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DYNAMICS OF THE ACTIN CYTOSKELETON IN OSTEOCLASTS

破骨细胞中肌动蛋白细胞骨架的动力学

基本信息

批准号：
7591685
负责人：
BETH S. LEE
金额：
$ 25.04万
依托单位：
OHIO STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2006
资助国家：
美国
起止时间：
2006-04-01 至 2011-03-31
项目状态：
已结题

项目摘要

Project Summary: Skeletal strength is achieved through a stringently controlled balance of bone formation and bone degradation. The cells responsible for this regulated degradation are osteoclasts, large multinucleated cells of the monocytic lineage. Osteoclasts undergo a cycle of activity that includes migration, polarization, bone resorption, and depolarization. These events require engagement of integrins and extensive rearrangements of the actin cytoskelton. Failure of osteoclasts to undergo these processes results in diminished cell function and potentially severe consequences to skeletal health such as osteopetrosis. The goal of this proposal is to examine the dynamics of the actin cytoskeleton in osteoclasts during events such as migration and polarization, and to understand the cellular elements required for this aspect of normal osteoclast function. The first aim of this proposal is directed toward the molecular motor myosin IIA, which is closely associatedwith dynamic actin structures involved in osteoclast migration and polarization. The potential functions of this motor will be assessed both by suppressing its activity and by following its trafficking in living cells. The goal of the second aim is directed toward understanding roles of other myosin isoforms in osteoclasts, particularly as they might pertain to cell signaling pathways. Finally, we have identified isoforms of tropomyosins with defined distributions in osteoclasts. Tropomyosins are filamentous proteins that can regulate the stability of actin, as well as its accessibility to other actin-binding proteins. We will examine the functions of these tropomyosins by alternately suppressing or enhancing their expression, and determining the effects on actin rearrangements in osteoclasts. These studies will provide new understanding of crucial processes mediated by the actin cytoskeleton in this dynamic cell type. Relevance: The ongoing process of bone formation and degradation must be kept in balance to maintain skeletal health. Bone degradation is performed by cells called osteoclasts, which depend on changes in their internal shape and structure for activity. The objective of this work is to understand some of the proteins that regulate the shape of osteoclasts, as part of a greater effort to comprehend how the activity of these cells is regulated.

项目概述：骨骼强度是通过严格控制骨形成的平衡来实现的和骨降解。负责这种调节性降解的细胞是破骨细胞，单核细胞系的多核细胞。破骨细胞经历一个活动周期，包括迁移、极化、骨吸收和去极化。这些事件需要整合素的参与和大量的肌动蛋白细胞因子重排。破骨细胞不能进行这些过程导致细胞功能减弱，并对骨骼健康造成潜在的严重后果，骨硬化症。这个建议的目的是检查动态的肌动蛋白细胞骨架在破骨细胞在迁移和极化等事件中，并了解其所需的细胞成分破骨细胞功能正常。这项建议的第一个目标是针对分子马达肌球蛋白IIA，与破骨细胞迁移中的动态肌动蛋白结构密切相关，极化该运动的潜在功能将通过抑制其活动和因为它贩卖活细胞第二个目标的目的是为了理解破骨细胞中的其他肌球蛋白亚型，特别是因为它们可能与细胞信号传导途径有关。最后，我们已经鉴定了在破骨细胞中具有确定分布的原肌球蛋白的同种型。原肌球蛋白是丝状蛋白，可以调节肌动蛋白的稳定性，以及其对其他肌动蛋白结合的可及性 proteins.我们将研究这些原肌球蛋白的功能，通过交替抑制或增强它们的功能，表达，并确定对破骨细胞中肌动蛋白重排的影响。这些研究将提供对这种动态细胞类型中由肌动蛋白细胞骨架介导的关键过程的新理解。相关性：骨形成和降解的持续过程必须保持平衡，骨骼健康骨降解是由称为破骨细胞的细胞完成的，破骨细胞依赖于骨细胞的变化。它们的内部形状和活动结构。这项工作的目的是了解一些调节破骨细胞形状的蛋白质，作为更大努力的一部分，以了解破骨细胞的活性是如何改变的。这些细胞受到调节。