Shiju Gu, Anastasios V Tzingounis, George Lykotrafitis
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引用次数: 0
Abstract
Small-conductance calcium-activated potassium (SK) channels show a ubiquitous distribution on neurons, in both somatodendritic and axonal regions. SK channels are associated with neuronal activity regulating action potential frequency, dendritic excitability, and synaptic plasticity. Although the physiology of SK channels and the mechanisms that control their surface expression levels have been investigated extensively, little is known about what controls SK channel diffusion in the neuronal plasma membrane. This aspect is important, as the diffusion of SK channels at the surface may control their localization and proximity to calcium channels, hence increasing the likelihood of SK channel activation by calcium. In this study, we successfully investigated the diffusion of SK channels labeled with quantum dots on human embryonic kidney cells and dissociated hippocampal neurons by combining a single-particle tracking method with total internal reflection fluorescence microscopy. We observed that actin filaments interfere with SK mobility, decreasing their diffusion coefficient. We also found that during neuronal maturation, SK channel diffusion was gradually inhibited in somatodendritic compartments. Importantly, we observed that axon barriers formed at approximately days in vitro 6 and restricted the diffusion of SK channels on the axon initial segment (AIS). However, after neuron maturation, SK channels on the AIS were strongly immobilized, even after disruption of the actin network, suggesting that crowding may cause this effect. Altogether, our work provides insight into how SK channels diffuse on the neuronal plasma membrane and how actin and membrane crowding impacts SK channel diffusion.
小传导钙激活钾(SK)通道在神经元上无处不在,既分布在体突区域,也分布在轴突区域。SK 通道与调节动作电位频率、树突兴奋性和突触可塑性的神经元活动有关。尽管对 SK 通道的生理学和控制其表面表达水平的机制进行了广泛研究,但人们对 SK 通道在神经元质膜中的扩散受什么因素控制却知之甚少。这方面的研究非常重要,因为 SK 通道在表面的扩散可能会控制它们的定位和与钙通道的接近程度,从而增加 SK 通道被钙激活的可能性。在这项研究中,我们结合单粒子跟踪法和全内反射荧光显微镜,成功地研究了用量子点标记的 SK 通道在人胚肾细胞和离体海马神经元上的扩散情况。我们观察到肌动蛋白丝干扰了 SK 的移动,降低了其扩散系数。我们还发现,在神经元成熟过程中,体支树突区的 SK 通道扩散逐渐受到抑制。重要的是,我们观察到轴突屏障在体外 6 天左右形成,并限制了 SK 通道在轴突初始节段(AIS)上的扩散。然而,在神经元成熟后,即使肌动蛋白网络被破坏,轴突初段上的 SK 通道也会被强烈固定,这表明拥挤可能会导致这种效应。总之,我们的工作让我们深入了解了 SK 通道如何在神经元质膜上扩散,以及肌动蛋白和膜拥挤如何影响 SK 通道的扩散。