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Direct Visualization of Actin Filaments and Actin-Binding Proteins in Neuronal Cells

机译:直接可视化肌动蛋白细丝和神经元细胞中的肌动蛋白结合蛋白

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Actin networks and actin-binding proteins (ABPs) are most abundant in the cytoskeleton of neurons. The function of ABPs in neurons is nucleation of actin polymerization, polymerization or depolymerization regulation, bundling of actin through crosslinking or stabilization, cargo movement along actin filaments, and anchoring of actin to other cellular components. In axons, ABP–actin interaction forms a dynamic, deep actin network, which regulates axon extension, guidance, axon branches, and synaptic structures. In dendrites, actin and ABPs are related to filopodia attenuation, spine formation, and synapse plasticity. ABP phosphorylation or mutation changes ABP–actin binding, which regulates axon or dendritic plasticity. In addition, hyperactive ABPs might also be expressed as aggregates of abnormal proteins in neurodegeneration. Those changes cause many neurological disorders. This review discusses ABPs related to neurological disorders. In addition, traditional or advanced electron microscopy (EM) techniques, such as negative-stained EM, cryo-EM, unroof using etching, freeze fracture, electron tomography, correlative light and electron microscopy, and 3D EM for direct visualization of ABP–actin interaction are reviewed using several examples.
机译:肌动蛋白网络和肌动蛋白结合蛋白(ABPS)在神经元的细胞骨架中最丰富。 ABPS在神经元中的功能是肌动蛋白聚合,聚合或解聚调节的成核,通过交联或稳定化,沿肌动蛋白细丝的货物运动和肌动蛋白锚固到其他细胞组分的锚定。在轴突中,ABP-Actin交互形成动态的深肌动蛋白网络,该网络调节轴突延伸,指导,轴突分支和突触结构。在树突中,肌动蛋白和ABP与缺氧衰减,脊柱形成和突触可塑性有关。 ABP磷酸化或突变变化ABP-actin结合,其调节轴突或树突塑性。此外,过度活跃的ABP也可以表达为神经变性异常蛋白质的聚集体。这些变化导致许多神经系统疾病。本次审查讨论了与神经系统疾病相关的ABPS。此外,传统或先进的电子显微镜(EM)技术(如负染色的EM,Cryo-EM,UnroOf)使用蚀刻,冷冻骨折,电子断层扫描,相关光和电子显微镜,以及用于直接可视化ABP-Actin的3D EM使用几个例子审查交互。

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