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体内钙离子成像显示树突兴奋性降低导致惊吓习惯化。

In Vivo Ca(2+) Imaging Reveals that Decreased Dendritic Excitability Drives Startle Habituation.

作者信息

Marsden Kurt C, Granato Michael

机构信息

Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

出版信息

Cell Rep. 2015 Dec 1;13(9):1733-40. doi: 10.1016/j.celrep.2015.10.060. Epub 2015 Nov 19.

Abstract

Exposure to repetitive startling stimuli induces habitation, a simple form of learning. Despite its simplicity, the precise cellular mechanisms by which repeated stimulation converts a robust behavioral response to behavioral indifference are unclear. Here, we use head-restrained zebrafish larvae to monitor subcellular Ca(2+) dynamics in Mauthner neurons, the startle command neurons, during startle habituation in vivo. Using the Ca(2+) reporter GCaMP6s, we find that the amplitude of Ca(2+) signals in the lateral dendrite of the Mauthner neuron determines startle probability and that depression of this dendritic activity rather than downstream inhibition mediates glycine and N-methyl-D-aspartate (NMDA)-receptor-dependent short-term habituation. Combined, our results suggest a model for habituation learning in which increased inhibitory drive from feedforward inhibitory neurons combined with decreased excitatory input from auditory afferents decreases dendritic and Mauthner neuron excitability.

摘要

暴露于重复性惊吓刺激会引发习惯化,这是一种简单的学习形式。尽管其简单,但重复刺激将强烈的行为反应转变为行为冷漠的确切细胞机制尚不清楚。在此,我们使用头部固定的斑马鱼幼体来监测体内惊吓习惯化过程中,作为惊吓指令神经元的毛特纳神经元的亚细胞钙(Ca(2+))动态变化。使用钙(Ca(2+))报告基因GCaMP6s,我们发现毛特纳神经元外侧树突中的钙(Ca(2+))信号幅度决定了惊吓概率,并且这种树突活动的抑制而非下游抑制介导了甘氨酸和N-甲基-D-天冬氨酸(NMDA)受体依赖性短期习惯化。综合来看,我们的结果提出了一种习惯化学习模型,其中来自前馈抑制性神经元的抑制驱动增加,与来自听觉传入神经的兴奋性输入减少相结合,降低了树突和毛特纳神经元的兴奋性。

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