An adhesion signaling axis involving Dystroglycan, & beta;1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold

The mature mammalian cortex is composed of 6 architecturally and functionally distinct layers. Two key steps in the assembly of this layered structure are the initial establishment of the glial scaffold and the subsequent migration of postmitotic neurons to their final position. These processes involve the precise and timely regulation of adhesion and detachment of neural cells from their substrates. Although much is known about the roles of adhesive substrates during neuronal migration and the formation of the glial scaffold, less is understood about how these signals are interpreted and integrated within these neural cells. Here, we provide in vivo evidence that Cas proteins, a family of cytoplasmic adaptors, serve a functional and redundant role during cortical lamination. Cas triple conditional knock-out (Cas TcKO) mice display severe cortical phenotypes that feature cobblestone malformations. Molecular epistasis and genetic experiments suggest that Cas proteins act downstream of transmembrane Dystroglycan and & beta;1-Integrin in a radial glial cell-autonomous manner. Overall, these data establish a new and essential role for Cas adaptor proteins during the formation of cortical circuits and reveal a signaling axis controlling cortical scaffold formation.

Automated summary

The mature mammalian cortex is composed of 6 architecturally and functionally distinct layers. The assembly of this layered structure involves the establishment of the glial scaffold and the migration of postmitotic neurons. Cas proteins play a functional and redundant role during cortical lamination, acting downstream of transmembrane Dystroglycan and β1-Integrin in a radial glial cell-autonomous manner. These findings establish a new and essential role for Cas adaptor proteins in cortical circuit formation and scaffold formation.