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破骨细胞生成信号机制的新见解。

New insights into osteoclastogenic signaling mechanisms.

机构信息

Department of Cell Signaling, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Yushima 1-5-45, Bunkyo-ku, Tokyo 113-8549, Japan.

出版信息

Trends Endocrinol Metab. 2012 Nov;23(11):582-90. doi: 10.1016/j.tem.2012.05.005. Epub 2012 Jun 15.

Abstract

Bone is continuously renewed through a dynamic balance between bone resorption and formation. This process is the fundamental basis for the maintenance of normal bone mass and architecture. Osteoclasts play a crucial role in both physiological and pathological bone resorption, and receptor activator of nuclear factor-κB ligand (RANKL) is the key cytokine that induces osteoclastogenesis. Here we summarize the recent advances in the understanding of osteoclastogenic signaling by focusing on the investigation of RANKL signaling and RANKL-expressing cells in the context of osteoimmunology. The context afforded by osteoimmunology will provide a scientific basis for future therapeutic approaches to diseases related to the skeletal and immune systems.

摘要

骨骼通过骨吸收和形成之间的动态平衡不断更新。这个过程是维持正常骨量和结构的基础。破骨细胞在生理和病理骨吸收中都起着至关重要的作用,核因子-κB 配体受体激活剂(RANKL)是诱导破骨细胞生成的关键细胞因子。在这里,我们通过关注在骨免疫学背景下 RANKL 信号和 RANKL 表达细胞的研究,总结了对破骨细胞生成信号的最新理解进展。骨免疫学提供的背景将为未来与骨骼和免疫系统相关疾病的治疗方法提供科学依据。

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