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Review
. 2020 Apr 1;1866(4):165431.
doi: 10.1016/j.bbadis.2019.03.004. Epub 2019 Mar 18.

Using induced pluripotent stem cell neuronal models to study neurodegenerative diseases

Affiliations
Review

Using induced pluripotent stem cell neuronal models to study neurodegenerative diseases

Xinwen Zhang et al. Biochim Biophys Acta Mol Basis Dis. .

Abstract

Current application of human induced pluripotent stem cells (hiPSCs) technology in patient-specific models of neurodegenerative disorders recapitulate some of key phenotypes of diseases, representing disease-specific cellular modeling and providing a unique platform for therapeutics development. We review recent efforts toward advancing hiPSCs-derived neuronal cell types and highlight their potential use for the development of more complex in vitro models of neurodegenerative diseases by focusing on Alzheimer's disease, Parkinson's disease, Huntington's disease and Amyotrophic lateral sclerosis. We present evidence from previous works on the important phenotypic changes of various neuronal types in these neurological diseases. We also summarize efforts on conducting low- and high-throughput screening experiments with hiPSCs toward developing potential therapeutics for treatment of neurodegenerative diseases. Lastly, we discuss the limitations of hiPSCs culture system in studying neurodegenerative diseases and alternative strategies to overcome these hurdles.

Keywords: Disease modeling; Induced pluripotent stem cells; Neurodegeneration; Neurodegenerative disease; Neurons; Therapeutic development.

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Conflict of interest statement

Conflict of Interests

The authors claim no conflict of interest

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References

    1. Takahashi K, Yamanaka S, Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors, Cell, 126 (2006) 663–676. - PubMed
    1. Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K, Yamanaka S, Induction of pluripotent stem cells from adult human fibroblasts by defined factors, Cell, 131 (2007) 861–872. - PubMed
    1. Izpisua Belmonte JC, Ellis J, Hochedlinger K, Yamanaka S, Induced pluripotent stem cells and reprogramming: seeing the science through the hype, Nat Rev Genet, 10 (2009) 878–883. - PubMed
    1. Robinton DA, Daley GQ, The promise of induced pluripotent stem cells in research and therapy, Nature, 481 (2012) 295–305. - PMC - PubMed
    1. Shi Y, Inoue H, Wu JC, Yamanaka S, Induced pluripotent stem cell technology: a decade of progress, Nat Rev Drug Discov, 16 (2017) 115–130. - PMC - PubMed

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