Department of Cell and Developmental Biology, University College London, London WC1E 6BT, United Kingdom.
J Neurosci. 2013 Feb 6;33(6):2661-70. doi: 10.1523/JNEUROSCI.0998-12.2013.
Neuronal activity regulates the formation and morphology of dendritic spines through changes in the actin cytoskeleton. However, the molecular mechanisms that regulate this process remain poorly understood. Here we report that Eps8, an actin-capping protein, is required for spine morphogenesis. In rat hippocampal neurons, gain- and loss-of-function studies demonstrate that Eps8 promotes the formation of dendritic spines but inhibits filopodium formation. Loss of function of Eps8 increases actin polymerization and induces fast actin turnover within dendritic spines, as revealed by free-barbed end and FRAP assays, consistent with a role for Eps8 as an actin-capping protein. Interestingly, Eps8 regulates the balance between excitatory synapses on spines and on the dendritic shaft, without affecting the total number of synapses or basal synaptic transmission. Importantly, Eps8 loss of function impairs the structural and functional plasticity of synapses induced by long-term potentiation. These findings demonstrate a novel role for Eps8 in spine formation and in activity-mediated synaptic plasticity.
神经元活动通过改变肌动蛋白细胞骨架来调节树突棘的形成和形态。然而,调节这个过程的分子机制仍知之甚少。在这里,我们报告说 Eps8,一种肌动蛋白加帽蛋白,是树突棘形态发生所必需的。在大鼠海马神经元中,功能获得和功能丧失研究表明 Eps8 促进树突棘的形成,但抑制丝状伪足的形成。Eps8 的功能丧失会增加肌动蛋白聚合,并诱导树突棘内快速肌动蛋白周转,这可以通过游离端和 FRAP 测定来揭示,与 Eps8 作为肌动蛋白加帽蛋白的作用一致。有趣的是,Eps8 调节棘突和树突干上兴奋性突触之间的平衡,而不影响突触的总数或基础突触传递。重要的是,Eps8 的功能丧失会损害由长时程增强诱导的突触的结构和功能可塑性。这些发现表明 Eps8 在棘突形成和活动介导的突触可塑性中具有新的作用。