C3G regulates cortical neuron migration, preplate splitting and radial glial cell attachment
Details
Publication Year 2008-06-15,Volume 135,Issue #12,Page 2139-2149
Journal Title
DEVELOPMENT
Publication Type
Journal Article
Abstract
Neuronal migration is integral to the development of the cerebral cortex and higher brain function. Cortical neuron migration defects lead to mental disorders such as lissencephaly and epilepsy. Interaction of neurons with their extracellular environment regulates cortical neuron migration through cell surface receptors. However, it is unclear how the signals from extracellular matrix proteins are transduced intracellularly. We report here that mouse embryos lacking the Ras family guanine nucleotide exchange factor, C3G (Rapgef1, Grf2), exhibit a cortical neuron migration defect resulting in a failure to split the preplate into marginal zone and subplate and a failure to form a cortical plate. C3G-deficient cortical neurons fail to migrate. Instead, they arrest in a multipolar state and accumulate below the preplate. The basement membrane is disrupted and radial glial processes are disorganised and lack attachment in C3G-deficient brains. C3G is activated in response to reelin in cortical neurons, which, in turn, leads to activation of the small GTPase Rap1. In C3G-deficient cells, Rap1 GTP loading in response to reelin stimulation is reduced. In conclusion, the Ras family regulator C3G is essential for two aspects of cortex development, namely radial glial attachment and neuronal migration.
Publisher
COMPANY OF BIOLOGISTS LTD
Keywords
EXCHANGE FACTOR C3G; DEVELOPING CEREBRAL-CORTEX; REELER-LIKE PHENOTYPE; CAJAL-RETZIUS CELLS; NEOCORTICAL DEVELOPMENT; EXTRACELLULAR-MATRIX; BASEMENT-MEMBRANE; BRAIN-DEVELOPMENT; MOUSE; RAP1
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2008-06-15 12:00:00
An error has occurred. This application may no longer respond until reloaded. Reload 🗙