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Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus

A major barrier to research on Parkinson's disease is inaccessibility of diseased tissue for study. One solution is to derive induced pluripotent stem cells from patients and differentiate them into neurons affected by disease. Triplication of SNCA, encoding α-synuclein, causes a fully penetran...

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Autores principales: Devine, Michael J., Ryten, Mina, Vodicka, Petr, Thomson, Alison J., Burdon, Tom, Houlden, Henry, Cavaleri, Fatima, Nagano, Masumi, Drummond, Nicola J., Taanman, Jan-Willem, Schapira, Anthony H., Gwinn, Katrina, Hardy, John, Lewis, Patrick A., Kunath, Tilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265381/
https://www.ncbi.nlm.nih.gov/pubmed/21863007
http://dx.doi.org/10.1038/ncomms1453
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author Devine, Michael J.
Ryten, Mina
Vodicka, Petr
Thomson, Alison J.
Burdon, Tom
Houlden, Henry
Cavaleri, Fatima
Nagano, Masumi
Drummond, Nicola J.
Taanman, Jan-Willem
Schapira, Anthony H.
Gwinn, Katrina
Hardy, John
Lewis, Patrick A.
Kunath, Tilo
author_facet Devine, Michael J.
Ryten, Mina
Vodicka, Petr
Thomson, Alison J.
Burdon, Tom
Houlden, Henry
Cavaleri, Fatima
Nagano, Masumi
Drummond, Nicola J.
Taanman, Jan-Willem
Schapira, Anthony H.
Gwinn, Katrina
Hardy, John
Lewis, Patrick A.
Kunath, Tilo
author_sort Devine, Michael J.
collection PubMed
description A major barrier to research on Parkinson's disease is inaccessibility of diseased tissue for study. One solution is to derive induced pluripotent stem cells from patients and differentiate them into neurons affected by disease. Triplication of SNCA, encoding α-synuclein, causes a fully penetrant, aggressive form of Parkinson's disease with dementia. α-Synuclein dysfunction is the critical pathogenic event in Parkinson's disease, multiple system atrophy and dementia with Lewy bodies. Here we produce multiple induced pluripotent stem cell lines from an SNCA triplication patient and an unaffected first-degree relative. When these cells are differentiated into midbrain dopaminergic neurons, those from the patient produce double the amount of α-synuclein protein as neurons from the unaffected relative, precisely recapitulating the cause of Parkinson's disease in these individuals. This model represents a new experimental system to identify compounds that reduce levels of α-synuclein, and to investigate the mechanistic basis of neurodegeneration caused by α-synuclein dysfunction.
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spelling pubmed-32653812012-01-24 Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus Devine, Michael J. Ryten, Mina Vodicka, Petr Thomson, Alison J. Burdon, Tom Houlden, Henry Cavaleri, Fatima Nagano, Masumi Drummond, Nicola J. Taanman, Jan-Willem Schapira, Anthony H. Gwinn, Katrina Hardy, John Lewis, Patrick A. Kunath, Tilo Nat Commun Article A major barrier to research on Parkinson's disease is inaccessibility of diseased tissue for study. One solution is to derive induced pluripotent stem cells from patients and differentiate them into neurons affected by disease. Triplication of SNCA, encoding α-synuclein, causes a fully penetrant, aggressive form of Parkinson's disease with dementia. α-Synuclein dysfunction is the critical pathogenic event in Parkinson's disease, multiple system atrophy and dementia with Lewy bodies. Here we produce multiple induced pluripotent stem cell lines from an SNCA triplication patient and an unaffected first-degree relative. When these cells are differentiated into midbrain dopaminergic neurons, those from the patient produce double the amount of α-synuclein protein as neurons from the unaffected relative, precisely recapitulating the cause of Parkinson's disease in these individuals. This model represents a new experimental system to identify compounds that reduce levels of α-synuclein, and to investigate the mechanistic basis of neurodegeneration caused by α-synuclein dysfunction. Nature Pub. Group 2011-08-23 /pmc/articles/PMC3265381/ /pubmed/21863007 http://dx.doi.org/10.1038/ncomms1453 Text en Copyright © 2011, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Devine, Michael J.
Ryten, Mina
Vodicka, Petr
Thomson, Alison J.
Burdon, Tom
Houlden, Henry
Cavaleri, Fatima
Nagano, Masumi
Drummond, Nicola J.
Taanman, Jan-Willem
Schapira, Anthony H.
Gwinn, Katrina
Hardy, John
Lewis, Patrick A.
Kunath, Tilo
Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
title Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
title_full Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
title_fullStr Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
title_full_unstemmed Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
title_short Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
title_sort parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265381/
https://www.ncbi.nlm.nih.gov/pubmed/21863007
http://dx.doi.org/10.1038/ncomms1453
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