Scientific article
English

The serotonin 6 receptor controls neuronal migration during corticogenesis via a ligand-independent Cdk5-dependent mechanism

Published inDevelopment, vol. 141, no. 17, p. 3370-3377
Publication date2014
Abstract

The formation of a laminar structure such as the mammalian neocortex relies on the coordinated migration of different subtypes of excitatory pyramidal neurons in specific layers. Cyclin-dependent kinase 5 (Cdk5) is a master regulator of pyramidal neuron migration. Recently, we have shown that Cdk5 binds to the serotonin 6 receptor (5-HT6R), a G protein-coupled receptor (GPCR). Here, we investigated the role of 5-HT6R in the positioning and migration of pyramidal neurons during mouse corticogenesis. We report that constitutive expression of 5-HT6R controls pyramidal neuron migration through an agonist-independent mechanism that requires Cdk5 activity. These data provide the first in vivo evidence of a role for constitutive activity at a GPCR in neocortical radial migration.

Keywords
  • Animals
  • Cell Movement
  • Cerebral Cortex/cytology/metabolism
  • Cyclin-Dependent Kinase 5/metabolism
  • Down-Regulation
  • Female
  • HEK293 Cells
  • Humans
  • Ligands
  • Mice
  • Mice, Inbred C57BL
  • Neurogenesis
  • Neurons/cytology/metabolism
  • Pyramidal Cells/cytology/metabolism
  • Receptors, Serotonin/genetics/metabolism
  • Substrate Specificity
Citation (ISO format)
JACOBSHAGEN, Moritz et al. The serotonin 6 receptor controls neuronal migration during corticogenesis via a ligand-independent Cdk5-dependent mechanism. In: Development, 2014, vol. 141, n° 17, p. 3370–3377. doi: 10.1242/dev.108043
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Article (Published version)
accessLevelRestricted
Identifiers
Journal ISSN0950-1991
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