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阿尔茨海默病中蛋白质合成机制的改变:从核仁到核糖体

Altered Machinery of Protein Synthesis in Alzheimer's: From the Nucleolus to the Ribosome.

作者信息

Hernández-Ortega Karina, Garcia-Esparcia Paula, Gil Laura, Lucas José J, Ferrer Isidre

机构信息

Institute of Neuropathology, Service of Pathologic Anatomy, IDIBELL-Bellvitge University Hospital, University of Barcelona, Hospitalet de Llobregat, Spain.

Neuropathology, CIBERNED (Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas), Madrid, Spain.

出版信息

Brain Pathol. 2016 Sep;26(5):593-605. doi: 10.1111/bpa.12335. Epub 2015 Dec 14.

Abstract

Ribosomes and protein synthesis have been reported to be altered in the cerebral cortex at advanced stages of Alzheimer's disease (AD). Modifications in the hippocampus with disease progression have not been assessed. Sixty-seven cases including middle-aged (MA) and AD stages I-VI were analyzed. Nucleolar chaperones nucleolin, nucleophosmin and nucleoplasmin 3, and upstream binding transcription factor RNA polymerase I gene (UBTF) mRNAs are abnormally regulated and their protein levels reduced in AD. Histone modifications dimethylated histone H3K9 (H3K9me2) and acetylated histone H3K12 (H3K12ac) are decreased in CA1. Nuclear tau declines in CA1 and dentate gyrus (DG), and practically disappears in neurons with neurofibrillary tangles. Subunit 28 ribosomal RNA (28S rRNA) expression is altered in CA1 and DG in AD. Several genes encoding ribosomal proteins are abnormally regulated and protein levels of translation initiation factors eIF2α, eIF3η and eIF5, and elongation factor eEF2, are altered in the CA1 region in AD. These findings show alterations in the protein synthesis machinery in AD involving the nucleolus, nucleus and ribosomes in the hippocampus in AD some of them starting at first stages (I-II) preceding neuron loss. These changes may lie behind reduced numbers of dendritic branches and reduced synapses of CA1 and DG neurons which cause hippocampal atrophy.

摘要

据报道,在阿尔茨海默病(AD)晚期,大脑皮层中的核糖体和蛋白质合成会发生改变。尚未评估疾病进展过程中海马体的变化。对67例病例进行了分析,包括中年(MA)和AD的I - VI期。核仁伴侣蛋白核仁素、核磷蛋白和核质蛋白3,以及上游结合转录因子RNA聚合酶I基因(UBTF)的mRNA受到异常调节,且它们在AD中的蛋白质水平降低。CA1区中组蛋白修饰二甲基化组蛋白H3K9(H3K9me2)和乙酰化组蛋白H3K12(H3K12ac)减少。核内tau蛋白在CA1区和齿状回(DG)中减少,在有神经原纤维缠结的神经元中几乎消失。AD中CA1区和DG区的28核糖体RNA亚基(28S rRNA)表达发生改变。几个编码核糖体蛋白的基因受到异常调节,AD中CA1区翻译起始因子eIF2α、eIF3η和eIF5以及延伸因子eEF2的蛋白质水平发生改变。这些发现表明,AD中蛋白质合成机制存在改变,涉及AD海马体中的核仁、细胞核和核糖体,其中一些变化始于神经元丢失之前的早期阶段(I - II期)。这些变化可能是CA1区和DG区神经元树突分支数量减少以及突触减少导致海马萎缩的原因。

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