Department of Molecular, Cellular and Developmental Neurobiology, Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
PLoS One. 2010 Sep 23;5(9):e12908. doi: 10.1371/journal.pone.0012908.
The development of morphological neuronal polarity starts by the formation and elongation of an axon. At the same time the axon initial segment (AIS) is generated and creates a diffusion barrier which differentiate axon and somatodendritic compartment. Different structural and functional proteins that contribute to the generation of neuronal action potential are concentrated at the axon initial segment. While axonal elongation is controlled by signalling pathways that regulate cytoskeleton through microtubule associated proteins and tubulin modifications, the microtubule cytoskeleton under the AIS is mostly unknown. Thus, understanding which proteins modify tubulin, where in the neuron and at which developmental stage is crucial to understanding how morphological and functional neuronal polarity is achieved. In this study performed in mice and using a well established model of murine cultured hippocampal neurons, we report that the tubulin deacetylase HDAC6 is localized at the distal region of the axon, and its inhibition with TSA or tubacin slows down axonal growth. Suppression of HDAC6 expression with HDAC6 shRNAs or expression of a non-active mutant of HDAC6 also reduces axonal length. Furthermore, HDAC6 inhibition or suppression avoids the concentration of ankyrinG and sodium channels at the axon initial segment (AIS). Moreover, treatment of mouse cultured hippocampal neurons with detergents to eliminate the soluble pool of microtubules identified a pool of detergent resistant acetylated microtubules at the AIS, not present at the rest of the axon. Inhibition or suppression of HDAC6 increases acetylation all along the axon and disrupts the specificity of AIS cytoskeleton, modifying the axonal distal gradient localization of KIF5C to a somatodendritic and axonal localization. In conclusion, our results reveal a new role of HDAC6 tubulin deacetylase as a regulator of microtubule characteristics in the axon distal region where axonal elongation takes place, and allowing the development of acetylated microtubules microdomains where HDAC6 is not concentrated, such as the axon initial segment.
神经元形态极性的发展始于轴突的形成和伸长。与此同时,轴突起始段(AIS)生成并产生扩散屏障,将轴突和体树突隔室区分开来。有助于产生神经元动作电位的不同结构和功能蛋白集中在轴突起始段。虽然轴突伸长受信号通路的控制,这些信号通路通过微管相关蛋白和微管蛋白修饰来调节细胞骨架,但 AIS 下的微管细胞骨架知之甚少。因此,了解哪些蛋白质修饰微管蛋白,在神经元中的哪个位置以及在哪个发育阶段对于理解如何实现形态和功能神经元极性至关重要。在这项在小鼠中进行的研究中,我们使用了一种成熟的小鼠培养海马神经元模型,报告说微管去乙酰化酶 HDAC6 定位于轴突的远端区域,其抑制作用 TSA 或 tubacin 会减缓轴突生长。用 HDAC6 shRNAs 抑制 HDAC6 表达或表达非活性突变型 HDAC6 也会减少轴突长度。此外,HDAC6 抑制或抑制作用可避免 ankyrinG 和钠通道在轴突起始段(AIS)的集中。此外,用去污剂处理培养的海马神经元以消除微管的可溶性池,在 AIS 处鉴定出存在于其余轴突处不存在的去污剂抗性乙酰化微管池。HDAC6 的抑制或抑制作用增加了整个轴突的乙酰化,并破坏了 AIS 细胞骨架的特异性,将 KIF5C 的轴突远端梯度定位改变为体树突和轴突定位。总之,我们的结果揭示了 HDAC6 微管去乙酰化酶作为发生轴突伸长的轴突远端区域微管特征调节剂的新作用,并允许形成乙酰化微管微区,其中 HDAC6 没有集中,例如轴突起始段。