| Literature DB >> 24559674 |
Takashi Namba1, Yuji Kibe1, Yasuhiro Funahashi1, Shinichi Nakamuta1, Tetsuya Takano1, Takuji Ueno1, Akiko Shimada1, Sachi Kozawa1, Mayumi Okamoto2, Yasushi Shimoda3, Kanako Oda4, Yoshino Wada5, Tomoyuki Masuda6, Akira Sakakibara2, Michihiro Igarashi5, Takaki Miyata2, Catherine Faivre-Sarrailh7, Kosei Takeuchi8, Kozo Kaibuchi9.
Abstract
The polarization of neurons, which mainly includes the differentiation of axons and dendrites, is regulated by cell-autonomous and non-cell-autonomous factors. In the developing central nervous system, neuronal development occurs in a heterogeneous environment that also comprises extracellular matrices, radial glial cells, and neurons. Although many cell-autonomous factors that affect neuronal polarization have been identified, the microenvironmental cues involved in neuronal polarization remain largely unknown. Here, we show that neuronal polarization occurs in a microenvironment in the lower intermediate zone, where the cell adhesion molecule transient axonal glycoprotein-1 (TAG-1) is expressed in cortical efferent axons. The immature neurites of multipolar cells closely contact TAG-1-positive axons and generate axons. Inhibition of TAG-1-mediated cell-to-cell interaction or its downstream kinase Lyn impairs neuronal polarization. These results show that the TAG-1-mediated cell-to-cell interaction between the unpolarized multipolar cells and the pioneering axons regulates the polarization of multipolar cells partly through Lyn kinase and Rac1.Entities:
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Year: 2014 PMID: 24559674 DOI: 10.1016/j.neuron.2013.12.015
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173