| Literature DB >> 32234482 |
Yue Zhang1, Guoping Liu2, Teng Guo2, Xiaoyi G Liang1, Heng Du2, Lin Yang2, Aparna Bhaduri3, Xiaosu Li2, Zhejun Xu2, Zhuangzhi Zhang2, Zhenmeiyu Li2, Miao He2, Jeremiah Tsyporin1, Arnold R Kriegstein3, John L Rubenstein4, Zhengang Yang5, Bin Chen6.
Abstract
Neural stem cells (NSCs) in the prenatal neocortex progressively generate different subtypes of glutamatergic projection neurons. Following that, NSCs have a major switch in their progenitor properties and produce γ-aminobutyric acid (GABAergic) interneurons for the olfactory bulb (OB), cortical oligodendrocytes, and astrocytes. Herein, we provide evidence for the molecular mechanism that underlies this switch in the state of neocortical NSCs. We show that, at around E16.5, mouse neocortical NSCs start to generate GSX2-expressing (GSX2+) intermediate progenitor cells (IPCs). In vivo lineage-tracing study revealed that GSX2+ IPC population gives rise not only to OB interneurons but also to cortical oligodendrocytes and astrocytes, suggesting that they are a tri-potential population. We demonstrated that Sonic hedgehog signaling is both necessary and sufficient for the generation of GSX2+ IPCs by reducing GLI3R protein levels. Using single-cell RNA sequencing, we identify the transcriptional profile of GSX2+ IPCs and the process of the lineage switch of cortical NSCs.Entities:
Keywords: Gli3; Gsx2; Shh; cerebral cortex; neural stem cells; olfactory bulb interneurons; oligodendrocytes
Year: 2020 PMID: 32234482 DOI: 10.1016/j.celrep.2020.03.027
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423