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Specialized Roles for Actin in Osteoclasts: Unanswered Questions and Therapeutic Opportunities

机译:肌动蛋白在破骨细胞中的特殊作用:悬而未决的问题和治疗机会

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Osteoclasts are cells of the hematopoietic lineage that are specialized to resorb bone. In osteoclasts, the actin cytoskeleton engages in at least two unusual activities that are required for resorption. First, microfilaments form a dynamic and structurally elaborate actin ring. Second, microfilaments bind vacuolar H + -ATPase (V-ATPase) and are involved in forming the V-ATPase-rich ruffled plasma membrane. The current review examines these two specialized functions with emphasis on the identification of new therapeutic opportunities. The actin ring is composed of substructures called podosomes that are interwoven to form a cohesive superstructure. Studies examining the regulation of the formation of actin rings and its constituent proteins are reviewed. Areas where there are gaps in the knowledge are highlighted. Microfilaments directly interact with the V-ATPase through an actin binding site in the B2-subunit of V-ATPase. This binding interaction is required for ruffled membrane formation. Recent studies show that an inhibitor of the interaction blocks bone resorption in pre-clinical animal models, including a model of post-menopausal osteoporosis. Because the unusual actin-based resorption complex is unique to osteoclasts and essential for bone resorption, it is likely that deeper understanding of its underlying mechanisms will lead to new approaches to treat bone disease.
机译:破骨细胞是专门用于吸收骨骼的造血谱系细胞。在破骨细胞中,肌动蛋白的细胞骨架至少参与了吸收所需的两种异常活动。首先,微丝形成动态且结构复杂的肌动蛋白环。其次,微丝结合液泡H + -ATPase(V-ATPase),并参与形成富含V-ATPase的皱纹质膜。当前的审查检查这两个专门功能,重点是确定新的治疗机会。肌动蛋白环由称为脚架的子结构组成,这些子结构交织形成内聚的上层结构。审查检查肌动蛋白环及其组成蛋白的形成的调节研究。突出知识差距的区域。微丝通过V-ATPase B2亚基中的肌动蛋白结合位点直接与V-ATPase相互作用。皱褶的膜形成需要这种结合相互作用。最近的研究表明,在临床前动物模型(包括绝经后骨质疏松症模型)中,这种相互作用的抑制剂会阻止骨吸收。由于不常见的基于肌动蛋白的吸收复合物是破骨细胞所特有的,并且是骨吸收所必需的,因此,对其潜在机制的更深入了解可能会导致治疗骨病的新方法。

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