Neuroscience Graduate Group, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Traffic. 2017 Dec;18(12):808-824. doi: 10.1111/tra.12529.
The unique polarization of neurons depends on selective sorting of axonal and somatodendritic cargos to their correct compartments. Axodendritic sorting and filtering occurs within the axon initial segment (AIS). However, the underlying molecular mechanisms responsible for this filter are not well understood. Here, we show that local activation of the neuronal-specific kinase cyclin-dependent kinase 5 (CDK5) is required to maintain AIS integrity, as depletion or inhibition of CDK5 induces disordered microtubule polarity and loss of AIS cytoskeletal structure. Furthermore, CDK5-dependent phosphorylation of the dynein regulator Ndel1 is required for proper re-routing of mislocalized somatodendritic cargo out of the AIS; inhibition of this pathway induces profound mis-sorting defects. While inhibition of the CDK5-Ndel1-Lis1-dynein pathway alters both axonal microtubule polarity and axodendritic sorting, we found that these defects occur on distinct timescales; brief inhibition of dynein disrupts axonal cargo sorting before loss of microtubule polarity becomes evident. Together, these studies identify CDK5 as a master upstream regulator of trafficking in vertebrate neurons, required for both AIS microtubule organization and polarized dynein-dependent sorting of axodendritic cargos, and support an ongoing and essential role for dynein at the AIS.
神经元的独特极化依赖于轴突和树突质货物到其正确隔室的选择性分拣。轴突树突分拣和过滤发生在轴突起始段 (AIS) 内。然而,负责这种筛选的潜在分子机制尚不清楚。在这里,我们表明,神经元特异性激酶细胞周期蛋白依赖性激酶 5 (CDK5) 的局部激活对于维持 AIS 的完整性是必需的,因为 CDK5 的耗竭或抑制会诱导微管极性紊乱和 AIS 细胞骨架结构的丧失。此外,CDK5 依赖性磷酸化动力蛋白调节剂 Ndel1 对于正确重路由错误定位的树突质货物出 AIS 是必需的; 抑制这条途径会引起严重的分拣缺陷。虽然抑制 CDK5-Ndel1-Lis1-动力蛋白途径会改变轴突微管极性和轴突树突分拣,但我们发现这些缺陷发生在不同的时间尺度上; 短暂抑制动力蛋白会在微管极性丧失变得明显之前破坏轴突货物分拣。总之,这些研究确定 CDK5 是脊椎动物神经元中运输的主要上游调节剂,对于 AIS 微管组织和极化动力蛋白依赖性轴突树突货物分拣都是必需的,并支持动力蛋白在 AIS 中的持续和基本作用。