogfr.2005.02.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Sclerosteosis and Van Buchem disease are two closely related bone disorders characterized by progressive bone thickening due to increased bone formation. Sclerosteosis is associated with mutations in the SOST gene and Van Buchem disease with a 52 kb deletion downstream of the SOST gene that probably affects transcription of the gene. Expression of the gene product sclerostin in bone is restricted to osteocytes and it is a negative regulator of bone formation. It inhibits BMP-stimulated bone formation, but cannot antagonize all BMP responses. The exclusive bone phenotype of good quality of patients with sclerosteosis and Van Buchem disease and the specific localization of sclerostin make it an attractive target for the development of bone forming therapeutics. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:319 / 327
页数:9
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