| Literature DB >> 31135049 |
Naoko Kuzumaki1,2, Yukari Suda1, Chizuru Iwasawa1, Michiko Narita1, Takefumi Sone2, Moe Watanabe1, Aya Maekawa3, Takuya Matsumoto2, Wado Akamatsu2,4, Katsuhide Igarashi1, Hideki Tamura1, Hideyuki Takeshima5, Vivianne L Tawfik6, Toshikazu Ushijima1,5, Nobutaka Hattori7, Hideyuki Okano1,2, Minoru Narita1.
Abstract
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.Entities:
Keywords: zzm321990 COMTzzm321990 ; Parkinson’s disease; dopaminergic neuron; epigenetic modification; iPS
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Year: 2019 PMID: 31135049 DOI: 10.1093/brain/awz084
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501