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鸡大细胞神经核神经元的膜和突触特性的音频拓扑梯度

Tonotopic gradients of membrane and synaptic properties for neurons of the chicken nucleus magnocellularis.

作者信息

Fukui Iwao, Ohmori Harunori

机构信息

Department of Physiology, Faculty of Medicine, Kyoto University, Kyoto 606-8501, Japan.

出版信息

J Neurosci. 2004 Aug 25;24(34):7514-23. doi: 10.1523/JNEUROSCI.0566-04.2004.

Abstract

Nucleus magnocellularis (NM) is a division of the avian cochlear nucleus that extracts the timing of auditory signals. We compared the membrane excitability and synaptic transmission along the tonotopic axis of NM. Neurons expressed a Kv1.1 potassium channel mRNA and protein predominantly in the high characteristic frequency (CF) region of NM. In contrast, the expression of Kv1.2 mRNA did not change tonotopically. Neurons also showed tonotopic gradients in resting potential, spike threshold, amplitude, and membrane rectification. All neurons were sensitive to 100 nm dendrotoxin, but the effects were most significant in the high CF neurons. The EPSC recorded by minimal stimulation of auditory nerve fibers (ANFs) was 13 times larger in high CF neurons than in low CF neurons. Moreover, EPSCs were generated in an all-or-none manner in the high CF neurons when stimulus intensity was increased, whereas EPSCs were graded in the low CF neurons, indicating multiple axonal inputs. ANF synaptic terminals were visualized by DiI. ANF formed enfolding end-bulbs of Held around the cell body in the high and middle CF region but not in the low CF region. These observations indicate coordinated gradients of neuronal properties both presynaptically and postsynaptically along the tonotopic axis. Such specializations may be suitable for extracting and preserving the timing information of auditory signals over a wide range of acoustic frequencies.

摘要

巨细胞核(NM)是禽耳蜗核的一个分区,负责提取听觉信号的时间信息。我们比较了NM沿音频拓扑轴的膜兴奋性和突触传递。神经元主要在NM的高特征频率(CF)区域表达Kv1.1钾通道mRNA和蛋白。相比之下,Kv1.2 mRNA的表达没有音频拓扑变化。神经元在静息电位、动作电位阈值、幅度和膜整流方面也表现出音频拓扑梯度。所有神经元对100 nM树突毒素敏感,但在高CF神经元中效应最为显著。通过最小刺激听觉神经纤维(ANF)记录的兴奋性突触后电流(EPSC)在高CF神经元中比在低CF神经元中大13倍。此外,当刺激强度增加时,高CF神经元中的EPSC以全或无的方式产生,而低CF神经元中的EPSC是分级的,表明存在多个轴突输入。通过DiI可视化ANF突触终末。在高CF和中CF区域,ANF在细胞体周围形成包围型Held终球,但在低CF区域则没有。这些观察结果表明,沿音频拓扑轴在突触前和突触后神经元特性存在协同梯度。这种特化可能适用于在广泛的声频范围内提取和保存听觉信号的时间信息。

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