コンテンツへスキップ
Merck

Cell-Intrinsic Control of Interneuron Migration Drives Cortical Morphogenesis.

Cell (2018-02-24)
Carla G Silva, Elise Peyre, Mohit H Adhikari, Sylvia Tielens, Sebastian Tanco, Petra Van Damme, Lorenza Magno, Nathalie Krusy, Gulistan Agirman, Maria M Magiera, Nicoletta Kessaris, Brigitte Malgrange, Annie Andrieux, Carsten Janke, Laurent Nguyen
要旨

Interneurons navigate along multiple tangential paths to settle into appropriate cortical layers. They undergo a saltatory migration paced by intermittent nuclear jumps whose regulation relies on interplay between extracellular cues and genetic-encoded information. It remains unclear how cycles of pause and movement are coordinated at the molecular level. Post-translational modification of proteins contributes to cell migration regulation. The present study uncovers that carboxypeptidase 1, which promotes post-translational protein deglutamylation, controls the pausing of migrating cortical interneurons. Moreover, we demonstrate that pausing during migration attenuates movement simultaneity at the population level, thereby controlling the flow of interneurons invading the cortex. Interfering with the regulation of pausing not only affects the size of the cortical interneuron cohort but also impairs the generation of age-matched projection neurons of the upper layers.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
抗βアクチン−ペルオキシダーゼ抗体、マウスモノクローナル マウス宿主抗体, clone AC-15, purified from hybridoma cell culture
Sigma-Aldrich
モノクロナール抗チューブリン, アセチル化 マウス宿主抗体, clone 6-11B-1, ascites fluid
Sigma-Aldrich
抗マウスIgG (Fc特異的) ヤギ宿主抗体, 2.0 mg/mL, affinity isolated antibody
Sigma-Aldrich
抗チューブリン抗体、δ 2, Chemicon®, from rabbit
Sigma-Aldrich
モノクロナール抗ミオシン軽鎖キナーゼ マウス宿主抗体, clone K36, ascites fluid
Sigma-Aldrich
Anti-CUX1 Antibody, a.a. 861, from rabbit, purified by affinity chromatography