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Article

Ror2/Frizzled Complex Mediates Wnt5a-Induced AP-1 Activation by Regulating Dishevelled Polymerization

, , , , , , , , & show all
Pages 3610-3619 | Received 12 Feb 2010, Accepted 27 Apr 2010, Published online: 20 Mar 2023
 

Abstract

The receptor tyrosine kinase Ror2 acts as a receptor or coreceptor for Wnt5a to mediate Wnt5a-induced activation of the Wnt/JNK pathway and inhibition of the β-catenin-dependent canonical Wnt pathway. However, little is known about how Ror2 cooperates with another receptor component(s) to mediate Wnt5a signaling. We show here that Ror2 regulates Wnt5a-induced polymerization of Dishevelled (Dvl) and that this Ror2-mediated regulation of Dvl is independent of the cytoplasmic region of Ror2. Ror2 can associate with Frizzled7 (Fz7) via its extracellular cysteine-rich domain to form a receptor complex that is required for the regulation of Dvl and activation of the AP-1 promoter after Wnt5a stimulation. Suppressed expression of Fz7 indeed results in the inhibition of Wnt5a-induced polymerization of Dvl and AP-1 activation. Interestingly, both the DIX and the DEP domains of Dvl are indispensable for Dvl polymerization and subsequent AP-1 activation after Wnt5a stimulation. We further show that polymerized Dvl is colocalized with Rac1 and that suppressed expression of Rac1 inhibits Wnt5a-induced AP-1 activation. Collectively, our results indicate that Ror2/Fz receptor complex plays an important role in the Wnt5a/Rac1/AP-1 pathway by regulating the polymerization of Dvl.

Supplemental material for this article may be found at http://mcb.asm.org/.

We thank Randall T. Moon (University of Washington School of Medicine, Seattle) for the SuperTopFlash.

This study was supported by Grants-in-Aid for Scientific Research, for Scientific Research on Priority Areas, for Scientific Research (B), for Young Scientists, and for the Global Center of Excellence Program from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and by a grant from the Takeda Science Foundation.

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