Aggregates from mutant and wild-type α-synuclein proteins and NAC peptide induce apoptotic cell death in human neuroblastoma cells by formation of β-sheet and amyloid-like filaments

被引:328
作者
El-Agnaf, OMA
Jakes, R
Curran, MD
Middleton, D
Ingenito, R
Bianchi, E
Pessi, A
Neill, D
Wallace, A
机构
[1] Queens Univ Belfast, Sch Biol & Biochem, Ctr Peptide & Prot Engn, Belfast BT9 7BL, Antrim, North Ireland
[2] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[3] Belfast City Hosp, No Ireland Histocompatibil & Immunogenet Lab, Belfast BT9 7AB, Antrim, North Ireland
[4] Ist Ric Biol Mol P Angeletti, I-00040 Pomezia, RM, Italy
[5] Newcastle Gen Hosp, Ctr Hlth Elderly, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
基金
英国医学研究理事会;
关键词
alpha-synuclein; Parkinson's disease; Lewy body; toxicity; amyloid; neurodegenerative disease;
D O I
10.1016/S0014-5793(98)01418-5
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
alpha-Synuclein (alpha-syn) protein and a fragment of it, called NAG, have been found in association with the pathological lesions of a number of neurodegenerative diseases, Recently, mutations in the alpha-syn gene have been reported in families susceptible to an inherited form of Parkinson's disease. We have shown that human wild-type alpha-syn, mutant alpha-syn(Ala30Pro) and mutant alpha-syn(Ala53Thr) proteins can self-aggregate and form amyloid-like filaments, Here we report that aggregates of NAC and alpha-syn proteins induced apoptotic cell death in human neuroblastoma SH-SY5Y cells. These findings indicate that accumulation of alpha-syn and its degradation products may play a major role in the development of the pathogenesis of these neurodegenerative diseases. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:71 / 75
页数:5
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