多巴胺能
黑质
诱导多能干细胞
多巴胺
邻苯二酚-O-甲基转移酶
帕金森病
神经科学
生物
多巴胺转运体
帕金
遗传学
疾病
内科学
医学
基因
胚胎干细胞
基因型
作者
Naoko Kuzumaki,Yukari Suda,Chizuru Iwasawa,Michiko Narita,Michiko Narita,Takefumi Sone,Moe Watanabe,Aya Maekawa,Takuya Matsumoto,Wado Akamatsu,Katsuhide Igarashi,Hideki Tamura,Hideyuki Takeshima,Vivianne L. Tawfik,Toshikazu Ushijima,Nobutaka Hattori,Hideyuki Okano,Minoru Narita,Minoru Narita
出处
期刊:Brain
[Oxford University Press]
日期:2019-03-23
卷期号:142 (6): 1675-1689
被引量:22
摘要
The mechanism by which dopaminergic neurons are selectively affected in Parkinson's disease is not fully understood. In this study, we found a dramatic increase in the expression of catechol-O-methyltransferase (COMT), along with a lower level of DNA methylation, in induced pluripotent stem cell-derived dopaminergic neurons from patients with parkin (PARK2) gene mutations compared to those from healthy controls. In addition, a significant increase in the expression of COMT was found in dopaminergic neurons of isogenic PARK2 induced pluripotent stem cell lines that mimicked loss of function of PARK2 by CRISPR Cas9 technology. In dopamine transporter (DAT)-Cre mice, overexpression of COMT, specifically in dopaminergic neurons of the substantia nigra, produced cataleptic behaviours associated with impaired motor coordination. These findings suggest that upregulation of COMT, likely resulting from DNA hypomethylation, in dopaminergic neurons may contribute to the initial stage of neuronal dysfunction in Parkinson's disease.
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