品脱1
帕金
粒体自噬
神经退行性变
细胞生物学
线粒体
生物
运动性
果蝇属(亚属)
神经科学
帕金森病
基因
遗传学
自噬
疾病
内科学
医学
细胞凋亡
作者
Tsuyoshi Inoshita,Kahori Shiba‐Fukushima,Hongrui Meng,Nobutaka Hattori,Yuzuru Imai
摘要
Mitochondrial quality control is a key process in tissues with high energy demands, such as the brain and muscles. Recent studies using Drosophila have revealed that the genes responsible for familial forms of juvenile Parkinson's disease (PD), PINK1 and Parkin regulate mitochondrial function and motility. Cell biological analysis using mammalian cultured cells suggests that the dysregulation of mitophagy by PINK1 and Parkin leads to neurodegeneration in PD. In this chapter, we describe the methods to monitor mitochondrial morphology in the indirect flight muscles of adult Drosophila and Drosophila primary cultured neurons and the methods to analyze the motility of mitochondria in the axonal transport of living larval motor neurons.
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