GFAP阴性原始神经干细胞及其子代在克隆分辨率下的命运鉴定。

IF 2.5 3区 医学 Q3 CELL & TISSUE ENGINEERING Stem cells and development Pub Date : 2023-10-01 Epub Date: 2023-09-11 DOI:10.1089/scd.2023.0038
Samantha Yammine, Ian Burns, Jessica Gosio, Andrew Peluso, Daniel Merritt, Brendan Innes, Brenda Coles, Wen Rui Yan, Gary D Bader, Cindi Morshead, Derek van der Kooy
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引用次数: 0

摘要

成熟的大脑含有数量惊人、种类繁多的细胞,这些细胞由异质的神经干细胞库(NSCs)产生和维持。在发育中和成年小鼠大脑中存在两种不同类型的神经干细胞:胶质纤维酸性蛋白(GFAP)阴性的原始(p)神经干细胞和下游GFAP阳性的最终(d)神经干细胞核。为了更好地了解NSCs的胚胎功能,我们在从pNSCs或dNSCs生长的神经球中进行了克隆谱系追踪,以富集其最直接的下游神经祖细胞(NPC)。这些克隆祖细胞谱系追踪数据使我们能够构建pNSCs和dNSCs下游祖细胞亚型的层次结构,然后使用单细胞转录组学对其进行验证。此外,我们从罕见pNSC下游的神经元/星形胶质细胞祖细胞中鉴定出Nexn是神经元规格所需的。综合起来,这些数据提供了罕见pNSC下游NPC谱系的单细胞分辨率,而体内群体水平分析可能会遗漏这些分辨率。
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Fate Specification of GFAP-Negative Primitive Neural Stem Cells and Their Progeny at Clonal Resolution.

The mature brain contains an incredible number and diversity of cells that are produced and maintained by heterogeneous pools of neural stem cells (NSCs). Two distinct types of NSCs exist in the developing and adult mouse brain: Glial Fibrillary Acidic Protein (GFAP)-negative primitive (p)NSCs and downstream GFAP-positive definitive (d)NSCs. To better understand the embryonic functions of NSCs, we performed clonal lineage tracing within neurospheres grown from either pNSCs or dNSCs to enrich for their most immediate downstream neural progenitor cells (NPCs). These clonal progenitor lineage tracing data allowed us to construct a hierarchy of progenitor subtypes downstream of pNSCs and dNSCs that were then validated using single-cell transcriptomics. Further, we identify Nexn as required for neuronal specification from neuron/astrocyte progenitor cells downstream of rare pNSCs. Combined, these data provide single-cell resolution of NPC lineages downstream of rare pNSCs that likely would be missed from population-level analyses in vivo.

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来源期刊
Stem cells and development
Stem cells and development 医学-细胞与组织工程
CiteScore
7.80
自引率
2.50%
发文量
69
审稿时长
3 months
期刊介绍: Stem Cells and Development is globally recognized as the trusted source for critical, even controversial coverage of emerging hypotheses and novel findings. With a focus on stem cells of all tissue types and their potential therapeutic applications, the Journal provides clinical, basic, and translational scientists with cutting-edge research and findings. Stem Cells and Development coverage includes: Embryogenesis and adult counterparts of this process Physical processes linking stem cells, primary cell function, and structural development Hypotheses exploring the relationship between genotype and phenotype Development of vasculature, CNS, and other germ layer development and defects Pluripotentiality of embryonic and somatic stem cells The role of genetic and epigenetic factors in development
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