| Literature DB >> 28817799 |
Steven A Sloan1, Spyros Darmanis2, Nina Huber3, Themasap A Khan3, Fikri Birey3, Christine Caneda1, Richard Reimer4, Stephen R Quake2, Ben A Barres1, Sergiu P Paşca5.
Abstract
There is significant need to develop physiologically relevant models for investigating human astrocytes in health and disease. Here, we present an approach for generating astrocyte lineage cells in a three-dimensional (3D) cytoarchitecture using human cerebral cortical spheroids (hCSs) derived from pluripotent stem cells. We acutely purified astrocyte-lineage cells from hCSs at varying stages up to 20 months in vitro using immunopanning and cell sorting and performed high-depth bulk and single-cell RNA sequencing to directly compare them to purified primary human brain cells. We found that hCS-derived glia closely resemble primary human fetal astrocytes and that, over time in vitro, they transition from a predominantly fetal to an increasingly mature astrocyte state. Transcriptional changes in astrocytes are accompanied by alterations in phagocytic capacity and effects on neuronal calcium signaling. These findings suggest that hCS-derived astrocytes closely resemble primary human astrocytes and can be used for studying development and modeling disease.Entities:
Keywords: RNA-seq; astrocyte; cerebral cortex; hCS; human; iPSC; maturation; organoids; spheroids; transcriptome
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Year: 2017 PMID: 28817799 PMCID: PMC5890820 DOI: 10.1016/j.neuron.2017.07.035
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173