New insights into osteoclastogenic signaling mechanisms

被引:284
作者
Nakashima, Tomoki [1 ,2 ]
Hayashi, Mikihito [1 ,2 ]
Takayanagi, Hiroshi [1 ,2 ,3 ]
机构
[1] Tokyo Med & Dent Univ, Dept Cell Signaling, Grad Sch Med & Dent Sci, Bunkyo Ku, Tokyo 1138549, Japan
[2] Japan Sci & Technol Agcy JST, Explorat Res Adv Technol ERATO Program, Takayanagi Osteonetwork Project, Bunkyo Ku, Tokyo 1138549, Japan
[3] Univ Tokyo, Dept Immunol, Grad Sch Med, Bunkyo Ku, Tokyo 1138549, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
KAPPA-B LIGAND; FAMILIAL EXPANSILE OSTEOLYSIS; LYMPH-NODE ORGANOGENESIS; NECROSIS-FACTOR RECEPTOR; DIFFERENTIATION FACTOR; RHEUMATOID-ARTHRITIS; BONE HOMEOSTASIS; OSTEOPROTEGERIN-LIGAND; T-CELLS; IDIOPATHIC HYPERPHOSPHATASIA;
D O I
10.1016/j.tem.2012.05.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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-kappa B 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.
引用
收藏
页码:582 / 590
页数:9
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