Purification and characterization of human neural stem and progenitor cells

被引:38
|
作者
Liu, Daniel Dan [1 ]
He, Joy Q. [1 ]
Sinha, Rahul [1 ]
Eastman, Anna E. [1 ]
Toland, Angus M. [2 ]
Morri, Maurizio [3 ]
Neff, Norma F. [3 ]
Vogel, Hannes [2 ]
Uchida, Nobuko [1 ]
Weissman, Irving L. [1 ,2 ]
机构
[1] Stanford Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[2] Dept Pathol, Stanford Med, Stanford, CA 94305 USA
[3] Chan Zuckerberg Biohub, Stanford, CA 94305 USA
关键词
SUBVENTRICULAR ZONE; RADIAL GLIA; RNA-SEQ; DIFFERENTIATION; ASTROCYTE; FETAL;
D O I
10.1016/j.cell.2023.02.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human brain undergoes rapid development at mid-gestation from a pool of neural stem and progenitor cells (NSPCs) that give rise to the neurons, oligodendrocytes, and astrocytes of the mature brain. Functional study of these cell types has been hampered by a lack of precise purification methods. We describe a method for prospectively isolating ten distinct NSPC types from the developing human brain using cell-surface markers. CD24-THY1-/lo cells were enriched for radial glia, which robustly engrafted and differentiated into all three neural lineages in the mouse brain. THY1hi cells marked unipotent oligodendrocyte precursors committed to an oligodendroglial fate, and CD24+THY1-/lo cells marked committed excitatory and inhibitory neuronal lineages. Notably, we identify and functionally characterize a transcriptomically distinct THY1hiEGFRhiPDGFRA- bipotent glial progenitor cell (GPC), which is lineage-restricted to astrocytes and ol-igodendrocytes, but not to neurons. Our study provides a framework for the functional study of distinct cell types in human neurodevelopment.
引用
收藏
页码:1179 / +
页数:32
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