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

被引:346
|
作者
Devine, Michael J. [1 ,2 ]
Ryten, Mina [2 ]
Vodicka, Petr [3 ,4 ]
Thomson, Alison J. [3 ]
Burdon, Tom [3 ]
Houlden, Henry [2 ]
Cavaleri, Fatima [1 ]
Nagano, Masumi [1 ,5 ]
Drummond, Nicola J. [1 ]
Taanman, Jan-Willem [6 ]
Schapira, Anthony H. [6 ]
Gwinn, Katrina [7 ]
Hardy, John [2 ]
Lewis, Patrick A. [2 ]
Kunath, Tilo [1 ]
机构
[1] Univ Edinburgh, MRC Ctr Regenerat Med, Inst Stem Cell Res, Edinburgh EH9 3JQ, Midlothian, Scotland
[2] UCL Inst Neurol, Dept Mol Neurosci, London WC1N 3BG, England
[3] Univ Edinburgh, Roslin Inst, Easter Bush EH25 9RG, Midlothian, Scotland
[4] CAS, Inst Anim Physiol & Genet, Vvi, Libechov 27721, Czech Republic
[5] Univ Tsukuba, Dept Regenerat Med & Stem Cell Biol, Tsukuba, Ibaraki 3058575, Japan
[6] UCL Inst Neurol, Dept Clin Neurosci, London WC1N 3BG, England
[7] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
来源
NATURE COMMUNICATIONS | 2011年 / 2卷
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会;
关键词
GENE DUPLICATION; DEMENTIA; ASSOCIATION; PATIENT; MODELS; BETA; SET; NEURODEGENERATION; PATHOGENESIS; FIBROBLASTS;
D O I
10.1038/ncomms1453
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 alpha-synuclein, causes a fully penetrant, aggressive form of Parkinson's disease with dementia. alpha-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 alpha-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 alpha-synuclein, and to investigate the mechanistic basis of neurodegeneration caused by alpha-synuclein dysfunction.
引用
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页数:10
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