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橄榄苦苷配基:一种具有不同靶标对抗淀粉样毒性的多酚。

Oleuropein aglycone: A polyphenol with different targets against amyloid toxicity.

机构信息

Department of Biomedical, Experimental and Clinical Sciences 'Mario Serio', University of Florence, Viale Morgagni, 50 50134 Florence, Italy; Department of Neuroscience, Psychology, Area of Medicine and Health of the Child of the University of Florence, Viale Pieraccini, 6, 50139 Florence, Italy.

Department of Physics, University of Genova, via Dodecaneso 33, 16146, Genova, Italy.

出版信息

Biochim Biophys Acta Gen Subj. 2018 Jun;1862(6):1432-1442. doi: 10.1016/j.bbagen.2018.03.023. Epub 2018 Mar 21.

Abstract

BACKGROUND

Many data highlight the benefits of the Mediterranean diet and its main lipid component, extra-virgin olive oil (EVOO). EVOO contains many phenolic compounds that have been found effective against several aging- and lifestyle-related diseases, including neurodegeneration. Oleuropein, a phenolic secoiroid glycoside, is the main polyphenol in the olive oil. It has been reported that the aglycone form of Oleuropein (OleA) interferes in vitro and in vivo with amyloid aggregation of a number of proteins/peptides involved in amyloid, particularly neurodegenerative, diseases avoiding the growth of toxic oligomers and displaying protection against cognitive deterioration.

METHODS

In this study, we carried out a cellular and biophysical study on the relationships between the effects of OleA on the aggregation and cell interactions of the D76N β2-microglobulin (D76N b2m) variant associated with a familial form of systemic amyloidosis with progressive bowel dysfunction and extensive visceral amyloid deposits.

RESULTS

Our results indicate that OleA protection against D76N b2m cytotoxicity results from i) a modification of the conformational and biophysical properties of its amyloid fibrils; ii) a modification of the cell bilayer surface properties of exposed cells.

CONCLUSIONS

This study reveals that OleA remodels not only D76N b2m aggregates but also the cell membrane interfering with the misfolded proteins-cell membrane association, in most cases an early event triggering amyloid-mediated cytotoxicity.

GENERAL SIGNIFICANCE

The data provided in the present article focus on OleA protection, featuring this polyphenol as a promising plant molecule useful against amyloid diseases.

摘要

背景

许多数据强调了地中海饮食及其主要脂质成分特级初榨橄榄油(EVOO)的益处。EVOO 含有许多酚类化合物,这些化合物已被证明对多种与衰老和生活方式相关的疾病有效,包括神经退行性疾病。橄榄苦苷,一种酚类倍半萜糖苷,是橄榄油中的主要多酚。据报道,橄榄苦苷的糖苷配基形式(OleA)在体外和体内干扰几种与淀粉样蛋白相关的蛋白质/肽的淀粉样聚集,特别是神经退行性疾病,避免了毒性寡聚物的生长,并显示出对认知恶化的保护作用。

方法

在这项研究中,我们对 OleA 对与家族性系统性淀粉样变性相关的 D76N β2-微球蛋白(D76N b2m)变体的聚集和细胞相互作用的影响之间的关系进行了细胞和生物物理研究,该变体与进行性肠功能障碍和广泛内脏淀粉样沉积有关。

结果

我们的结果表明,OleA 对 D76N b2m 细胞毒性的保护作用来自于:i)其淀粉样纤维的构象和生物物理性质的改变;ii)暴露细胞的细胞膜表面性质的改变。

结论

这项研究表明,OleA 不仅重塑了 D76N b2m 聚集物,而且还重塑了细胞膜,干扰了错误折叠蛋白与细胞膜的结合,在大多数情况下,这是触发淀粉样蛋白介导的细胞毒性的早期事件。

一般意义

本文提供的数据集中在 OleA 的保护作用上,突出了这种多酚作为一种有前途的植物分子,可用于对抗淀粉样疾病。

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