感染人脑中HIV-1 RNA拷贝数多剪接与非剪接比值的区域定量比较。

Robert K Fujimura, Imad Khamis, Paul Shapshak, Karl Goodkin
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引用次数: 7

摘要

HIV-1感染大脑通常会导致认知运动障碍,最严重的形式是HIV-1相关的痴呆(HAD)。然而,神经艾滋病在分子水平上的病因和发病机制仍不完全清楚,争议性问题仍然存在,包括流产感染和局部病毒载量的意义。本文提出,对HIV-1前病毒和RNAloads在大脑中的定量比较将澄清其中的一些问题。与先前发现的HIV-1病毒和毒株的脑区域差异相似,我们推测多剪接和未剪接HIV RNA在大脑不同区域的比例存在差异。采用竞争性RT-PCR方法比较了1例HAD患者脑区多剪接与未剪接HIV-1 RNA的比例。统计分析结果显示,各RNA制剂重复检测所得数据无显著差异。从大脑不同区域获得的样本之间发现了显著的差异。额叶MS/US RNA的比值明显大于基底节、内侧颞叶和颞叶的另一个部位。必须指出的是,我们的方法是对相隔几厘米的宏观大脑区域进行分析;未来的研究将分析这些大脑区域的显微分析。目前的研究是为了产生cm距离神经解剖位置的总体差异的结果。未来的研究将进行比较不同区域的微观解剖特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regional quantitative comparison of multispliced to unspliced ratios of HIV-1 RNA copy number in infected human brain.

Infection of the brain by HIV-1 often results in cognitive- motor disorders, the most severe form being HIV-1 associated dimentia (HAD). However, the etiology and pathogenesis of neuroAIDS at the molecular level is still not fully understood and controversial issues remain, including the significance of abortive infection and localized viral load. This paper proposes that quantitative comparison of HIV-1 proviral and RNAloads across the brain will clarify some of these issues. It was hypothesized that there are differences in ratios of multispliced and unspliced HIV RNA in different regions of brain by analogy with prior findings of brain regional differences in virus and strains of HIV-1. A competitive RT-PCR method was used to compare ratios of multispliced to unspliced HIV-1 RNA's across brain regions of one case with HAD. Statistical analysis results showed that data obtained by repeated assays for each RNA preparation were not significantly different. Significant differences were detected between specimens obtained from different regions of the brain. The ratio of MS/US RNA in the frontal lobe was significantly greater than in the basal ganglia, medial temporal lobe, and another site in the temporal lobe. It must be noted that our approach has been the analysis of macroscopic brain regions separated by several centimeters; future studies will analyze microscopic analysis of these brain regions. The current study was preformed to produce results on gross differences in neuroanatomical locations at cm distances. Future studies will be performed to compare different regions with microscopic anatomic specificity.

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