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成骨细胞与 WNT:骨形成的力学调控

Osteocytes and WNT: the mechanical control of bone formation.

机构信息

Unit of Periodontology, University of Parma, Via Gramsci 14, 43100 Parma, Italy.

出版信息

J Dent Res. 2010 Apr;89(4):331-43. doi: 10.1177/0022034510363963. Epub 2010 Mar 3.

Abstract

Mechanical loading is of pivotal importance in the maintenance of skeletal homeostasis, but the players involved in the transduction of mechanical stimuli to promote bone maintenance have long remained elusive. Osteocytes, the most abundant cells in bone, possess mechanosensing appendices stretching through a system of bone canaliculi. Mechanical stimulation plays an important role in osteocyte survival and hence in the preservation of bone mechanical properties, through the maintenance of bone hydratation. Osteocytes can also control the osteoblastic differentiation of mesenchymal precursors in response to mechanical loading by modulating WNT signaling pathways, essential regulators of cell fate and commitment, through the protein sclerostin. Mutations of Sost, the sclerostin-encoding gene, have dramatic effects on the skeleton, indicating that osteocytes may act as master regulators of bone formation and localized bone remodeling. Moreover, the development of sclerostin inhibitors is opening new possibilities for bone regeneration in orthopedics and the dental field.

摘要

机械加载对于维持骨骼内稳态至关重要,但长期以来,将机械刺激转化为促进骨骼维持的信号的参与者一直难以捉摸。成骨细胞是骨骼中最丰富的细胞,它们拥有延伸穿过骨小管系统的机械感受附属物。机械刺激通过维持骨骼水合作用,在成骨细胞存活和骨力学性能的维持中发挥重要作用。成骨细胞还可以通过调节 WNT 信号通路来控制间充质前体细胞的成骨细胞分化,WNT 信号通路是细胞命运和分化的重要调节剂,通过蛋白硬化素实现。Sost 基因(编码硬化素的基因)的突变对骨骼有显著影响,表明成骨细胞可能作为骨形成和局部骨重塑的主控调节因子。此外,硬化素抑制剂的开发为骨科和牙科领域的骨再生开辟了新的可能性。

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