神经退行性变
粒体自噬
神经保护
解偶联蛋白
线粒体
生物
细胞生物学
秀丽隐杆线虫
突变体
神经科学
生物化学
内科学
基因
医学
细胞凋亡
自噬
褐色脂肪组织
疾病
脂肪组织
作者
In‐Jeong Cho,Hyun‐Ok Song,Jeong Hoon Cho
出处
期刊:PubMed
日期:2017-11-30
卷期号:40 (11): 864-870
被引量:17
标识
DOI:10.14348/molcells.2017.0172
摘要
The uncoupling protein 4 (ucp-4) gene is involved in age-dependent neurodegeneration in C. elegans. Therefore, we aimed to investigate the mechanism underlying the association between mitochondrial uncoupling and neurodegeneration by examining the effects of uncoupling agents and ucp-4 overexpression in C. elegans. Treatment with either DNP or CCCP improved neuronal defects in wild type during aging. Uncoupling agents also restored neuronal phenotypes of ucp-4 mutants to those exhibited by wild type, while ucp-4 overexpression attenuated the severity of age-dependent neurodegeneration. Neuronal improvements were further associated with reductions in mitochondrial membrane potentials. However, these age-dependent neuroprotective effects were limited in mitophagy-deficient mutant, pink-1, background. These results suggest that membrane uncoupling can attenuate age-dependent neurodegeneration by stimulating mitophagy.
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