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Publication : TrkB regulates neocortex formation through the Shc/PLCgamma-mediated control of neuronal migration.

First Author  Medina DL Year  2004
Journal  EMBO J Volume  23
Issue  19 Pages  3803-14
PubMed ID  15372074 Mgi Jnum  J:132562
Mgi Id  MGI:3776308 Doi  10.1038/sj.emboj.7600399
Citation  Medina DL, et al. (2004) TrkB regulates neocortex formation through the Shc/PLCgamma-mediated control of neuronal migration. EMBO J 23(19):3803-14
abstractText  The generation of complex neuronal structures, such as the neocortex, requires accurate positioning of neurons and glia within the structure, followed by differentiation, formation of neuronal connections, and myelination. To understand the importance of TrkB signaling during these events, we have used conditional and knockin mutagenesis of the TrkB neurotrophin receptor, and we now show that this tyrosine kinase receptor, through docking sites for the Shc/FRS2 adaptors and phospholipase Cgamma (PLCgamma), coordinates these events in the cerebral cortex by (1) controlling cortical stratification through the timing of neuronal migration during cortex formation, and (2) regulating both neuronal and oligodendrocyte differentiation. These results provide genetic evidence that TrkB regulates important functions throughout the formation of the cerebral cortex via recruitment of the Shc/FRS2 adaptors and PLCgamma.
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