Single-Cell Transcriptomic Analysis Defines Heterogeneity and Transcriptional Dynamics in the Adult Neural Stem Cell Lineage

被引:244
|
作者
Dulken, Ben W. [1 ,2 ,3 ]
Leeman, Dena S. [1 ,4 ]
Boutet, Stephane C. [5 ]
Hebestreit, Katja [1 ]
Brunet, Anne [1 ,6 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Stanford Med Scientist Training Program, Stanford, CA 94305 USA
[3] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[4] Stanford Univ, Canc Biol Program, Stanford, CA 94305 USA
[5] Fluidigm Corp, San Francisco, CA 94080 USA
[6] Stanford Univ, Glenn Labs Biol Aging, Stanford, CA 94305 USA
来源
CELL REPORTS | 2017年 / 18卷 / 03期
关键词
SUBVENTRICULAR ZONE; SELF-RENEWAL; EXPRESSION ANALYSIS; SUBEPENDYMAL ZONE; RNA-SEQ; REVEALS; BRAIN; NEUROGENESIS; ASTROCYTES; SIGNALS;
D O I
10.1016/j.celrep.2016.12.060
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neural stem cells (NSCs) in the adult mammalian brain serve as a reservoir for the generation of new neurons, oligodendrocytes, and astrocytes. Here, we use single-cell RNA sequencing to characterize adult NSC populations and examine the molecular identities and heterogeneity of in vivo NSC populations. We find that cells in the NSC lineage exist on a continuum through the processes of activation and differentiation. Interestingly, rare intermediate states with distinct molecular profiles can be identified and experimentally validated, and our analysis identifies putative surface markers and key intracellular regulators for these subpopulations of NSCs. Finally, using the power of single-cell profiling, we conduct a meta-analysis to compare in vivo NSCs and in vitro cultures, distinct fluorescence-activated cell sorting strategies, and different neurogenic niches. These data provide a resource for the field and contribute to an integrative understanding of the adult NSC lineage.
引用
收藏
页码:777 / 790
页数:14
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