Freeman Sean A, Desmazières Anne, Simonnet Jean, Gatta Marie, Pfeiffer Friederike, Aigrot Marie Stéphane, Rappeneau Quentin, Guerreiro Serge, Michel Patrick Pierre, Yanagawa Yuchio, Barbin Gilles, Brophy Peter J, Fricker Desdemona, Lubetzki Catherine, Sol-Foulon Nathalie
Sorbonne Universités Université Pierre et Marie Curie University of Paris 06, UMR_S 1127, Institut du Cerveau et de la Moelle-Groupe Hospitalo-Universitaire Pitié-Salpêtrière, F-75013, Paris, France; INSERM U1127, F-75013, Paris, France; CNRS UMR7225, F-75013, Paris, France;
Department of Genetic and Behavioral Neuroscience, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan; Japan Science and Technology Agency, Tokyo 102-8666, Japan;
Proc Natl Acad Sci U S A. 2015 Jan 20;112(3):E321-8. doi: 10.1073/pnas.1419099112. Epub 2015 Jan 5.
High-density accumulation of voltage-gated sodium (Nav) channels at nodes of Ranvier ensures rapid saltatory conduction along myelinated axons. To gain insight into mechanisms of node assembly in the CNS, we focused on early steps of nodal protein clustering. We show in hippocampal cultures that prenodes (i.e., clusters of Nav channels colocalizing with the scaffold protein ankyrinG and nodal cell adhesion molecules) are detected before myelin deposition along axons. These clusters can be induced on purified neurons by addition of oligodendroglial-secreted factor(s), whereas ankyrinG silencing prevents their formation. The Nav isoforms Nav1.1, Nav1.2, and Nav1.6 are detected at prenodes, with Nav1.6 progressively replacing Nav1.2 over time in hippocampal neurons cultured with oligodendrocytes and astrocytes. However, the oligodendrocyte-secreted factor(s) can induce the clustering of Nav1.1 and Nav1.2 but not of Nav1.6 on purified neurons. We observed that prenodes are restricted to GABAergic neurons, whereas clustering of nodal proteins only occurs concomitantly with myelin ensheathment on pyramidal neurons, implying separate mechanisms of assembly among different neuronal subpopulations. To address the functional significance of these early clusters, we used single-axon electrophysiological recordings in vitro and showed that prenode formation is sufficient to accelerate the speed of axonal conduction before myelination. Finally, we provide evidence that prenodal clusters are also detected in vivo before myelination, further strengthening their physiological relevance.
电压门控钠(Nav)通道在郎飞结处的高密度聚集确保了沿有髓轴突的快速跳跃式传导。为深入了解中枢神经系统中节点组装的机制,我们聚焦于节点蛋白聚集的早期步骤。我们在海马培养物中发现,在轴突上髓鞘沉积之前就能检测到前节点(即与支架蛋白锚蛋白G和节点细胞粘附分子共定位的Nav通道簇)。通过添加少突胶质细胞分泌的因子,这些簇可以在纯化的神经元上诱导形成,而沉默锚蛋白G则会阻止它们的形成。在前节点处检测到Nav亚型Nav1.1、Nav1.2和Nav1.6,在与少突胶质细胞和星形胶质细胞一起培养的海马神经元中,随着时间的推移,Nav1.6逐渐取代Nav1.2。然而,少突胶质细胞分泌的因子可以在纯化的神经元上诱导Nav1.1和Nav1.2的聚集,但不能诱导Nav1.6的聚集。我们观察到前节点仅限于GABA能神经元,而节点蛋白的聚集仅在锥体细胞的髓鞘包裹时才会发生,这意味着不同神经元亚群之间存在不同的组装机制。为了探究这些早期簇的功能意义,我们在体外使用单轴突电生理记录,结果表明前节点的形成足以在髓鞘形成之前加速轴突传导速度。最后,我们提供证据表明在体内髓鞘形成之前也能检测到前节点簇,进一步加强了它们的生理相关性。