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胆固醇转运体 ABCA1 的表达增加与 AD 海马体痴呆严重程度高度相关。

Increased expression of cholesterol transporter ABCA1 is highly correlated with severity of dementia in AD hippocampus.

机构信息

Department of Neuroscience, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Brain Res. 2010 Mar 8;1318:167-77. doi: 10.1016/j.brainres.2010.01.006. Epub 2010 Jan 14.

DOI:10.1016/j.brainres.2010.01.006
PMID:20079340
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2826590/
Abstract

To gain insight into ATP-binding cassette transporter A1 (ABCA1) function and its potential role in AD pathology, we analyzed the expression of the cholesterol transporter ABCA1 in postmortem hippocampus from persons at different stages of dementia and AD associated neuropathology relative to cognitively intact normal donors by quantitative polymerase chain reaction (qPCR) and Western blot. In this study clinical dementia rating (CDR) scores were used as a measure of dementia severity, whereas, Braak neuropathological staging and neuritic plaque density were used as an index of the neuropathological progression of AD. Correlation analysis showed that ABCA1 mRNA expression was significantly elevated at the earliest recognizable stage of dementia compared to persons with intact cognition. ABCA1 mRNA was also positively correlated with Braak neuropathological stages and neuritic plaque density counts. Additionally, ABCA1 mRNA levels showed robust correlation with dementia severity even after controlling for the confounding contribution of accompanying neuropathological parameters to ABCA1 mRNA expression. Western blot analyses showed that the differential expression observed at the transcriptional level is also reflected at the protein level. Thus, our study provides transcriptional and translational evidence that the expression of ABCA1, a key modulator of cholesterol transport across the plasma membrane, is dysregulated in the AD brain and that this dysregulation is associated with increasing severity of AD, whether measured functionally as dementia severity or neuropathologically as increased neuritic plaque and neurofibrillary tangle density.

摘要

为了深入了解三磷酸腺苷结合盒转运体 A1(ABCA1)的功能及其在 AD 病理中的潜在作用,我们通过定量聚合酶链反应(qPCR)和 Western blot 分析了不同痴呆阶段和 AD 相关神经病理学患者死后海马体中胆固醇转运体 ABCA1的表达,与认知正常的正常供体进行比较。在这项研究中,临床痴呆评定量表(CDR)评分被用作痴呆严重程度的衡量标准,而 Braak 神经病理学分期和神经原纤维缠结密度则被用作 AD 神经病理学进展的指标。相关性分析表明,与认知正常的个体相比,ABCA1 mRNA 的表达在最早可识别的痴呆阶段显著升高。ABCA1 mRNA 也与 Braak 神经病理学分期和神经原纤维缠结密度计数呈正相关。此外,即使在控制伴随的神经病理学参数对 ABCA1 mRNA 表达的混杂影响后,ABCA1 mRNA 水平与痴呆严重程度也显示出很强的相关性。Western blot 分析表明,在转录水平上观察到的差异表达也反映在蛋白质水平上。因此,我们的研究提供了转录和翻译证据,表明 ABCA1 的表达,即跨细胞膜胆固醇转运的关键调节剂,在 AD 大脑中失调,并且这种失调与 AD 严重程度的增加有关,无论是通过痴呆严重程度的功能测量还是通过神经原纤维缠结和神经原纤维缠结密度的增加来进行神经病理学测量。

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