α-synuclein protects SH-SY5Y cells from dopamine toxicity

被引:34
作者
Colapinto, Monica
Mila, Silvia
Giraudo, Sabrina
Stefanazzi, Paola
Molteni, Monica
Rossetti, Carlo
Bergamasco, Bruno
Lopiano, Leonardo
Fasano, Mauro
机构
[1] Univ Insubria, Dept Struct & Funct Biol, I-21052 Busto Arsizio, VA, Italy
[2] Univ Insubria, Ctr Neurosci, I-21052 Busto Arsizio, VA, Italy
[3] Univ Turin, Dept Neurosci, I-10126 Turin, Italy
[4] Univ Insubria, Dept Biotechnol & Mol Sci, I-21100 Varese, Italy
[5] IRCCS, Salvatore Maugeri Fdn, I-27100 Pavia, Italy
关键词
14-3-3; protein; alpha-synuclein; DJ-1; dopamine toxicity; HSP70; human neuroblastoma; oxidative stress; Parkinson's disease; two-dimensional electrophoresis;
D O I
10.1016/j.bbrc.2006.08.163
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dopaminergic human neuroblastoma SH-SY5Y cells were stably transformed to increase expression of alpha-synuclein, a Parkinson's disease-related protein. Transformed cells were more resistant to oxidative insults, showing a cytoprotective role of alpha-synuclein. The expression of redox chaperonins (DJ-1, HSP70, and 14-3-3) was evaluated by Western blotting. Expression of alpha-synuclein reduced HSP70 levels even in the presence of dopamine, with a twofold increase of DJ-1 in the absence of oxidants. DJ-1 is significantly reduced by dopamine, and even more by dopamine and Cu(II). Increased alpha-synuclein expression did not affect 14-3-3, although dopamine increased its level by 60% in wild-type cells. alpha-Synuclein not only upregulated DJ-1, but also shifted all DJ-1 forms to a single spot at pI = 5.7 not observed in wild-type cells. Dopamine gradually restored the distribution of DJ-I forms to a situation similar to wildtype cells, with the form at pI = 6.1 progressively enriched under oxidative conditions. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1294 / 1300
页数:7
相关论文
共 60 条
[1]   Protective effect of TAT-delivered α-synuclein:: relevance of the C-terminal domain and involvement of HSP70 [J].
Albani, D ;
Peverelli, E ;
Rametta, R ;
Batelli, S ;
Veschini, L ;
Negro, A ;
Forloni, G .
FASEB JOURNAL, 2004, 18 (12) :1713-+
[2]   Neurodegenerative diseases and oxidative stress [J].
Barnham, KJ ;
Masters, CL ;
Bush, AI .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (03) :205-214
[3]   A topological model of the interaction between α-synuclein and sodium dodecyl sulfate micelles [J].
Bisaglia, M ;
Tessari, I ;
Pinato, L ;
Bellanda, M ;
Giraudo, S ;
Fasano, M ;
Bergantino, E ;
Bubacco, L ;
Mammi, S .
BIOCHEMISTRY, 2005, 44 (01) :329-339
[4]   Functional changes of the basal ganglia circuitry in Parkinson's disease [J].
Blandini, F ;
Nappi, G ;
Tassorelli, C ;
Martignoni, E .
PROGRESS IN NEUROBIOLOGY, 2000, 62 (01) :63-88
[5]   Extracellular toxicity of 6-hydroxydopamine on PC12 cells [J].
Blum, D ;
Torch, S ;
Nissou, MF ;
Benabid, AL ;
Verna, JM .
NEUROSCIENCE LETTERS, 2000, 283 (03) :193-196
[6]   Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism [J].
Bonifati, V ;
Rizzu, P ;
van Baren, MJ ;
Schaap, O ;
Breedveld, GJ ;
Krieger, E ;
Dekker, MCJ ;
Squitieri, F ;
Ibanez, P ;
Joosse, M ;
van Dongen, JW ;
Vanacore, N ;
van Swieten, JC ;
Brice, A ;
Meco, G ;
van Duijn, CM ;
Oostra, BA ;
Heutink, P .
SCIENCE, 2003, 299 (5604) :256-259
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]   A structural and functional role for 11-mer repeats in α-synuclein and other exchangeable lipid binding proteins [J].
Bussell, R ;
Eliezer, D .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 329 (04) :763-778
[9]  
Cabin DE, 2002, J NEUROSCI, V22, P8797
[10]   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