Bilateral and symmetric glycinergic and glutamatergic projections from the LSO to the IC in the CBA/CaH mouse

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Isabella R. Williams, D. Ryugo
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引用次数: 0

Abstract

Auditory space has been conceptualized as a matrix of systematically arranged combinations of binaural disparity cues that arise in the superior olivary complex (SOC). The computational code for interaural time and intensity differences utilizes excitatory and inhibitory projections that converge in the inferior colliculus (IC). The challenge is to determine the neural circuits underlying this convergence and to model how the binaural cues encode location. It has been shown that midbrain neurons are largely excited by sound from the contralateral ear and inhibited by sound leading at the ipsilateral ear. In this context, ascending projections from the lateral superior olive (LSO) to the IC have been reported to be ipsilaterally glycinergic and contralaterally glutamatergic. This study used CBA/CaH mice (3–6 months old) and applied unilateral retrograde tracing techniques into the IC in conjunction with immunocytochemical methods with glycine and glutamate transporters (GlyT2 and vGLUT2, respectively) to analyze the projection patterns from the LSO to the IC. Glycinergic and glutamatergic neurons were spatially intermixed within the LSO, and both types projected to the IC. For GlyT2 and vGLUT2 neurons, the average percentage of ipsilaterally and contralaterally projecting cells was similar (ANOVA, p = 0.48). A roughly equal number of GlyT2 and vGLUT2 neurons did not project to the IC. The somatic size and shape of these neurons match the descriptions of LSO principal cells. A minor but distinct population of small (< 40 μm2) neurons that labeled for GlyT2 did not project to the IC; these cells emerge as candidates for inhibitory local circuit neurons. Our findings indicate a symmetric and bilateral projection of glycine and glutamate neurons from the LSO to the IC. The differences between our results and those from previous studies suggest that species and habitat differences have a significant role in mechanisms of binaural processing and highlight the importance of research methods and comparative neuroscience. These data will be important for modeling how excitatory and inhibitory systems converge to create auditory space in the CBA/CaH mouse.
CBA/CaH小鼠从LSO到IC的双侧和对称甘氨酸能和谷氨酸能投射
听觉空间的概念是上橄榄复合体(SOC)中产生的双耳差异线索的系统排列组合矩阵。耳际时间和强度差异的计算代码利用的是在下丘(IC)汇聚的兴奋和抑制投射。目前的挑战是确定这种汇聚的神经回路,并对双耳线索如何编码位置进行建模。研究表明,中脑神经元在很大程度上会被对侧耳的声音所激发,而被同侧耳的声音所抑制。在这种情况下,据报道,从外侧上橄榄(LSO)到集成电路的上升投射是同侧的甘氨酸能和对侧的谷氨酸能。本研究使用 CBA/CaH 小鼠(3-6 个月大),结合甘氨酸和谷氨酸转运体(分别为 GlyT2 和 vGLUT2)的免疫细胞化学方法,应用单侧逆行追踪技术进入 IC,分析从 LSO 到 IC 的投射模式。甘氨酸能神经元和谷氨酸能神经元在空间上混杂在 LSO 中,两种类型的神经元都投射到 IC。对于 GlyT2 和 vGLUT2 神经元,同侧和对侧投射细胞的平均百分比相似(方差分析,p = 0.48)。大致相同数量的 GlyT2 和 vGLUT2 神经元没有向 IC 投射。这些神经元的体细胞大小和形状与 LSO 主细胞的描述相符。标记有 GlyT2 的小神经元(< 40 μm2)虽然数量不多,但却与众不同,它们没有投射到 IC;这些细胞是抑制性局部回路神经元的候选者。我们的研究结果表明,甘氨酸和谷氨酸神经元从 LSO 向 IC 的投射是对称和双侧的。我们的研究结果与以往研究结果之间的差异表明,物种和栖息地的差异在双耳加工机制中起着重要作用,并凸显了研究方法和比较神经科学的重要性。这些数据对于模拟兴奋和抑制系统如何在CBA/CaH小鼠中汇聚以创建听觉空间非常重要。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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