Hallmarks of Alzheimer's Disease in Stem-Cell-Derived Human Neurons Transplanted into Mouse Brain
- PMID: 28238547
- DOI: 10.1016/j.neuron.2017.02.001
Hallmarks of Alzheimer's Disease in Stem-Cell-Derived Human Neurons Transplanted into Mouse Brain
Abstract
Human pluripotent stem cells (PSCs) provide a unique entry to study species-specific aspects of human disorders such as Alzheimer's disease (AD). However, in vitro culture of neurons deprives them of their natural environment. Here we transplanted human PSC-derived cortical neuronal precursors into the brain of a murine AD model. Human neurons differentiate and integrate into the brain, express 3R/4R Tau splice forms, show abnormal phosphorylation and conformational Tau changes, and undergo neurodegeneration. Remarkably, cell death was dissociated from tangle formation in this natural 3D model of AD. Using genome-wide expression analysis, we observed upregulation of genes involved in myelination and downregulation of genes related to memory and cognition, synaptic transmission, and neuron projection. This novel chimeric model for AD displays human-specific pathological features and allows the analysis of different genetic backgrounds and mutations during the course of the disease.
Keywords: Alzheimer’s disease; cell death; chimeric mouse; dystrophic neurites; expression analysis; human neurons; modeling; neurodegeneration; pluripotent stem cells.
Copyright © 2017 Elsevier Inc. All rights reserved.
Comment in
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Alzheimer disease: A novel human-mouse chimaeric model of Alzheimer disease.Nat Rev Neurol. 2017 Apr;13(4):193. doi: 10.1038/nrneurol.2017.37. Epub 2017 Mar 10. Nat Rev Neurol. 2017. PMID: 28281533 No abstract available.
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Modeling Alzheimer's disease in mice with human neurons.Sci Transl Med. 2017 Mar 15;9(381):eaam9867. doi: 10.1126/scitranslmed.aam9867. Sci Transl Med. 2017. PMID: 28298426
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Neurodegenerative disease: A chimeric approach.Nat Rev Neurosci. 2017 Mar 17;18(4):193. doi: 10.1038/nrn.2017.38. Nat Rev Neurosci. 2017. PMID: 28303018 No abstract available.
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