Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782222078452170752 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3265381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT devinemichaelj parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT rytenmina parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT vodickapetr parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT thomsonalisonj parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT burdontom parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT houldenhenry parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT cavalerifatima parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT naganomasumi parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT drummondnicolaj parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT taanmanjanwillem parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT schapiraanthonyh parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT gwinnkatrina parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT hardyjohn parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT lewispatricka parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus AT kunathtilo parkinsonsdiseaseinducedpluripotentstemcellswithtriplicationoftheasynucleinlocus |