Endocrine functions of sclerostin

Ryan C. Riddle
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引用次数: 2

Abstract

Sclerostin, the product of the SOST gene has primarily been studied for its profound impact on bone mass. By interacting with LRP5 and LRP6, the glycoprotein suppresses the propagation of Wnt signals to β-catenin and thereby suppresses new bone formation. In this review, we discuss emerging data which suggest that sclerostin also acts outside the skeleton to influence metabolism. In humans, serum sclerostin levels are associated with body mass index and indices of metabolic function. Likewise, genetic mouse models of Sost gene deficiency indicate sclerostin influences adipocyte development and insulin signaling. These data raise the possibility that sclerostin neutralization may be effective at treating two epidemic conditions: osteoporosis and obesity.

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硬化素的内分泌功能
硬核蛋白是SOST基因的产物,主要研究其对骨量的深远影响。通过与LRP5和LRP6相互作用,糖蛋白抑制Wnt信号向β-连环蛋白的传播,从而抑制新骨的形成。在这篇综述中,我们讨论了新出现的数据,这些数据表明硬化素也在骨骼外发挥作用,影响新陈代谢。在人类中,血清硬化素水平与体重指数和代谢功能指数有关。同样,Sost基因缺乏的遗传小鼠模型表明,硬化素影响脂肪细胞发育和胰岛素信号传导。这些数据增加了硬化素中和可能有效治疗两种流行病的可能性:骨质疏松症和肥胖。
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来源期刊
Current Opinion in Endocrine and Metabolic Research
Current Opinion in Endocrine and Metabolic Research Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
4.10
自引率
0.00%
发文量
80
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