阿尔茨海默病:分子标记和酵母模型

T. N. Goleva, A. Rogov, R. Zvyagilskaya
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引用次数: 5

摘要

阿尔茨海默病是一种多方面的、无法治愈的神经系统疾病,其特征是认知能力下降和大脑神经元退化。与阿尔茨海默病有关的主要因素包括错误折叠和聚集蛋白的积累(微管相关蛋白过度磷酸化,称为tau和淀粉样蛋白Aβ)、氧化损伤、炎症、线粒体损伤和慢性能量失衡、慢性内质网应激、自噬功能障碍、线粒体相关的内质网膜的异常和功能障碍,作为内质网和线粒体之间的桥梁,调节多种功能,如Ca2+转移,能量交换,脂质合成和运输和蛋白质折叠,溶酶体基因的遗传变异,代谢组学的变化很快被考虑。在转基因Aβ动物模型中,我们特别强调了线粒体裂变(断裂)是阿尔茨海默病病理之前的一个重要早期事件,以及细胞外淀粉样蛋白沉积的显著减少,预防认知缺陷的发展和抑制线粒体动力学异常后突触参数的改善。在揭示阿尔茨海默病复杂的基本细胞内机制方面,具有良好特征的酿酒酵母作为一种有价值的真核模式生物的重要作用得到了强调。应用一种新的模式生物酵母解脂耶氏菌的好处是,它是一种专性需氧菌,呼吸代谢与哺乳动物细胞非常相似,适合经典和分子遗传技术,作为异源蛋白的生产者有着悠久的历史,具有改变其形态(从酵母样到真正的菌丝体)以响应环境条件的能力,作为一种有用的替代方案,在阿尔茨海默病酵母模型中解释线粒体动力学和分布的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alzheimer’s Disease: Molecular Hallmarks and Yeast Models
Alzheimer’s disease is a multifaceted, incurable neurologic disorder characterized by cognitive decline and degeneration of brain neurons. The main factors implicated in Alzheimer’s disease including accumulation of misfolded and aggregated proteins (hyperphosphorylated microtubule associated protein referred to as tau and amyloid Aβ), oxidative damage, inflammation, mitochondrial impairments and chronic energy imbalance, chronic endoplasmic reticulum stress, autophagy dysfunction, the abnormality and dysfunction of the mitochondrion-associated endoplasmic reticulum membrane serving as bridges between endoplasmic reticulum and mitochondria and regulating multiple functions such as Ca2+ transfer, energy exchange, lipid synthesis and transports and protein folding, genetic variation in lysosomal genes, metabolomic changes are shortly considered. A special emphasis was placed on mitochondrial fission (fragmentation) is a prominent early event preceding Alzheimer’s disease pathology in transgenic Aβ-animal models, as well as on marked decrease in extracellular amyloid deposition, prevention of the cognitive deficit development and improvement of synaptic parameters after inhibiting abnormalities in mitochondrial dynamics. The important role of the well-characterized Saccharomyces cerevisiae yeast as a valuable eukaryotic model organism in unraveling complex fundamental intracellular mechanisms underlying Alzheimer’s disease is highlighted. The benefits of applying a new model organism the yeast Yarrowia lipolytica, an obligate aerobe with the respiratory metabolism closely resembling that of mammalian cells, amenable to both classical and molecular genetic techniques, having a long history of use as a producer of heterological proteins, possessing an ability to change its morphology (from yeast-like to true mycelium) in response to environmental conditions as an useful alternative in deciphering a role of mitochondrial dynamics and distribution in an yeast model of Alzheimer’s disease are suggested.
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