Role of Apolipoproteins and α-Synuclein in Parkinson’s Disease

被引:0
作者
Fatemeh Nouri Emamzadeh
机构
[1] University of Lancaster,Division of Biomedical and Life Sciences, Faculty of Health and Medicine
来源
Journal of Molecular Neuroscience | 2017年 / 62卷
关键词
Parkinson’s disease; Apolipoproteins; α-Synuclein;
D O I
暂无
中图分类号
学科分类号
摘要
Parkinson’s disease (PD) is a progressive brain disorder that interferes with activities of normal life. The main pathological feature of this disease is the loss of more than 80% of dopamine-producing neurons in the substantia nigra (SN). Dopaminergic neuronal cell death occurs when intraneuronal, insoluble, aggregated proteins start to form Lewy bodies (LBs), the most important component of which is a protein called α-synuclein (α-syn). α-Syn structurally contains hexameric repeats of 11 amino acids, which are characteristic of apolipoproteins and thus α-syn can also be considered an apolipoprotein. Moreover, apolipoproteins seem to be involved in the incidence and development of PD. Some apolipoproteins such as ApoD have a neuroprotective role in the brain. In PD, apoD levels increase in glial cells surrounding dopaminergic cells. However, elevated levels of some other apolipoproteins such as ApaA1 and ApoE are reported as a vulnerability factor of PD. At present, when a clinical diagnosis of PD is made, based on symptoms such as shaking, stiff muscles and slow movement, serious damage has already been done to nerve cells of the SN. The diagnosis of PD in its earlier stages, before this irreversible damage, would be of enormous benefit for future treatment strategies designed to slow or halt the progression of PD. This review presents the roles of apolipoproteins and α-syn in PD and how some of them could potentially be used as biomarkers for PD.
引用
收藏
页码:344 / 355
页数:11
相关论文
共 758 条
[1]  
Acciarri A(2006)ApoE epsilon2-epsilon4 genotype is a possible risk factor for primary progressive aphasia Ann Neurol 59 436-437
[2]  
Masullo C(2009)Apolipoprotein E epsilon4 is associated with disease-specific effects on brain atrophy in Alzheimer’s disease and frontotemporal dementia Proc Natl Acad Sci USA 106 2018-2022
[3]  
Bizzarro A(2015)Heart rate variability and the risk of Parkinson disease: the atherosclerosis risk in communities study Ann Neurol 77 877-883
[4]  
Agosta F(2011)Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission Neurobiol Dis 42 360-367
[5]  
Vossel KA(2000)Wild-type but not Parkinson’s disease-related ala-53 → Thr mutant α-synuclein protects neuronal cells from apoptotic stimuli Biol Chem 275 24065-24069
[6]  
Miller BL(2010)Brain lipid metabolism, apolipoprotein E and the pathophysiology of Alzheimer’s disease Neuropharmacology 59 295-302
[7]  
Migliaccio R(2015)Prion-like propagation of human brain-derived alpha-synuclein in transgenic mice expressing human wild-type alpha-synuclein Acta Neuropathol Commun 3 75-239
[8]  
Bonasera SJ(2010)Alpha-synuclein overexpression increases dopamine toxicity in BE2-M17 cells BMC Neurosci 11 41-211
[9]  
Filippi M(2006)Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson’s disease Neurosci Lett 406 235-632
[10]  
Boxer AL(2003)Staging of brain pathology related to sporadic Parkinson’s disease Neurobiol Aging 24 197-316