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Expression and regulation of RAB3 proteins in osteoclasts and their precursors.

机译:RAB3蛋白在破骨细胞及其前体中的表达和调控。

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The ruffled membrane, the resorptive organelle of the osteoclast, is generated by fusion of intracytoplasmic acidifying vesicles with the plasma membrane, an event analogous to regulated exocytosis. While the ruffled membrane is essential to the bone resorptive process, the mechanisms governing its generation are unknown. However, regulated exocytosis is mediated, in part, by isoforms of the Rab3 subset of Rab GTPases. Because of similarities between exocytosis and ruffled membrane formation, we asked if Rab3 proteins are expressed by osteoclasts or their precursors, and if so, are these molecules regulated by agents known to prompt the osteoclast phenotype? We find murine osteoclast precursors, in the form of bone marrow macrophages (BMMs), express at least two Rab3 isoforms, namely A and B/C, which are individually enhanced by a variety of hematopoietic cytokines. Consistent with the osteoclastogenic properties of a number of these cytokines, differentiation of BMMs into osteoclasts, in vitro, is associated with increased expression of both isoforms, particularly Rab3B/C. Finally, Rab3B/C localizes with the avian osteoclast H+ATPase (vacuolar proton pump) and pp60c-src, both intracellularly and within acidifying vesicles derived largely from the ruffled membrane. Thus, expression of specific rab3 proteins, an event which may control formation of the osteoclast ruffled membrane, is modulated by cytokines during osteoclastogenesis.
机译:皱纹膜是破骨细胞的吸收性细胞器,是通过胞质内酸化囊泡与质膜融合而产生的,这类似于调节的胞吐作用。尽管褶皱膜对于骨吸收过程至关重要,但控制其生成的机制尚不清楚。然而,调节的胞吐作用部分地由Rab GTPases的Rab3亚型的亚型介导。由于胞吐作用和褶皱膜形成之间的相似性,我们询问Rab3蛋白是否由破骨细胞或其前体表达,如果是,这些分子是否受促成破骨细胞表型的药剂调控?我们发现,小鼠破骨细胞前体以骨髓巨噬细胞(BMM)的形式表达至少两种Rab3亚型,即A和B / C,它们分别由多种造血细胞因子增强。与许多这些细胞因子的破骨细胞特性一致,BMM在体外分化为破骨细胞与两种同工型,尤其是Rab3B / C的表达增加有关。最终,Rab3B / C定位于禽破骨细胞H + ATPase(真空质子泵)和pp60c-src,在细胞内和酸化的囊泡中(主要来自褶皱的膜)。因此,在破骨细胞生成过程中,细胞因子调节特定的rab3蛋白的表达,该事件可能控制破骨细胞皱纹膜的形成。

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