Autor: |
Wong, Wenny, Estep, Jason A., Treptow, Alyssa M., Rajabli, Niloofar, Jahncke, Jennifer N., Ubina, Teresa, Wright, Kevin M., Riccomagno, Martin M. |
Předmět: |
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Zdroj: |
PLoS Biology; 8/4/2023, Vol. 21 Issue 8, p1-43, 43p, 2 Color Photographs, 1 Chart, 12 Graphs |
Abstrakt: |
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 β1-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. The assembly of a radial glial scaffold is a key step during cortical migration; this study demonstrates that Cas adaptor proteins act downstream of Dystroglycan and b1-Integrin during the establishment of this glial scaffold to regulate cortical lamination. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
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