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NELL-1 in the treatment of osteoporotic bone loss

机译:NELL-1治疗骨质疏松性骨丢失

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摘要

NELL-1 is a secreted, osteoinductive protein whose expression rheostatically controls skeletal ossification. Overexpression of NELL-1 results in craniosynostosis in humans and mice, whereas lack of Nell-1 expression is associated with skeletal undermineralization. Here we show that Nell-1-haploinsufficient mice have normal skeletal development but undergo age-related osteoporosis, characterized by a reduction in osteoblast: osteoclast (OB:OC) ratio and increased bone fragility. Recombinant NELL-1 binds to integrin beta 1 and consequently induces Wnt/b-catenin signalling, associated with increased OB differentiation and inhibition of OC-directed bone resorption. Systemic delivery of NELL-1 to mice with gonadectomy-induced osteoporosis results in improved bone mineral density. When extended to a large animal model, local delivery of NELL-1 to osteoporotic sheep spine leads to significant increase in bone formation. Altogether, these findings suggest that NELL-1 deficiency plays a role in osteoporosis and demonstrate the potential utility of NELL-1 as a combination anabolic/antiosteoclastic therapeutic for bone loss.
机译:NELL-1是一种分泌的骨诱导蛋白,其表达具有止血作用,可控制骨骼骨化。 NELL-1的过表达导致人和小鼠的颅骨前突,而Nell-1的表达缺乏与骨骼矿化不足有关。在这里,我们显示Nell-1-haploinsufficient小鼠具有正常的骨骼发育,但经历了与年龄有关的骨质疏松症,其特征是成骨细胞:破骨细胞(OB:OC)比例降低,骨骼脆弱性增加。重组NELL-1与整联蛋白beta 1结合,因此诱导Wnt / b-catenin信号传导,与增加的OB分化和抑制OC定向的骨吸收有关。向性腺切除术诱发的骨质疏松症小鼠全身递送NELL-1可改善骨矿物质密度。当扩展到大型动物模型时,将NELL-1局部递送至骨质疏松绵羊脊柱会导致骨形成显着增加。总而言之,这些发现表明,NELL-1缺乏症在骨质疏松症中起作用,并证明了NELL-1作为合成代谢/抗破骨细胞治疗骨丢失的组合的潜在用途。

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