| Literature DB >> 27681594 |
Kenta Maruyama1, Takahiko Kawasaki2, Masahide Hamaguchi3, Motomu Hashimoto4, Moritoshi Furu4, Hiromu Ito4, Takao Fujii4, Naoki Takemura5, Thangaraj Karuppuchamy6, Takeshi Kondo6, Takumi Kawasaki6, Masahiro Fukasaka6, Takuma Misawa6, Tatsuya Saitoh6,7, Yutaka Suzuki8, Mikaël M Martino6,9, Yutaro Kumagai6, Shizuo Akira10,11.
Abstract
Netrin 1 was initially identified as an axon guidance factor, and recent studies indicate that it inhibits chemokine-directed monocyte migration. Despite its importance as a neuroimmune guidance cue, the role of netrin 1 in osteoclasts is largely unknown. Here we detected high netrin 1 levels in the synovial fluid of rheumatoid arthritis patients. Netrin 1 is potently expressed in osteoblasts and synovial fibroblasts, and IL-17 robustly enhances netrin 1 expression in these cells. The binding of netrin 1 to its receptor UNC5b on osteoclasts resulted in activation of SHP1, which inhibited VAV3 phosphorylation and RAC1 activation. This significantly impaired the actin polymerization and fusion, but not the differentiation of osteoclast. Strikingly, netrin 1 treatment prevented bone erosion in an autoimmune arthritis model and age-related bone destruction. Therefore, the netrin 1-UNC5b axis is a novel therapeutic target for bone-destructive diseases.Entities:
Keywords: arthritis; cell fusion; interleukin 17A (IL-17 or IL-17A); netrin 1; osteoblast; osteoclast; osteoporosis; rheumatoid arthritis
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Year: 2016 PMID: 27681594 PMCID: PMC5104911 DOI: 10.1074/jbc.M116.738518
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157