Is there a cause-and-effect relationship between α-synuclein fibrillization and Parkinson's disease?

被引:437
作者
Goldberg, MS
Lansbury, PT
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
关键词
D O I
10.1038/35017124
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The first gene to he linked to Parkinson's disease encodes the neuronal protein alpha-synuclein. Recent mouse and Drosophila models of Parkinson's disease support a central role for the process of alpha-synuclein fibrillization in pathogenesis. However, some evidence indicates that the fibril itself may not be the pathogenic species. Our own biophysical studies suggest that a structured fibrillization intermediate or an alternatively assembled oligomer may be responsible for neuronal death. This speculation can now be experimentally tested in the animal models. Such experiments will have implications for the development of new therapies for Parkinson's disease and related neurodegenerative diseases.
引用
收藏
页码:E115 / E119
页数:5
相关论文
共 48 条
  • [1] Mice lacking α-synuclein display functional deficits in the nigrostriatal dopamine system
    Abeliovich, A
    Schmitz, Y
    Fariñas, I
    Choi-Lundberg, D
    Ho, WH
    Castillo, PE
    Shinsky, N
    Verdugo, JMG
    Armanini, M
    Ryan, A
    Hynes, M
    Phillips, H
    Sulzer, D
    Rosenthal, A
    [J]. NEURON, 2000, 25 (01) : 239 - 252
  • [2] Baba M, 1998, AM J PATHOL, V152, P879
  • [3] Chai YH, 1999, J NEUROSCI, V19, P10338
  • [4] Neurological illness in transgenic mice expressing a prion protein with an insertional mutation
    Chiesa, R
    Piccardo, P
    Ghetti, B
    Harris, DA
    [J]. NEURON, 1998, 21 (06) : 1339 - 1351
  • [5] Fibrils formed in vitro from α-synuclein and two mutant forms linked to Parkinson's disease are typical amyloid
    Conway, KA
    Harper, JD
    Lansbury, PT
    [J]. BIOCHEMISTRY, 2000, 39 (10) : 2552 - 2563
  • [6] Accelerated in vitro fibril formation by a mutant α-synuclein linked to early-onset Parkinson disease
    Conway, KA
    Harper, JD
    Lansbury, PT
    [J]. NATURE MEDICINE, 1998, 4 (11) : 1318 - 1320
  • [7] CONWAY KA, IN PRESS P NATL ACAD
  • [8] Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice
    Cummings, CJ
    Reinstein, E
    Sun, YL
    Antalffy, B
    Jiang, YH
    Ciechanover, A
    Orr, HT
    Beaudet, AL
    Zoghbi, HY
    [J]. NEURON, 1999, 24 (04) : 879 - 892
  • [9] Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1
    Cummings, CJ
    Mancini, MA
    Antalffy, B
    DeFranco, DB
    Orr, HT
    Zoghbi, HY
    [J]. NATURE GENETICS, 1998, 19 (02) : 148 - 154
  • [10] New animal models for Parkinson's disease
    Dawson, TM
    [J]. CELL, 2000, 101 (02) : 115 - 118