Advances in osteoclast differentiation and function.

Yousef Abu-Amer
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引用次数: 29

Abstract

Osteoclasts are the sole bone resorbing cells. These cells are essential for skeletal development and remodeling throughout the life of animal and man. Deficiency of osteoclasts leads to osteopetrosis, a diseases manifested by increased non-remodeled bone mass, which ultimately leads to bone deformities and functional failure of other body systems. On the other hand, increased number and activity of osteoclasts under certain pathologic conditions causes accelerated bone resorption and may lead to osteoporosis and osteolytic diseases. To better understand the mechanisms underlying osteoclast-based diseases and design relevant therapies, one should unveil the molecular basis of osteoclast differentiation and function and regulatory mechanisms of osteoclast signaling. This review will outline up-to-date information regarding osteoclast differentiation and activation. Molecular mechanisms underlying osteoclast signaling pathways in inflammatory osteolysis and arthritis will be discussed. In addition, stimulators and inhibitors of osteoclasts, as well as current therapies for osteoclast activity will be addressed.

破骨细胞分化与功能研究进展。
破骨细胞是唯一的骨吸收细胞。这些细胞在动物和人类的一生中对骨骼的发育和重塑至关重要。破骨细胞缺乏导致骨质疏松症,这种疾病表现为非重塑骨量增加,最终导致骨畸形和其他身体系统功能衰竭。另一方面,在某些病理条件下,破骨细胞数量和活性的增加导致骨吸收加速,并可能导致骨质疏松和溶骨疾病。为了更好地理解以破骨细胞为基础的疾病的机制和设计相关的治疗方法,我们应该揭示破骨细胞分化和功能的分子基础以及破骨细胞信号传导的调节机制。这篇综述将概述有关破骨细胞分化和激活的最新信息。在炎性骨溶解和关节炎中破骨细胞信号通路的分子机制将被讨论。此外,将讨论破骨细胞的刺激剂和抑制剂,以及目前的破骨细胞活性治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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