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首页> 外文期刊>Molecular brain >Stimulation-induced differential redistributions of clathrin and clathrin-coated vesicles in axons compared to soma/dendrites
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Stimulation-induced differential redistributions of clathrin and clathrin-coated vesicles in axons compared to soma/dendrites

机译:与SOMA / DENDRITES相比,刺激诱导的轴突和克拉氏蛋白涂层囊泡的差异再分布

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Clathrin-mediated endocytosis plays an important role in the recycling of synaptic vesicle in presynaptic terminals, and in the recycling of transmitter receptors in neuronal soma/dendrites. The present study uses electron microscopy (EM) and immunogold EM to document the different categories of clathrin-coated vesicles (CCV) and pits (CCP) in axons compared to soma/dendrites, and the depolarization-induced redistribution of clathrin in these two polarized compartments of the neuron. The size of CCVs in presynaptic terminals (~?40?nm; similar to the size of synaptic vesicles) is considerably smaller than the size of CCVs in soma/dendrites (~?90?nm). Furthermore, neuronal stimulation induces an increase in the number of CCV/CCP in presynaptic terminals, but a decrease in soma/dendrites. Immunogold labeling of clathrin revealed that in presynaptic terminals under resting conditions, the majority of clathrin molecules are unassembled and concentrated outside of synaptic vesicle clusters. Upon depolarization with high K , label for clathrin became scattered among de-clustered synaptic vesicles and moved closer to the presynaptic active zone. In contrast to axons, clathrin-labeled CCVs and CCPs were prominent in soma/dendrites under resting conditions, and became inconspicuous upon depolarization with high K . Thus, EM examination suggests that the regulation and mechanism of clathrin-mediated endocytosis differ between axon and dendrite, and that clathrin redistributes differently in these two neuronal compartments upon depolarization.
机译:Clathrin介导的内吞作用在突触前末端的突触囊泡的再循环中起着重要作用,以及神经元躯体/树突中的发射器受体的再循环。与Soma / dendrites相比,本研究使用电子显微镜(EM)和免疫射频EM在轴突中记录轴突中的不同类别的克拉辛涂覆的囊泡(CCV)和凹坑(CCP),以及在这两种极化中的克拉仑的去极化诱导的再分布神经元的隔间。在突触前终端中CCV的大小(〜40?NM;类似于突触囊泡的尺寸)比SOMA /树枝状物(〜90≤nm)中的CCV的大小相当小。此外,神经元刺激诱导突触前末端中CCV / CCP的数量增加,但SOMA / DENDRITES的降低。克拉汀的免疫形状标记显示,在静止条件下的突触前末端,大多数克拉仑分子都是未组装的,并浓缩在突触囊泡簇外。在用高k去极化时,在脱簇突触囊泡中散射克拉仑的标签,并将更靠近突触前的有源区移动。与轴突相比,Clathrin标记的CCV和CCP在休息条件下的SOMA /树枝状物中突出,并且在高k次去极化时变得不起眼。因此,EM检查表明,克拉辛介导的内吞作用的调节和机制在轴突和枝晶之间不同,并且在去极化时,克拉仑在这两个神经元隔室中再分分配。

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