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通过对小脑学习相关的脑干前庭神经元的单细胞表达谱进行分析,实现神经元分类和标记基因鉴定。

Neuronal classification and marker gene identification via single-cell expression profiling of brainstem vestibular neurons subserving cerebellar learning.

机构信息

Howard Hughes Medical Institute, Salk Institute for Biological Studies, La Jolla, California, 92037, USA.

出版信息

J Neurosci. 2012 Jun 6;32(23):7819-31. doi: 10.1523/JNEUROSCI.0543-12.2012.

Abstract

Identification of marker genes expressed in specific cell types is essential for the genetic dissection of neural circuits. Here we report a new strategy for classifying heterogeneous populations of neurons into functionally distinct types and for identifying associated marker genes. Quantitative single-cell expression profiling of genes related to neurotransmitters and ion channels enables functional classification of neurons; transcript profiles for marker gene candidates identify molecular handles for manipulating each cell type. We apply this strategy to the mouse medial vestibular nucleus (MVN), which comprises several types of neurons subserving cerebellar-dependent learning in the vestibulo-ocular reflex. Ion channel gene expression differed both qualitatively and quantitatively across cell types and could distinguish subtle differences in intrinsic electrophysiology. Single-cell transcript profiling of MVN neurons established six functionally distinct cell types and associated marker genes. This strategy is applicable throughout the nervous system and could facilitate the use of molecular genetic tools to examine the behavioral roles of distinct neuronal populations.

摘要

鉴定在特定细胞类型中表达的标记基因对于神经回路的遗传剖析至关重要。在这里,我们报告了一种新的策略,用于将异质神经元群体分类为功能不同的类型,并鉴定相关的标记基因。对与神经递质和离子通道相关的基因进行定量单细胞表达谱分析,可实现神经元的功能分类;标记基因候选物的转录谱可确定用于操纵每种细胞类型的分子把手。我们将这种策略应用于小鼠内侧前庭核 (MVN),其中包含几种神经元,它们在前庭眼反射中的小脑依赖学习中起作用。离子通道基因的表达在细胞类型之间既有定性差异,也有定量差异,并且可以区分内在电生理学的细微差异。MVN 神经元的单细胞转录谱确定了六个功能不同的细胞类型和相关的标记基因。这种策略适用于整个神经系统,并可以促进使用分子遗传工具来研究不同神经元群体的行为作用。

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