2 research outputs found
Involvement of casein kinase 1 epsilon/delta (Csnk1e/d) in the pathogenesis of familial Parkinson's disease caused by CHCHD2
Abstract Parkinson's disease (PD) is a common neurodegenerative disorder that results from the loss of dopaminergic neurons. Mutations in coiledâcoilâhelixâcoiledâcoilâhelix domain containing 2 (CHCHD2) gene cause a familial form of PD with αâSynuclein aggregation, and we here identified the pathogenesis of the T61I mutation, the most common diseaseâcausing mutation of CHCHD2. In Neuro2a cells, CHCHD2 is in mitochondria, whereas the T61I mutant (CHCHD2T61I) is mislocalized in the cytosol. CHCHD2T61l then recruits casein kinase 1 epsilon/delta (Csnk1e/d), which phosphorylates neurofilament and αâSynuclein, forming cytosolic aggresomes. In vivo, both Chchd2T61I knockâin and transgenic mice display neurodegenerative phenotypes and aggresomes containing Chchd2T61I, Csnk1e/d, phosphoâαâSynuclein, and phosphoâneurofilament in their dopaminergic neurons. Similar aggresomes were observed in a postmortem PD patient brain and dopaminergic neurons generated from patientâderived iPS cells. Importantly, a Csnk1e/d inhibitor substantially suppressed the phosphorylation of neurofilament and αâSynuclein. The Csnk1e/d inhibitor also suppressed the cellular damage in CHCHD2T61Iâexpressing Neuro2a cells and dopaminergic neurons generated from patientâderived iPS cells and improved the neurodegenerative phenotypes of Chchd2T61I mutant mice. These results indicate that Csnk1e/d is involved in the pathogenesis of PD caused by the CHCHD2T61I mutation