Emerging molecules in the interface between skeletal system and innate immunity

被引:8
作者
Maruyama, Kenta [1 ,2 ]
Akira, Shizuo [1 ,2 ,3 ]
机构
[1] Osaka Univ, Host Def Lab, Suita, Osaka 5650871, Japan
[2] Osaka Univ, WPI Immunol Frontier Res Ctr IFReC, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
基金
日本学术振兴会;
关键词
Osteoclast; Osteoblast; Neutrophil; Macrophage; Innate immunity; Bone destruction; NF-KAPPA-B; OSTEOCLASTOGENESIS-INHIBITORY FACTOR; JUN DIMERIZATION PROTEIN-2; TRANSCRIPTION FACTOR JDP2; LYMPH-NODE ORGANOGENESIS; CELL-CELL FUSION; BONE HOMEOSTASIS; DC-STAMP; C-FOS; DEFECTIVE INTERLEUKIN-1;
D O I
10.1016/j.phrs.2015.06.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the improved treatment of bone destruction, significant unmet medical need remains. For example, there is a limited benefit of continued bisphosphonate therapy for osteoporotic patients, and only minor populations of rheumatoid arthritis patients obtain biologic-free remission. Therefore, the identification of a novel therapeutic target for bone destructive diseases remains an important issue in the field of skeletal biology. To date there has been little progress in identifying osteo-innate-immunological regulators that could be used for the prophylactic treatment of inflammatory bone destruction. Recently, we identified several new molecules that are critical osteo-innate-immunological regulators by using gene targeting technology. These findings may offer an invaluable opportunity to regulate bone-destructive diseases, such as osteoporosis and rheumatoid arthritis. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:223 / 228
页数:6
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