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活动状态、轴突投射和位置的变化定义了单个新皮层投射神经元的转录特征。

Variation in Activity State, Axonal Projection, and Position Define the Transcriptional Identity of Individual Neocortical Projection Neurons.

机构信息

Biochemistry, Cellular and Molecular Biology Graduate Program, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

Human Genetics Training Program, McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Cell Rep. 2018 Jan 9;22(2):441-455. doi: 10.1016/j.celrep.2017.12.046.

Abstract

Single-cell RNA sequencing has generated catalogs of transcriptionally defined neuronal subtypes of the brain. However, the cellular processes that contribute to neuronal subtype specification and transcriptional heterogeneity remain unclear. By comparing the gene expression profiles of single layer 6 corticothalamic neurons in somatosensory cortex, we show that transcriptional subtypes primarily reflect axonal projection pattern, laminar position within the cortex, and neuronal activity state. Pseudotemporal ordering of 1,023 cellular responses to sensory manipulation demonstrates that changes in expression of activity-induced genes both reinforced cell-type identity and contributed to increased transcriptional heterogeneity within each cell type. This is due to cell-type biased choices of transcriptional states following manipulation of neuronal activity. These results reveal that axonal projection pattern, laminar position, and activity state define significant axes of variation that contribute both to the transcriptional identity of individual neurons and to the transcriptional heterogeneity within each neuronal subtype.

摘要

单细胞 RNA 测序已经生成了大脑中转录定义的神经元亚型目录。然而,对于导致神经元亚型特化和转录异质性的细胞过程仍不清楚。通过比较感觉皮层中 6 层皮质丘脑神经元的基因表达谱,我们表明转录亚型主要反映轴突投射模式、皮层内的层位置和神经元活动状态。1023 个对感觉处理反应的细胞的拟时排序表明,活性诱导基因表达的变化既增强了细胞类型的特征,又增加了每个细胞类型内的转录异质性。这是由于在神经元活动操作后,细胞类型偏向于选择转录状态。这些结果表明,轴突投射模式、层位置和活动状态定义了重要的变化轴,这些变化轴既有助于单个神经元的转录特征,也有助于每个神经元亚型内的转录异质性。

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