| Literature DB >> 26893343 |
Xuejun Chai1, Shanting Zhao2, Li Fan3, Wei Zhang4, Xi Lu4, Hong Shao3, Shaobo Wang1, Lingzhen Song1, Antonio Virgilio Failla5, Bernd Zobiak5, Hans G Mannherz6, Michael Frotscher7.
Abstract
In reeler mutant mice, which are deficient in reelin (Reln), the lamination of the cerebral cortex is disrupted. Reelin signaling induces phosphorylation of LIM kinase 1, which phosphorylates the actin-depolymerizing protein cofilin in migrating neurons. Conditional cofilin mutants show neuronal migration defects. Thus, both reelin and cofilin are indispensable during cortical development. To analyze the effects of cofilin phosphorylation on neuronal migration we used in utero electroporation to transfect E14.5 wild-type cortical neurons with pCAG-EGFP plasmids encoding either a nonphosphorylatable form of cofilin 1 (cofilin(S3A)), a pseudophosphorylated form (cofilin(S3E)) or wild-type cofilin 1 (cofilin(WT)). Wild-type controls and reeler neurons were transfected with pCAG-EGFP. Real-time microscopy and histological analyses revealed that overexpression of cofilin(WT) and both phosphomutants induced migration defects and morphological abnormalities of cortical neurons. Of note, reeler neurons and cofilin(S3A)- and cofilin(S3E)-transfected neurons showed aberrant backward migration towards the ventricular zone. Overexpression of cofilin(S3E), the pseudophosphorylated form, partially rescued the migration defect of reeler neurons, as did overexpression of Limk1. Collectively, the results indicate that reelin and cofilin cooperate in controlling cytoskeletal dynamics during neuronal migration.Entities:
Keywords: Actin cytoskeleton; Cofilin phosphorylation; In utero electroporation; Neuronal migration; Reelin signaling
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Year: 2016 PMID: 26893343 DOI: 10.1242/dev.134163
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868