Generation of induced pluripotent stem cells from a young-onset Parkinson's disease patient carrying the compound heterozygous PLA2G6 p.D331Y/p.M358IfsX mutations

被引:3
|
作者
Chiu, Ching-Chi [1 ,2 ,3 ]
Wang, Hung-Li [1 ,4 ,5 ]
Weng, Yi-Hsin [6 ,7 ]
Chen, Rou-Shayn [6 ,7 ]
Chen, Chiung-Mei [6 ,7 ]
Yeh, Tu-Hsueh [1 ,8 ]
Lu, Chin-Song [1 ,7 ]
Chen, Yu-Jie [1 ]
Liu, Yu-Chuan [9 ]
Huang, Ying-Zu [1 ,5 ,7 ,10 ]
Chang, Kuo-Hsuan [6 ,7 ]
机构
[1] Chang Gung Mem Hosp Linkou, Neurosci Res Ctr, Taoyuan, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Med Biotechnol & Lab Sci, Taoyuan, Taiwan
[3] Chang Gung Univ Sci & Technol, Dept Nursing, Taoyuan, Taiwan
[4] Chang Gung Univ, Dept Physiol & Pharmacol, Coll Med, Taoyuan, Taiwan
[5] Chang Gung Univ, Coll Med, Hlth Aging Res Ctr, Taoyuan, Taiwan
[6] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[7] Chang Gung Mem Hosp Linkou, Dept Neurol, Taoyuan, Taiwan
[8] Taipei Med Univ Hosp, Dept Neurol, Taipei, Taiwan
[9] Taiwan Landseed Hosp, Div Sports Med, Taoyuan, Taiwan
[10] Natl Cent Univ, Inst Cognit Neurosci, Taoyuan, Taiwan
关键词
D O I
10.1016/j.scr.2019.101552
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mutations in PLA2G6 gene cause PLA2G6-associated neurodegeneration, including recessive familial type 14 of Parkinson's disease (PARK14). Previously, we identified PARK14 patients with compound heterozygous c.991G > T/c.1077G > A (p.D331Y/p.M358IfsX) mutations. The c.1077G > A mutation led to a four base-pairs deletion and frameshift mutation (p.M358IfsX) of PLA2G6 mRNA. We established induced pluripotent stem cells (iPSCs) from peripheral blood mononuclear cells of a female patient with compound heterozygous c.991G > T/c.1077G > A (p.D331Y/ p.M358IfsX) mutations by using Sendai-virus delivery system. The iPSCs exhibited pluripotency and in vivo differentiation potential. The iPSCs can be used for studying the molecular pathogenic mechanism of PARK14.
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页数:5
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