1型螺旋神经节神经元亚型向耳蜗前腹侧核主神经元的收敛。

IF 4.4 2区 医学 Q1 NEUROSCIENCES
Nicole F Wong, Sydney E Brongo, Evan A Forero, Shuohao Sun, Connor J Cook, Amanda M Lauer, Ulrich Müller, Matthew A Xu-Friedman
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引用次数: 0

摘要

哺乳动物的听觉系统通过螺旋神经节神经元(SGN)的亚型对声音进行编码,这些亚型对声级的敏感度不同,因此可以分辨出各种不同的声级。最新研究表明,生理上定义的 SGN 亚型至少对应三种分子亚型。目前还不清楚不同亚型的信息如何在耳蜗核内汇聚。我们使用转基因雌雄小鼠研究了这一问题,这些小鼠在对其中两种亚型的标记物呈阳性的 SGN 中表达 Cre 重组酶:1a型SGN中的CALB2(钙视蛋白)和1c型SGN中的LYPD1分别对应于高敏感亚型和低敏感亚型。我们将这些小鼠与表达floxxed channelrhodopsin的小鼠杂交,这样就能利用光遗传学特异性地激活来自1a型或1c型SGN的轴突。我们对耳蜗前腹核(AVCN)的丛细胞进行了电压钳记录,发现CALB2-和LYPD1阳性SGN形成的突触具有相似的EPSC振幅和短期可塑性。免疫组化显示,单个丛状细胞接受 1a、1b 和 1c 突触的混合,其 VGluT1 阳性点的大小相似。在体内记录过程中,我们使用光遗传刺激将斩波单元和类初等单元分为接受与不接受 1a 型或 1c 型输入的两组。这两组在阈值或自发率上没有明显差异,表明亚型并没有在AVCN中分离成不同的处理流。我们的研究结果表明,AVCN 中的主细胞整合了来自所有 SGN 亚型的信息,具有广泛的趋同性,可在较大的动态范围内优化声音编码。听觉传入分为三个亚型,它们的自发活动和声音诱发活动各不相同。这些亚型可通过解剖、生理和分子特征加以区分。然而,人们对这三种亚型如何向大脑传递信息还不甚了解。我们利用光遗传刺激来研究耳蜗核前腹部两个传入亚型的特性,从而解决了这一问题。我们发现,不同亚型之间的突触特性并无差别,而且它们表现出广泛的趋同性,这表明结合不同声级敏感度的输入对处理声音非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Convergence of Type 1 Spiral Ganglion Neuron Subtypes onto Principal Neurons of the Anteroventral Cochlear Nucleus.

The mammalian auditory system encodes sounds with subtypes of spiral ganglion neurons (SGNs) that differ in sound level sensitivity, permitting discrimination across a wide range of levels. Recent work suggests the physiologically defined SGN subtypes correspond to at least three molecular subtypes. It is not known how information from the different subtypes converges within the cochlear nucleus. We examined this issue using transgenic mice of both sexes that express Cre recombinase in SGNs that are positive for markers of two subtypes: CALB2 (calretinin) in type 1a SGNs and LYPD1 in type 1c SGNs, which correspond to high- and low-sensitivity subtypes, respectively. We crossed these with mice expressing floxed channelrhodopsin, which allowed specific activation of axons from type 1a or 1c SGNs using optogenetics. We made voltage-clamp recordings from bushy cells in the anteroventral cochlear nucleus (AVCN) and found that the synapses formed by CALB2- and LYPD1-positive SGNs had similar EPSC amplitudes and short-term plasticity. Immunohistochemistry revealed that individual bushy cells receive a mix of 1a, 1b, and 1c synapses with VGluT1-positive puncta of similar sizes. We used optogenetic stimulation during in vivo recordings to classify chopper and primary-like units as receiving versus nonreceiving 1a- or 1c-type inputs. These groups showed no significant difference in threshold or spontaneous rate, suggesting the subtypes do not segregate into distinct processing streams in the AVCN. Our results indicate that principal cells in the AVCN integrate information from all SGN subtypes with extensive convergence, which could optimize sound encoding across a large dynamic range.

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来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
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