共 69 条
Cellular Taxonomy of the Mouse Striatum as Revealed by Single-Cell RNA-Seq
被引:315
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Stanley, Geoffrey M.
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Stanford Univ, Biophys Program, Stanford, CA 94305 USA
Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

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Camp, J. Gray
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Max Planck Inst Evolutionary Anthropol, Dept Evolutionary Genet, Deutsch Pl 6, D-04103 Leipzig, Germany Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Malenka, Robert C.
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Stanford Univ, Nancy Pritzker Lab, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Rothwell, Patrick E.
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Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
Stanford Univ, Nancy Pritzker Lab, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Fuccillo, Marc V.
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Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
Stanford Univ, Nancy Pritzker Lab, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Sudhof, Thomas C.
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Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA

Quake, Stephen R.
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Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
机构:
[1] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] Stanford Univ, Biophys Program, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[5] Stanford Univ, Nancy Pritzker Lab, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[6] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[7] Max Planck Inst Evolutionary Anthropol, Dept Evolutionary Genet, Deutsch Pl 6, D-04103 Leipzig, Germany
[8] Univ Munich, Klinikum Univ Munchen, Inst Stroke & Dementia Res, D-81377 Munich, Germany
关键词:
GENOME-WIDE ASSOCIATION;
BASAL GANGLIA FUNCTION;
INDIRECT PATHWAYS;
DIRECT CONVERSION;
STEM-CELLS;
EXPRESSION;
IDENTIFICATION;
RECEPTORS;
TRANSCRIPTOME;
NEURONS;
D O I:
10.1016/j.celrep.2016.06.059
中图分类号:
Q2 [细胞生物学];
学科分类号:
071013 [干细胞生物学];
摘要:
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.
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页码:1126 / 1137
页数:12
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