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• W2614932012 abstract "Abstract Parkinson′s disease is a progressive age-associated neurological disorder. One of the major neuropathological hallmarks of Parkinson’s disease is the appearance of protein aggregates, mainly consisting of the protein alpha-Synuclein. These aggregates have been described both in genetic as well as idiopathic forms of the disease. Currently, Parkinson’s disease patient-specific induced pluripotent stem cells (iPSCs) are mainly used for in vitro disease modeling or for experimental cell replacement approaches. Here, we demonstrate that these cells can be used for in vivo disease modeling. We show that Parkinson’s disease patient-specific, iPSC-derived neurons carrying the LRRK2-G2019S mutation show an upregulation of alpha-Synuclein after transplantation in the mouse brain. However, further investigations indicate that the increased human alpha-Synuclein levels fail to induce spreading or aggregation in the mouse brain. We therefore conclude that grafting of these cells into the mouse brain is suitable for cell autonomous in vivo disease modeling but has strong limitations beyond that. Furthermore, our results support the hypothesis that there might be a species barrier between human to mouse concerning alpha-Synuclein spreading." @default.
• W2614932012 created "2017-05-26" @default.
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• W2614932012 date "2017-05-19" @default.
• W2614932012 modified "2023-09-26" @default.
• W2614932012 title "In vivo phenotyping of Parkinson-specific stem cells reveals increased a-Synuclein levels but no spreading" @default.
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• W2614932012 doi "https://doi.org/10.1101/140178" @default.
• W2614932012 hasPublicationYear "2017" @default.
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