کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
8326277 1539965 2008 16 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Potential pathogenic role of β-amyloid1-42-aluminum complex in Alzheimer's disease
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Potential pathogenic role of β-amyloid1-42-aluminum complex in Alzheimer's disease
چکیده انگلیسی
The etiopathogenesis of Alzheimer's disease is far from being clearly understood. However, the involvement of metal ions as a potential key factor towards conformational modifications and aggregation of amyloid is widely recognized. The aim of the present study is to shed some light on the relationship between metal ions, amyloid conformation/aggregation, and their potential relationship with the conformational aspects of AD. We compare the effects of β-amyloid1-42 and its various metal complexes (β-amyloid-Al, β-amyloid-Zn, β-amyloid-Cu, β-amyloid-Fe) in human neuroblastoma cells in terms of cell viability, membrane structure properties, and cell morphology. No significant toxic effects were observed in neuroblastoma cells after 24 h treatment both with β-amyloid and β-amyloid-metals (β-amyloid-Zn, β-amyloid-Cu, β-amyloid-Fe); on the other hand, there was a marked reduction of cellular viability after treatment with β-amyloid-Al complex. In addition, treatment with β-amyloid-Al increased membrane fluidity much more than other β-amyloid-metal complexes, whose contribution was negligible. Furthermore, the cellular morphology, as observed by electron microscopy, was deeply altered by β-amyloid-Al. Importantly, β-amyloid-Al toxicity is closely and significantly associated with a great difference in the structure/aggregation of this complex with respect to that of β-amyloid alone and other β-amyloid-metal complexes. In addition, β-amyloid, as a consequence of Al binding, becomes strongly hydrophobic in character. These findings show a significant involvement of Al, compared to the other metal ions used in our experiments, in promoting a specific amyloid1-42 aggregation, which is able to produce marked toxic effects on neuroblastoma cells, as clearly demonstrated for the first time in this study.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The International Journal of Biochemistry & Cell Biology - Volume 40, Issue 4, 2008, Pages 731-746
نویسندگان
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