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使用蓝光和红移通道视紫红质对下丘神经元进行远程通道视紫红质辅助电路映射

Long-range Channelrhodopsin-assisted Circuit Mapping of Inferior Colliculus Neurons with Blue and Red-shifted Channelrhodopsins.

作者信息

Goyer David, Roberts Michael T

机构信息

Kresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, University of Michigan.

Kresge Hearing Research Institute, Department of Otolaryngology - Head and Neck Surgery, University of Michigan;

出版信息

J Vis Exp. 2020 Feb 7(156). doi: 10.3791/60760.

Abstract

When investigating neural circuits, a standard limitation of the in vitro patch clamp approach is that axons from multiple sources are often intermixed, making it difficult to isolate inputs from individual sources with electrical stimulation. However, by using channelrhodopsin assisted circuit mapping (CRACM), this limitation can now be overcome. Here, we report a method to use CRACM to map ascending inputs from lower auditory brainstem nuclei and commissural inputs to an identified class of neurons in the inferior colliculus (IC), the midbrain nucleus of the auditory system. In the IC, local, commissural, ascending, and descending axons are heavily intertwined and therefore indistinguishable with electrical stimulation. By injecting a viral construct to drive expression of a channelrhodopsin in a presynaptic nucleus, followed by patch clamp recording to characterize the presence and physiology of channelrhodopsin-expressing synaptic inputs, projections from a specific source to a specific population of IC neurons can be mapped with cell type-specific accuracy. We show that this approach works with both Chronos, a blue light-activated channelrhodopsin, and ChrimsonR, a red-shifted channelrhodopsin. In contrast to previous reports from the forebrain, we find that ChrimsonR is robustly trafficked down the axons of dorsal cochlear nucleus principal neurons, indicating that ChrimsonR may be a useful tool for CRACM experiments in the brainstem. The protocol presented here includes detailed descriptions of the intracranial virus injection surgery, including stereotaxic coordinates for targeting injections to the dorsal cochlear nucleus and IC of mice, and how to combine whole cell patch clamp recording with channelrhodopsin activation to investigate long-range projections to IC neurons. Although this protocol is tailored to characterizing auditory inputs to the IC, it can be easily adapted to investigate other long-range projections in the auditory brainstem and beyond.

摘要

在研究神经回路时,体外膜片钳方法的一个标准局限性在于,来自多个来源的轴突常常相互混杂,这使得通过电刺激分离来自单个来源的输入变得困难。然而,通过使用通道视紫红质辅助回路映射(CRACM),现在可以克服这一局限性。在这里,我们报告一种方法,利用CRACM来映射来自低位听觉脑干核的上行输入以及到下丘(IC)中一类已确定神经元的连合输入,IC是听觉系统的中脑核。在IC中,局部、连合、上行和下行轴突紧密交织,因此通过电刺激无法区分。通过在突触前核中注射病毒构建体以驱动通道视紫红质的表达,随后进行膜片钳记录以表征表达通道视紫红质的突触输入的存在和生理学特性,可以以细胞类型特异性的精度映射从特定来源到特定IC神经元群体的投射。我们表明,这种方法适用于蓝光激活的通道视紫红质Chronos和红移通道视紫红质ChrimsonR。与先前来自前脑的报道不同,我们发现ChrimsonR能强有力地沿着蜗背侧核主神经元的轴突运输,这表明ChrimsonR可能是脑干中CRACM实验的一个有用工具。这里介绍的方案包括颅内病毒注射手术的详细描述,包括靶向注射到小鼠蜗背侧核和IC的立体定位坐标,以及如何将全细胞膜片钳记录与通道视紫红质激活相结合来研究到IC神经元的长程投射。尽管该方案是为表征到IC的听觉输入量身定制的,但它可以很容易地适用于研究听觉脑干及其他部位的其他长程投射。

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