New regulation mechanisms of osteoclast differentiation

被引:107
作者
Nakashima, Tomoki [1 ,2 ]
Takayanagi, Hiroshi [1 ,3 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Cell Signal, Tokyo, Japan
[2] Japan Sci & Technol Agcy JST, Exploratory Res Adv Technol ERATO, Takayanagi Osteonetwork Project, Tokyo, Japan
[3] Global Ctr Excellence GCOE Program, Int Res Ctr Mol Sci Tooth & Bone Dis, Tokyo, Japan
来源
SKELETAL BIOLOGY AND MEDICINE II: BONE AND CARTILAGE HOMEOSTASIS AND BONE DISEASE | 2011年 / 1240卷
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
osteoimmunology; osteocyte; RANKL; NFATc1; KAPPA-B LIGAND; BONE HOMEOSTASIS; RECEPTOR ACTIVATOR; DEFECTIVE INTERLEUKIN-1; NUCLEAR-FACTOR; IMMUNE-SYSTEM; T-CELLS; RANKL; OSTEOPETROSIS; EXPRESSION;
D O I
10.1111/j.1749-6632.2011.06373.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoclasts play a crucial role in both physiological and pathological bone resorption. It is, thus, of compelling importance to understand the molecular mechanisms of osteoclast regulation. Because receptor activator of nuclear factor-kappa B ligand (RANKL) is the key cytokine that induces osteoclast differentiation, we have focused on the investigation of RANKL signaling and RANKL-expressing cells. Here, we summarize the recent advances in the understanding of osteoclastogenic signaling and the cells that express RANKL in the context of osteoimmunology. The scope of osteoimmunology has been extended to now encompass a wide range of molecular and cellular interactions, and its framework provides a scientific basis for future therapeutic approaches to diseases related to the bone and/or immune systems.
引用
收藏
页码:E13 / E18
页数:6
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