Journal of Biological Chemistry 291(46): 23854-23868
Article 2016 English
Authors
KM
Kenta Maruyama
TK
Takahiko Kawasaki
MH
Masahide Hamaguchi
Abstract
1 min read
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.
Bruno Larrivée, Catarina Freitas, Marc Trombe, Xiang Lv, Benjamin DeLafarge, Yuan Li, Karine Bouvrée, Christiane Bréant, R. Toro, Nicolas Bréchot, Stéphane Germain, Françoise Bono, Frédérique Dol, Filip Claes, Christian Fischer, Monica Autiero, Jean‐Léon Thomas, Peter Carmeliet, Marc Tessier‐Lavigne, Anne Eichmann
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