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c-Src激酶在破骨细胞功能调节中的作用。

The role of c-Src kinase in the regulation of osteoclast function.

作者信息

Miyazaki Tsuyoshi, Tanaka Sakae, Sanjay Archana, Baron Roland

机构信息

Department of Orthopaedic Surgery, Tokyo Metropolitan Komagome Hospital, 3-18-22 Komagome, Bunkyo-ku, Tokyo, 113-8677, Japan.

出版信息

Mod Rheumatol. 2006;16(2):68-74. doi: 10.1007/s10165-006-0460-z.

Abstract

The targeted disruption of c-Src impairs osteoclast bone resorbing activity, causing osteopetrosis. Although it has been reported that restoring only the c-Src adaptor function at least partly rescues the skeletal phenotypes, the importance of c-Src kinase activity remains controversial. We here highlight the contributions of the Src adaptor and kinase activities in cytoskeletal organization and osteoclast function using adenovirus vectors containing various mutants of Src or Pyk2. In addition, we describe the importance of c-Src in mitochondria, where it phosphorylates cytochrome c oxidase (Cox). Src-induced Cox activity is also required for bone resorbing activity of osteoclasts that require high levels of ATP. Thus, c-Src kinase activity not only on the plasma membrane but also within mitochondria is essential for the regulation of osteoclastic bone resorption.

摘要

c-Src的靶向破坏会损害破骨细胞的骨吸收活性,导致骨质石化。尽管有报道称仅恢复c-Src衔接蛋白功能至少可部分挽救骨骼表型,但c-Src激酶活性的重要性仍存在争议。我们在此利用含有Src或Pyk2各种突变体的腺病毒载体,强调Src衔接蛋白和激酶活性在细胞骨架组织和破骨细胞功能中的作用。此外,我们描述了c-Src在线粒体中的重要性,它在线粒体中使细胞色素c氧化酶(Cox)磷酸化。Src诱导的Cox活性对于需要高水平ATP的破骨细胞的骨吸收活性也是必需的。因此,c-Src激酶活性不仅在质膜上而且在线粒体内对于破骨细胞性骨吸收的调节都是必不可少的。

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