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Humanized neuronal chimeric mouse brain generated by neonatally engrafted human iPSC-derived primitive neural progenitor cells
Chen Chen, … , Woo-Yang Kim, Peng Jiang
Chen Chen, … , Woo-Yang Kim, Peng Jiang
Published November 17, 2016
Citation Information: JCI Insight. 2016;1(19):e88632. https://doi.org/10.1172/jci.insight.88632.
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Research Article Neuroscience Stem cells

Humanized neuronal chimeric mouse brain generated by neonatally engrafted human iPSC-derived primitive neural progenitor cells

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Abstract

The creation of a humanized chimeric mouse nervous system permits the study of human neural development and disease pathogenesis using human cells in vivo. Humanized glial chimeric mice with the brain and spinal cord being colonized by human glial cells have been successfully generated. However, generation of humanized chimeric mouse brains repopulated by human neurons to possess a high degree of chimerism have not been well studied. Here we created humanized neuronal chimeric mouse brains by neonatally engrafting the distinct and highly neurogenic human induced pluripotent stem cell (hiPSC)–derived rosette-type primitive neural progenitors. These neural progenitors predominantly differentiate to neurons, which disperse widely throughout the mouse brain with infiltration of the cerebral cortex and hippocampus at 6 and 13 months after transplantation. Building upon the hiPSC technology, we propose that this potentially unique humanized neuronal chimeric mouse model will provide profound opportunities to define the structure, function, and plasticity of neural networks containing human neurons derived from a broad variety of neurological disorders.

Authors

Chen Chen, Woo-Yang Kim, Peng Jiang

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Figure 4

Astroglial differentiation of neonatally engrafted hiPSC-pNPCs.

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Astroglial differentiation of neonatally engrafted hiPSC-pNPCs.
(A) Repr...
(A) Representative images of glial fibrillary acidic protein–expressing (GFAP-expressing) astroglia in the human nuclear antigen–positive (hN+) cells near the injection site at 3 weeks after transplantation, and in the corpus callosum (CC), striatum (STR), and cerebral cortex (CTX) at 6 and 13 months after transplantation. Arrowheads indicate the hN+/GFAP+ human astroglia, and arrows indicate the hN–/GFAP+ endogenous host astroglia. Scale bars: 50 μm. The dotted lines highlight the CC region. (B) Representative image showing colocalization of hN and GFAP, and the long and tortuous processes of human astroglia in the mouse brain. (C) The percentage of GFAP-expressing cells in the hN+ cells at different brain regions from 3 weeks to 13 months (n = 6 for each time point). All quantitative data are analyses of pooled data collected from transplantation of hiPSC1- and hiPSC2-pNPCs. Data are presented as box-and-whisker plots. The central horizontal bars indicate the medians, boxes indicate 25th to 75th percentiles, and whiskers indicate the range of the data points. Student’s t tests and 1-way ANOVA were performed to assess the significance. **P < 0.01 and ***P < 0.001. hiPSC-pNPCs, human induced pluripotent stem cell–derived primitive neural progenitor cells.

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