Mechanisms of Parkinson's disease linked to pathological α-synuclein:: New targets for drug discovery

被引:379
作者
Lee, Virginia M. -Y. [1 ]
Trojanowski, John Q. [1 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Ctr Neurodegenerat Dis Res, Inst Aging, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/j.neuron.2006.09.026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Classic Parkinson's disease (PD) is characterized by fibrillar alpha-synuclein inclusions known as Lewy bodies in the substantia nigra, which are associated with nigrostriatal degeneration. However, alpha-synuclein pathologies accumulate throughout the CNS in areas that also undergo progressive neurodegeneration, leading to dementia and other behavioral impairments in addition to parkinsonism. Although mutations in the alpha-synuclein gene only cause Lewy body PD in rare families, and although there are multiple other, albeit rare, genetic causes of familial parkinsonism, sporadic Lewy body PD is the most common movement disorder, and insights into mechanisms underlying alpha-synuclein-mediated neurodegeneration provide novel targets for the discovery of disease-modifying therapies for PD and related neurodegenerative alpha-synucleinopathies.
引用
收藏
页码:33 / 38
页数:6
相关论文
共 31 条
[1]  
Abdi F, 2006, J ALZHEIMERS DIS, V9, P293
[2]  
Alzheimers Assoc, 1998, NEUROBIOL AGING, V19, P109
[3]   Drosophila as a model for human neurodegenerative disease [J].
Bilen, J ;
Bonini, NM .
ANNUAL REVIEW OF GENETICS, 2005, 39 :153-171
[4]   α-synuclein cooperates with CSPα in preventing neurodegeneration [J].
Chandra, S ;
Gallardo, G ;
Fernández-Chacón, R ;
Schlüter, OM ;
Südhof, TC .
CELL, 2005, 123 (03) :383-396
[5]   α-synuclein locus duplication as a cause of familial Parkinson's disease [J].
Chartier-Harlin, MC ;
Kachergus, J ;
Roumier, C ;
Mouroux, V ;
Douay, X ;
Lincoln, S ;
Levecque, C ;
Larvor, L ;
Andrieux, J ;
Hulihan, M ;
Waucquier, N ;
Defebvre, L ;
Amouyel, P ;
Farrer, M ;
Destée, A .
LANCET, 2004, 364 (9440) :1167-1169
[6]   Kinetic stabilization of the α-synuclein protofibril by a dopamine-α-synuclein adduct [J].
Conway, KA ;
Rochet, JC ;
Bieganski, RM ;
Lansbury, PT .
SCIENCE, 2001, 294 (5545) :1346-1349
[7]   The biochemistry of Parkinson's disease [J].
Cookson, MR .
ANNUAL REVIEW OF BIOCHEMISTRY, 2005, 74 :29-52
[8]   α-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models [J].
Cooper, Antony A. ;
Gitler, Aaron D. ;
Cashikar, Anil ;
Haynes, Cole M. ;
Hill, Kathryn J. ;
Bhullar, Bhupinder ;
Liu, Kangning ;
Xu, Kexiang ;
Strathearn, Katherine E. ;
Liu, Fang ;
Cao, Songsong ;
Caldwell, Kim A. ;
Caldwell, Guy A. ;
Marsischky, Gerald ;
Kolodner, Richard D. ;
LaBaer, Joshua ;
Rochet, Jean-Christophe ;
Bonini, Nancy M. ;
Lindquist, Susan .
SCIENCE, 2006, 313 (5785) :324-328
[9]   Impaired degradation of mutant α-synuclein by chaperone-mediated autophagy [J].
Cuervo, AM ;
Stefanis, L ;
Fredenburg, R ;
Lansbury, PT ;
Sulzer, D .
SCIENCE, 2004, 305 (5688) :1292-1295
[10]  
FAN Y, 2006, IN PRESS HUM MOL GEN