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阿尔茨海默病患者外周血淋巴细胞中8-氧代鸟嘌呤糖基化酶1基因的表达、多态性及氧化性DNA损伤水平

Expression and polymorphisms of gene 8-oxoguanine glycosylase 1 and the level of oxidative DNA damage in peripheral blood lymphocytes of patients with Alzheimer's disease.

作者信息

Dorszewska Jolanta, Kempisty Bartosz, Jaroszewska-Kolecka Joanna, Rózycka Agata, Florczak Jolanta, Lianeri Margarita, Jagodziński Paweł P, Kozubski Wojciech

机构信息

Laboratory of Neurobiology, Department of Neurology, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

DNA Cell Biol. 2009 Nov;28(11):579-88. doi: 10.1089/dna.2009.0926.

Abstract

The purpose of this study was to determine the level of 8-oxo-2'-deoxyguanosine (8-oxo2dG) and expression of three isoforms of 8-oxoguanine glycosylase 1 (OGG1), OGG1-1a, 1b, and 1c, and OGG1 protein and Ser326Cys and Arg46Gln polymorphisms of the OGG1 gene, in peripheral blood lymphocytes of patients with Alzheimer's disease (AD) and healthy controls. The study was performed in 41 AD patients and 51 healthy subjects. The level of 8-oxo2dG was determined by high performance liquid chromatography/electrochemical; expression of OGG1-1a, 1b, and 1c by real-time quantitative polymerase chain reaction; and OGG1 protein by Western blotting. The polymerase chain reaction-restriction fragment length polymorphism analysis was conducted to analyze the Ser326Cys and Arg46Gln polymorphisms. It was found that AD patients and controls have three isoforms, OGG1-1a, 1b, and 1c. The OGG1-1c isoform seems to be associated with early stage of AD, while an increase in the expression of the OGG1-1b isoform and levels of OGG1 protein appears to be similarly related to the progression of AD. All of the studied OGG1 isoforms show a decreased expression in advanced AD. The CG Ser326Cys genotype seems to have a tendency to decrease 8-oxo2dG via control of repair mechanisms. The Arg46Gln polymorphism is not associated with the pathogenesis of AD. It appears that the OGG1-1a, 1b, and 1c isoforms are involved in the pathogenesis of AD.

摘要

本研究旨在测定阿尔茨海默病(AD)患者和健康对照者外周血淋巴细胞中8-氧代-2'-脱氧鸟苷(8-oxo2dG)的水平、8-氧代鸟嘌呤糖基化酶1(OGG1)三种同工型OGG1-1a、1b和1c的表达、OGG1蛋白以及OGG1基因的Ser326Cys和Arg46Gln多态性。该研究纳入了41例AD患者和51例健康受试者。采用高效液相色谱/电化学法测定8-oxo2dG水平;采用实时定量聚合酶链反应测定OGG1-1a、1b和1c的表达;采用蛋白质免疫印迹法测定OGG1蛋白。通过聚合酶链反应-限制性片段长度多态性分析来分析Ser326Cys和Arg46Gln多态性。结果发现,AD患者和对照者均有OGG1-1a、1b和1c三种同工型。OGG1-1c同工型似乎与AD的早期阶段相关,而OGG1-1b同工型表达的增加和OGG1蛋白水平的升高似乎与AD的进展同样相关。所有研究的OGG1同工型在晚期AD中均表现出表达降低。CG Ser326Cys基因型似乎有通过控制修复机制降低8-oxo2dG的趋势。Arg46Gln多态性与AD的发病机制无关。看来OGG1-1a、1b和1c同工型参与了AD的发病机制。

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