Analysis of autophagic impairment in neurons derived from familial parkinson's disease
Project/Area Number |
26893263
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Neurology
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Research Institution | Juntendo University |
Principal Investigator |
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Project Period (FY) |
2014-08-29 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
|
Keywords | パーキンソン病 / iPS細胞 / オートファジー |
Outline of Final Research Achievements |
PARK9-iPS cells were established from the patient's T-cell. We established a highly efficient induction method from the iPS cells into dopaminergic neurons. We found lysosomal abnormalities and impairment of autophagy in PARK9-dopaminergic neurons derived from iPS cells using the new induction method. We established mutation-corrected PARK9-iPS cell line using CRISPR/CAS9 system. We also detect abnormalities of mitopahagy in PARK2-dopaminergic neurons.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Ethambutol neutralizes lysosomes and causes lysosomal zinc accumulation.2015
Author(s)
Yamada D, Saiki S, Furuya N, Ishikawa K, Imamichi Y, Kambe T, Fujimura T, Ueno T, Koike M, Sumiyoshi K, Hattori N
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Journal Title
Biochem Biophys Res Commun.
Volume: 471
Issue: 1
Pages: 109-116
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Presentation] 抗結核薬エタンブトールのオートファジー阻害作用2014
Author(s)
山田大介, 斉木臣二, 古屋徳彦, 石川景一, 今道洋子, 神戸大朋, 藤村 務, 上野隆, 小池正人, 服部信孝
Organizer
第8回オートファジー研究会・第2回新学術「オートファジー」班会議
Place of Presentation
シャトレーゼ ガトーキングダムサッポロ
Year and Date
2014-11-10 – 2014-11-11
Related Report