Department of Otolaryngology/Head and Neck Surgery, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Department of Otolaryngology, The Ohio State University, Columbus, Ohio, United States of America.
PLoS One. 2019 Oct 3;14(10):e0223137. doi: 10.1371/journal.pone.0223137. eCollection 2019.
The cochlear nucleus (CN) transforms the spike trains of spiral ganglion cells into a set of sensory representations that are essential for auditory discriminations and perception. These transformations require the coordinated activity of different classes of neurons that are embryologically derived from distinct sets of precursors. Decades of investigation have shown that the neurons of the CN are differentiated by their morphology, neurotransmitter receptors, ion channel expression and intrinsic excitability. In the present study we have used linear discriminant analysis (LDA) to perform an unbiased analysis of measures of the responses of CN neurons to current injections to objectively categorize cells on the basis of both morphology and physiology. Recordings were made from cells in brain slices from CBA/CaJ mice and a transgenic mouse line, NF107, crossed against the Ai32 line. For each cell, responses to current injections were analyzed for spike rate, spike shape, input resistance, resting membrane potential, membrane time constant, hyperpolarization-activated sag and time constant. Cells were filled with dye for morphological classification, and visually classified according to published accounts. The different morphological classes of cells were separated with the LDA. Ventral cochlear nucleus (VCN) bushy cells, planar multipolar (T-stellate) cells, and radiate multipolar (D-stellate) cells were in separate clusters and separate from all of the neurons from the dorsal cochlear nucleus (DCN). Within the DCN, the pyramidal cells and tuberculoventral cells were largely separated from a distinct cluster of cartwheel cells. principal axes, whereas VCN cells were in 3 clouds approximately orthogonal to this plane. VCN neurons from the two mouse strains overlapped but were slightly separated, indicating either a strain dependence or differences in slice preparation methods. We conclude that cochlear nucleus neurons can be objectively distinguished based on their intrinsic electrical properties, but such distinctions are still best aided by morphological identification.
耳蜗核(CN)将螺旋神经节细胞的尖峰列车转换为一组感觉表示,这些表示对于听觉辨别和感知至关重要。这些转换需要不同类别的神经元的协调活动,这些神经元在胚胎发生上是由不同的前体细胞衍生而来的。几十年的研究表明,CN 的神经元通过其形态、神经递质受体、离子通道表达和内在兴奋性来区分。在本研究中,我们使用线性判别分析(LDA)对 CN 神经元对电流注入的反应进行了无偏分析,以便根据形态和生理学客观地对细胞进行分类。记录来自 CBA/CaJ 小鼠和 NF107 转基因小鼠系的脑片细胞,该系与 Ai32 系杂交。对于每个细胞,分析了电流注入引起的尖峰率、尖峰形状、输入电阻、静息膜电位、膜时间常数、超极化激活凹陷和时间常数的反应。用染料对细胞进行形态分类,并根据已发表的报道进行视觉分类。用 LDA 分离不同的形态细胞类群。耳蜗腹核(VCN)的毛细胞、平面多极(T 形)细胞和放射多极(D 形)细胞分别位于不同的簇中,与来自耳蜗背核(DCN)的所有神经元分开。在 DCN 中,锥体细胞和结节腹侧细胞主要与一个独特的轮状细胞簇分开。主要轴,而 VCN 细胞位于与该平面大致正交的 3 个云中。来自两种小鼠品系的 VCN 神经元重叠但略有分离,这表明存在品系依赖性或切片制备方法的差异。我们得出结论,耳蜗核神经元可以根据其内在电特性进行客观区分,但这种区分仍然最好通过形态识别来辅助。