Suppressing the DSCAM/PAK1 pathway reverses neurogenesis deficits in Down Syndrome patient iPSC-derived cerebral organoids

Down syndrome (DS), caused by trisomy of chromosome 21, occurs in 1 of every 800 live births. Early defects in cortical development likely account for the cognitive impairments in DS, although the underlying molecular mechanism remains elusive. Here, we performed histological assays and unbiased sin...

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Bibliographic Details
Published inThe Journal of clinical investigation
Main Authors Tang, Xiao-Yan, Xu, Lei, Wang, Jingshen, Hong, Yuan, Wang, Yuanyuan, Zhu, Qian, Wang, Da, Zhang, Xin-Yue, Liu, Chun-Yue, Fang, Kai-Heng, Han, Xiao, Wang, Shihua, Wang, Xin, Xu, Min, Bhattacharyya, Anita, Guo, Xing, Lin, Mingyan, Liu, Yan
Format Journal Article
LanguageEnglish
Published United States 04.05.2021
Subjects
Neuroscience
Stem cells
Neurodevelopment
Embryonic stem cells
iPS cells
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Summary:Down syndrome (DS), caused by trisomy of chromosome 21, occurs in 1 of every 800 live births. Early defects in cortical development likely account for the cognitive impairments in DS, although the underlying molecular mechanism remains elusive. Here, we performed histological assays and unbiased single-cell RNA sequencing (scRNA-seq) analysis on cerebral organoids derived from four euploid cell lines and from induced pluripotent stem cells (iPSCs) from three individuals with trisomy 21 to explore cell type-specific abnormalities associated with DS during early brain development. We found that neurogenesis was significantly affected based on diminished proliferation and decreased expression of layer II and IV markers in cortical neurons in the subcortical regions; this may be responsible for the reduced size of the organoids. Furthermore, suppression of the DSCAM-PAK1 pathway which showed enhanced activities in DS) via CRISPR/Cas9, CRISPRi or small-molecule inhibitor treatment reverses abnormal neurogenesis, thereby increasing the size of organoids derived from DS iPSCs. Our study demonstrated that 3D cortical organoids developed in vitro are a valuable model of DS and provided a direct link between dysregulation of the DSCAM-PAK1 pathway and developmental brain defects in DS.
ISSN:1558-8238