中心体
微管
微管形核
轴突
生物
细胞生物学
电池极性
微管蛋白
神经科学
轴突引导
细胞
细胞周期
遗传学
作者
Stanislav Vinopal,Sebastián Dupraz,Eissa Alfadil,Thorben Pietralla,Shweta Bendre,Michael Stieß,Sven Falk,Germán Camargo Ortega,Nicola Maghelli,Iva M. Tolić,Jiří Smejkal,Magdalena Götz,Frank Bradke
出处
期刊:Neuron
[Elsevier]
日期:2023-04-01
卷期号:111 (8): 1241-1263.e16
被引量:7
标识
DOI:10.1016/j.neuron.2023.01.020
摘要
Cortical projection neurons polarize and form an axon while migrating radially. Even though these dynamic processes are closely interwoven, they are regulated separately-the neurons terminate their migration when reaching their destination, the cortical plate, but continue to grow their axons. Here, we show that in rodents, the centrosome distinguishes these processes. Newly developed molecular tools modulating centrosomal microtubule nucleation combined with in vivo imaging uncovered that dysregulation of centrosomal microtubule nucleation abrogated radial migration without affecting axon formation. Tightly regulated centrosomal microtubule nucleation was required for periodic formation of the cytoplasmic dilation at the leading process, which is essential for radial migration. The microtubule nucleating factor γ-tubulin decreased at neuronal centrosomes during the migratory phase. As distinct microtubule networks drive neuronal polarization and radial migration, this provides insight into how neuronal migratory defects occur without largely affecting axonal tracts in human developmental cortical dysgeneses, caused by mutations in γ-tubulin.
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