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单细胞RNA测序揭示的小鼠纹状体细胞分类学

Cellular Taxonomy of the Mouse Striatum as Revealed by Single-Cell RNA-Seq.

作者信息

Gokce Ozgun, Stanley Geoffrey M, Treutlein Barbara, Neff Norma F, Camp J Gray, Malenka Robert C, Rothwell Patrick E, Fuccillo Marc V, Südhof Thomas C, Quake Stephen R

机构信息

Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA; Institute for Stroke and Dementia Research, Klinikum der Universität München, Ludwig-Maximilians-Universität LMU, 81377 Munich, Germany.

Biophysics Program, Stanford University, Stanford, CA 94305, USA; Departments of Bioengineering and Applied Physics, Stanford University, Stanford, CA 94305, USA.

出版信息

Cell Rep. 2016 Jul 26;16(4):1126-1137. doi: 10.1016/j.celrep.2016.06.059. Epub 2016 Jul 14.

Abstract

The striatum contributes to many cognitive processes and disorders, but its cell types are incompletely characterized. We show that microfluidic and FACS-based single-cell RNA sequencing of mouse striatum provides a well-resolved classification of striatal cell type diversity. Transcriptome analysis revealed ten differentiated, distinct cell types, including neurons, astrocytes, oligodendrocytes, ependymal, immune, and vascular cells, and enabled the discovery of numerous marker genes. Furthermore, we identified two discrete subtypes of medium spiny neurons (MSNs) that have specific markers and that overexpress genes linked to cognitive disorders and addiction. We also describe continuous cellular identities, which increase heterogeneity within discrete cell types. Finally, we identified cell type-specific transcription and splicing factors that shape cellular identities by regulating splicing and expression patterns. Our findings suggest that functional diversity within a complex tissue arises from a small number of discrete cell types, which can exist in a continuous spectrum of functional states.

摘要

纹状体参与许多认知过程和疾病,但它的细胞类型尚未完全明确。我们表明,基于微流控和荧光激活细胞分选技术的小鼠纹状体单细胞RNA测序能够很好地解析纹状体细胞类型的多样性。转录组分析揭示了十种分化的、不同的细胞类型,包括神经元、星形胶质细胞、少突胶质细胞、室管膜细胞、免疫细胞和血管细胞,并发现了许多标记基因。此外,我们确定了中型多棘神经元(MSN)的两种离散亚型,它们具有特定的标记,并且过度表达与认知障碍和成瘾相关的基因。我们还描述了连续的细胞身份,这增加了离散细胞类型内的异质性。最后,我们确定了细胞类型特异性的转录和剪接因子,它们通过调节剪接和表达模式来塑造细胞身份。我们的研究结果表明,复杂组织中的功能多样性源于少数离散的细胞类型,这些细胞类型可以存在于连续的功能状态谱中。

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