Reelin Regulates Cadherin Function via Dab1/Rap1 to Control Neuronal Migration and Lamination in the Neocortex

• Published in: Neuron (Cambridge, Mass.) Mass.), 2011-02, Vol.69 (3), p.482-497
• Main Authors: Franco, Santos J., Martinez-Garay, Isabel, Gil-Sanz, Cristina, Harkins-Perry, Sarah R., Müller, Ulrich
• Format: Article
• Language: English
• Subjects: Animals; Basement Membrane - physiology; Cadherins - genetics; Cadherins - physiology; Cell Adhesion Molecules, Neuronal - genetics; Cell Adhesion Molecules, Neuronal - physiology; Cell Movement - genetics; Cell Movement - physiology; Defects; Experiments; Extracellular Matrix Proteins - genetics; Extracellular Matrix Proteins - physiology; Female; Gene Knock-In Techniques; Kinases; Mice; Mice, Knockout; Mice, Neurologic Mutants; Mice, Transgenic; Microscopy; Neocortex - embryology; Neocortex - physiology; Nerve Tissue Proteins - genetics; Nerve Tissue Proteins - physiology; Neurons; Neurons - physiology; rap1 GTP-Binding Proteins - genetics; rap1 GTP-Binding Proteins - physiology; Serine Endopeptidases - genetics; Serine Endopeptidases - physiology
• ISSN: 0896-6273; 1097-4199
• DOI: 10.1016/j.neuron.2011.01.003

Neuronal migration is critical for establishing neocortical cell layers and migration defects can cause neurological and psychiatric diseases. Recent studies show that radially migrating neocortical neurons use glia-dependent and glia-independent modes of migration, but the signaling pathways that control different migration modes and the transitions between them are poorly defined. Here, we show that Dab1, an essential component of the reelin pathway, is required in radially migrating neurons for glia-independent somal translocation, but not for glia-guided locomotion. During migration, Dab1 acts in translocating neurons to stabilize their leading processes in a Rap1-dependent manner. Rap1, in turn, controls cadherin function to regulate somal translocation. Furthermore, cell-autonomous neuronal deficits in somal translocation are sufficient to cause severe neocortical lamination defects. Thus, we define the cellular mechanism of reelin function during radial migration, elucidate the molecular pathway downstream of Dab1 during somal translocation, and establish the importance of glia-independent motility in neocortical development. ► Dab1 is necessary for glia-independent translocation, but not other migration modes ► The Dab1 effector Rap1 controls cadherin function during glia-independent migration ► Neuron-specific knockout of Dab1 phenocopies reeler lamination defects ► Preplate splitting is not sufficient to permit layering of later-born Dab1 null cells