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[破骨细胞的细胞生物学与骨吸收的分子机制]

[Cell biology of osteoclasts and molecular mechanisms of bone resorption].

作者信息

Amling M, Delling G

机构信息

Departments of Orthopedics and Cell Biology, Yale University, New Haven, Connecticut, USA.

出版信息

Pathologe. 1996 Sep;17(5):358-67. doi: 10.1007/s002920050173.

Abstract

The maintenance of a normal skeletal shape and bone mass closely depends on a normal osteoclastic activity, as do bone growth and repair. Thus, the improvement of our means of therapeutic intervention will depend on our better understanding of the molecular basis of bone resorption and of the cellbiology of the osteoclast. This review-article presents our current opinion of the molecular mechanisms of bone resorption by the osteoclast. After describing the morphological features of the osteoclast, aspects as cell mobility, attachment, enzymesynthesis, transmembrane transport, osteoclast differentiation and function, as well as the protooncogenes c-src and c-cbl and their role for bone resorption are presented in detail.

摘要

正常骨骼形状和骨量的维持密切依赖于正常的破骨细胞活性,骨骼生长和修复也是如此。因此,我们治疗干预手段的改进将取决于我们对骨吸收分子基础和破骨细胞细胞生物学的更好理解。这篇综述文章阐述了我们目前对破骨细胞骨吸收分子机制的看法。在描述了破骨细胞的形态特征后,详细介绍了细胞移动性、附着、酶合成、跨膜运输、破骨细胞分化和功能等方面,以及原癌基因c-src和c-cbl及其在骨吸收中的作用。

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