Literature DB >> 31400545

Regulation of osteoclast function via Rho-Pkn3-c-Src pathways.

Shunsuke Uehara1, Nobuyuki Udagawa2, Yasuhiro Kobayashi3.   

Abstract

BACKGROUND: Wnt signaling pathways are largely divided into the β-catenin-dependent canonical pathway and β-catenin-independent non-canonical pathways. The roles of Wnt signaling in bone metabolism have been extensively investigated. We previously attempted to clarify the roles of Wnt-non-canonical signaling in bone resorption and demonstrated that Wnt5a-receptor tyrosine kinase-like orphan receptor 2 (Ror2) signaling promoted osteoclast differentiation by enhancing RANK expression in osteoclast precursor cells. However, the roles of Wnt5a-Ror2 signaling in osteoclast function remain unclear. HIGHLIGHT: Trabecular bone mass was significantly greater in osteoclast-specific Ror2-deficient (Ror2ΔOCL/ΔOCL) mice than in control mice due to the decreased bone-resorbing activity of osteoclasts. Wnt5a-Ror2 signaling activated Rho in osteoclasts via dishevelled-associated activator of morphogenesis 2 (Daam2). The expression of protein kinase N3 (Pkn3), a Rho effector, increased during osteoclast differentiation. Trabecular bone mass was significantly greater in Pkn3-deficient mice than in wild-type mice due to the decreased bone-resorbing activity of osteoclasts. Pkn3 bound to c-Src and Pyk2 in a Wnt5a-Ror2 signaling-dependent manner, thereby enhancing the kinase activity of c-Src in osteoclasts. The binding of Pkn3 to c-Src was essential for the bone-resorbing activity of osteoclasts.
CONCLUSION: Wnt5a-Ror2 signaling promotes the bone-resorbing activity of osteoclasts by activating the Daam2-Rho-Pkn3-c-Src pathways. Pkn3 inhibitors, therefore, have potential as therapeutic agents for osteoporosis and bone destruction in inflammatory diseases.
Copyright © 2019 Japanese Association for Oral Biology. All rights reserved.

Entities:  

Keywords:  Actin cytoskeleton; Bone resorption; Osteoclast; Protein-serine-threonine kinases; Wnt5a protein

Mesh:

Substances:

Year:  2019        PMID: 31400545     DOI: 10.1016/j.job.2019.07.002

Source DB:  PubMed          Journal:  J Oral Biosci        ISSN: 1349-0079


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