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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >ANALYSIS OF SNAP25 mRNA EXPRESSION AND PROMOTER DNA METHYLATION IN BRAIN AREAS OF ALZHEIMER'S DISEASE PATIENTS
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ANALYSIS OF SNAP25 mRNA EXPRESSION AND PROMOTER DNA METHYLATION IN BRAIN AREAS OF ALZHEIMER'S DISEASE PATIENTS

机译:老年性痴呆患者脑区SNAP25 mRNA表达及启动子DNA甲基化分析

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摘要

Alzheimer's Disease (AD) is the most common cause of dementia in elderly people. The presynaptic terminal is an important site of pathological changes in AD, leading to synaptic loss in specific brain regions, such as in the cortex and hippocampus. In this study, we investigated syn-aptosomal-associated protein, 25-kDa (SNAP25) mRNA levels and promoter DNA methylation in post mortem brain tissues (entorhinal and auditory cortices and hippocampus) from healthy elderly and AD subjects as well as in peripheral blood leukocytes of young, healthy elderly and AD patients. mRNA quantification was performed by quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR) using the DELTADELTAC_t method and promoter DNA methylation was quantified by mass spectrometry using the Sequenom EpiTYPER platform. We observed a significant decrease in SNAP25 expression in AD across all the three brain regions in relation to the healthy elderly subjects, suggesting impairment in synaptic function. The changes in the auditory cortex reflected those observed in the hippocampus and entorhinal cortex, the primary areas affected in AD. However, no AD-associated differences in SNAP25 promoter DNA methylation were observed suggesting that other mechanisms may be involved in mediating the observed gene expression changes.
机译:阿尔茨海默氏病(AD)是老年人痴呆症的最常见原因。突触前末端是AD病理变化的重要部位,导致特定大脑区域(例如皮质和海马区)的突触丢失。在这项研究中,我们调查了健康老年人和AD受试者的死后脑组织(肠和听觉皮层和海马)中的同核小体相关蛋白,25 kDa(SNAP25)mRNA水平和启动子DNA甲基化年轻,健康的老年人和AD患者的白细胞。使用DELTADELTAC_t方法通过定量逆转录聚合酶链反应(qRT-PCR)进行mRNA定量,并使用Sequenom EpiTYPER平台通过质谱对启动子DNA甲基化进行定量。我们观察到相对于健康的老年受试者,在所有三个大脑区域中,AD中的SNAP25表达均显着降低,表明突触功能受损。听觉皮层的变化反映了在AD受影响的主要区域海马和内嗅皮层中观察到的变化。但是,没有观察到与SNAP25启动子DNA甲基化相关的AD相关差异,表明其他机制可能与介导观察到的基因表达变化有关。

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