Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq

被引:2108
作者
Zeisel, Amit [1 ]
Munoz-Manchado, Ana B. [1 ]
Codeluppi, Simone [1 ]
Lonnerberg, Peter [1 ]
La Manno, Gioele [1 ]
Jureus, Anna [1 ]
Marques, Sueli [1 ]
Munguba, Hermany [1 ]
He, Liqun [2 ]
Betsholtz, Christer [2 ,3 ]
Rolny, Charlotte [4 ]
Castelo-Branco, Goncalo [1 ]
Hjerling-Leffler, Jens [1 ]
Linnarsson, Sten [1 ]
机构
[1] Karolinska Inst, Dept Med Biochem & Biophys, Div Mol Neurobiol, S-17177 Stockholm, Sweden
[2] Uppsala Univ, Rudbeck Lab, Dept Immunol Genet & Pathol, S-75185 Uppsala, Sweden
[3] Karolinska Inst, Div Vasc Biol, Dept Med Biochem & Biophys, S-17177 Stockholm, Sweden
[4] Karolinska Inst, Dept Oncol Pathol, S-17176 Stockholm, Sweden
基金
欧洲研究理事会; 瑞典研究理事会;
关键词
CEREBRAL-CORTEX; MACROPHAGES; EXPRESSION; BRAIN; STEP; CA1;
D O I
10.1126/science.aaa1934
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mammalian cerebral cortex supports cognitive functions such as sensorimotor integration, memory, and social behaviors. Normal brain function relies on a diverse set of differentiated cell types, including neurons, glia, and vasculature. Here, we have used large-scale single-cell RNA sequencing (RNA-seq) to classify cells in the mouse somatosensory cortex and hippocampal CA1 region. We found 47 molecularly distinct subclasses, comprising all known major cell types in the cortex. We identified numerous marker genes, which allowed alignment with known cell types, morphology, and location. We found a layer I interneuron expressing Pax6 and a distinct postmitotic oligodendrocyte subclass marked by Itpr2. Across the diversity of cortical cell types, transcription factors formed a complex, layered regulatory code, suggesting a mechanism for the maintenance of adult cell type identity.
引用
收藏
页码:1138 / 1142
页数:5
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