Oxidative stress and cellular pathologies in Parkinson’s disease

被引:0
作者
Lesly Puspita
Sun Young Chung
Jae-won Shim
机构
[1] Soonchunhyang Institute of Medi-bio Science (SIMS),Center for Stem Cell Biology
[2] Soonchunhyang University,undefined
[3] Sloan-Kettering Institute,undefined
来源
Molecular Brain | / 10卷
关键词
Alpha-synuclein; Dopamine neurons; Mitochondria; Oxidative stress; Parkinson’s disease; Reactive oxygen species; Unfolded protein response;
D O I
暂无
中图分类号
学科分类号
摘要
Parkinson’s disease (PD) is a chronic and progressive neurodegeneration of dopamine neurons in the substantia nigra. The reason for the death of these neurons is unclear; however, studies have demonstrated the potential involvement of mitochondria, endoplasmic reticulum, α-synuclein or dopamine levels in contributing to cellular oxidative stress as well as PD symptoms. Even though those papers had separately described the individual roles of each element leading to neurodegeneration, recent publications suggest that neurodegeneration is the product of various cellular interactions. This review discusses the role of oxidative stress in mediating separate pathological events that together, ultimately result in cell death in PD. Understanding the multi-faceted relationships between these events, with oxidative stress as a common denominator underlying these processes, is needed for developing better therapeutic strategies.
引用
收藏
相关论文
共 592 条
[1]  
Bellucci A(2016)Review: Parkinson’s disease: from synaptic loss to connectome dysfunction Neuropathol Appl Neurobiol 42 77-94
[2]  
Mercuri NB(2012)Low nigrostriatal reserve for motor parkinsonism in nonhuman primates Exp Neurol 237 355-362
[3]  
Venneri A(2004)Hereditary early-onset Parkinson’s disease caused by mutations in PINK1 Science 304 1158-1160
[4]  
Faustini G(1997)Mutation in the alpha-synuclein gene identified in families with Parkinson’s disease Science 276 2045-2047
[5]  
Longhena F(2005)A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson’s disease Lancet 365 412-415
[6]  
Pizzi M(2005)Genetic screening for a single common LRRK2 mutation in familial Parkinson’s disease Lancet 365 410-412
[7]  
Tabbal SD(2003)Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism Science 299 256-259
[8]  
Tian LL(1997)Alpha-synuclein in Lewy bodies Nature 388 839-840
[9]  
Karimi M(2012)From α-synuclein to synaptic dysfunctions: new insights into the pathophysiology of Parkinson’s disease Brain Res 1476 183-202
[10]  
Brown CA(2015)The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy Nature 524 309-314