Insights into the molecular basis of the differing susceptibility of varying cell types to the toxicity of amyloid aggregates

被引:79
作者
Cecchi, C
Baglioni, S
Fiorillo, C
Pensalfini, A
Liguri, G
Nosi, D
Rigacci, S
Bucciantini, M
Stefani, M [1 ]
机构
[1] Univ Florence, Dept Biochem Sci, I-50134 Florence, Italy
[2] Univ Florence, Dept Anat Histol & Forens Med, I-50134 Florence, Italy
[3] Univ Florence, Ctr Excellence Mol & Clin Studies Chron Inflammat, I-50134 Florence, Italy
[4] Univ Florence, Interuniv Ctr Study Mol Basis Neurodegenerat Dis, I-50134 Florence, Italy
关键词
amyloid toxicity; pre-fibrillar protein aggregates; conformational diseases; folding and disease; protein misfolding and citotoxicity;
D O I
10.1242/jcs.02473
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It has been reported that different tissue or cultured cell types are variously affected by the exposure to toxic protein aggregates, however a substantial lack of information exists about the biochemical basis of cell resistance or susceptibility to the aggregates. We investigated the extent of the cytotoxic effects elicited by supplementing the media of a panel of cultured cell lines with aggregates of HypF-N, a prokaryotic domain not associated with any amyloid disease. The cell types exposed to early, pre-fibrillar aggregates (not mature fibrils) displayed variable susceptibility to damage and to apoptotic death with a significant inverse relation to membrane content in cholesterol. Susceptibility to damage by the aggregates was also found to be significantly related to the ability of cells to counteract early modifications of the intracellular free Ca2+ and redox status. Accordingly, cell resistance appeared related to the efficiency of the biochemical equipment leading any cell line to sustain the activity of Ca2+ pumps while maintaining under control the oxidative stress associated with the increased metabolic rate. Our data depict membrane destabilization and the subsequent early derangement of ion balance and intracellular redox status as key events in targeting exposed cells to apoptotic death.
引用
收藏
页码:3459 / 3470
页数:12
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