Human molecular genetics · 2006
Green tea (-)-epigallocatechin-gallate modulates early events in huntingtin misfolding and reduces toxicity in Huntington's disease models.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Ehrnhoefer Dagmar E, Duennwald Martin, Markovic Phoebe, Wacker Jennifer L, Engemann Sabine, Roark Margaret, Legleiter Justin, Marsh J Lawrence, Thompson Leslie M, Lindquist Susan, Muchowski Paul J, Wanker Erich E
Аннотация
Huntington's disease (HD) is a progressive neurodegenerative disorder for which only symptomatic treatments of limited effectiveness are available. Preventing early misfolding steps and thereby aggregation of the polyglutamine (polyQ)-containing protein huntingtin (htt) in neurons of patients may represent an attractive therapeutic strategy to postpone the onset and progression of HD. Here, we demonstrate that the green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) potently inhibits the aggregation of mutant htt exon 1 protein in a dose-dependent manner. Dot-blot assays and atomic force microscopy studies revealed that EGCG modulates misfolding and oligomerization of mutant htt exon 1 protein in vitro, indicating that it interferes with very early events in the aggregation process. Also, EGCG significantly reduced polyQ-mediated htt protein aggregation and cytotoxicity in an yeast model of HD. When EGCG was fed to transgenic HD flies overexpressing a pathogenic htt exon 1 protein, photoreceptor degeneration and motor function improved. These results indicate that modulators of htt exon 1 misfolding and oligomerization like EGCG are likely to reduce polyQ-mediated toxicity in vivo. Our studies may provide the basis for the development of a novel pharmacotherapy for HD and related polyQ disorders.
Предметные рубрики MeSH
AnimalsAnimals, Genetically ModifiedCamellia sinensisCatechinDrosophila melanogasterExonsHumansHuntingtin ProteinHuntington DiseaseIn Vitro TechniquesMicroscopy, Atomic ForceModels, BiologicalMotor NeuronsMultiprotein ComplexesMutationNerve DegenerationNerve Tissue ProteinsNuclear ProteinsPhotoreceptor Cells, InvertebratePhytotherapyProtein ConformationProtein FoldingProtein Structure, QuaternaryRecombinant Fusion ProteinsSaccharomyces cerevisiae