| Literature DB >> 26511243 |
Chundi Xu1, Yasuhiro Funahashi1, Takashi Watanabe1, Tetsuya Takano1, Shinichi Nakamuta1, Takashi Namba1, Kozo Kaibuchi2.
Abstract
How extracellular cues direct axon-dendrite polarization in mouse developing neurons is not fully understood. Here, we report that the radial glial cell (RGC)-cortical neuron interaction directs axon formation at the opposite side of the neuron from the contact site. N-cadherin accumulates at the contact site between the RGC and cortical neuron. Inhibition of the N-cadherin-mediated adhesion decreases this oriented axon formation in vitro, and disrupts the axon-dendrite polarization in vivo. Furthermore, the RGC-neuron interaction induces the polarized distribution of active RhoA at the contacting neurite and active Rac1 at the opposite neurite. Inhibition of Rho-Rho-kinase signaling in a neuron impairs the oriented axon formation in vitro, and prevents axon-dendrite polarization in vivo. Collectively, these results suggest that the N-cadherin-mediated radial glia-neuron interaction determines the contacting neurite as the leading process for radial glia-guided neuronal migration and directs axon formation to the opposite side acting through the Rho family GTPases.Entities:
Keywords: N-cadherin; RhoA; axon formation; axon–dendrite polarization; cell–cell interaction; radial glial cell
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Year: 2015 PMID: 26511243 PMCID: PMC4623227 DOI: 10.1523/JNEUROSCI.1266-15.2015
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167