ID | 119230 |
Title Alternative | Role of Netrin 1 in Bone Homeostasis
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Author |
Maruyama, Kenta
Osaka University
Kawasaki, Takahiko
National Institute of Genetics
Hamaguchi, Masahide
Osaka University
Hashimoto, Motomu
Kyoto University
Furu, Moritoshi
Kyoto University
Ito, Hiromu
Kyoto University
Fujii, Takao
Kyoto University
Takemura, Naoki
The University of Tokyo
Karuppuchamy, Thangaraj
Osaka University
Kondo, Takeshi
Osaka University
Kawasaki, Takumi
Osaka University
Fukasaka, Masahiro
Osaka University
Misawa, Takuma
Osaka University
Suzuki, Yutaka
The University of Tokyo
Martino, Mikaël M.
Osaka University|Monash University
Kumagai, Yutaro
Osaka University
Akira, Shizuo
Osaka University
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Content Type |
Journal Article
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Description | 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.
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Journal Title |
Journal of Biological Chemistry
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ISSN | 00219258
1083351X
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NCID | AA1202441X
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Publisher | American Society for Biochemistry and Molecular Biology|Elsevier
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Volume | 291
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Issue | 46
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Start Page | 23854
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End Page | 23868
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Published Date | 2016-09-28
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Rights | This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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DOI (Published Version) | |
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language |
eng
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Publisher
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departments |
Institute of Advanced Medical Sciences
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