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Why are the neurodegenerative disease-related pathways overrepresented in primary HIV-infected peripheral blood mononuclear cells: a genome-wide perspective

机译:为什么在原发性HIV感染的外周血单核细胞中神经退行性疾病相关的通路过高:全基因组视角

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We demonstrate for the first time that the genome-wide profiling of HIV-infected peripheral blood mononuclear cells (PBMCs) from HIV-patients free of neurologic disease show overrepresentation of neurodegenerative pathways (Alzheimer’s, Parkinson’s, ALS, Huntington’s and Prion Disease, etc.) in genome-wide microarray analysis, which suggests that this genome-wide representation of neurodegenerative diseases-related pathways in PBMCs could possibly be a subcellular manifestation of neurologic interference by HIV. Further, the cell-tagging analysis attested this belief showing the large majority of genes tagged with cells of monocyte and macrophage lineage, which are implicated in neuronal dysfunction in both viral and non-viral neurodegenerative diseases. Together, these findings suggest that the genomic interference of HIV with neurodegenerative pathways is not by chance, but may be an early sign of HIV-mediated sub-genomic and sub-cellular manifestation of neurologic disease. Moreover, these findings signify the utility of PBMC and genome-wide mapping of the host gene expression as a powerful tool in predicting possible early events in neurologic deterioration in HIV patients.
机译:我们首次证明,来自无神经系统疾病的HIV患者的HIV感染的外周血单核细胞(PBMC)的全基因组谱分析显示了神经退行性途径的过度代表(阿尔茨海默氏症,帕金森氏症,ALS,亨廷顿氏症和普林氏病等)。 )进行全基因组微阵列分析,这表明PBMC中神经退行性疾病相关途径的这种全基因组表达可能是HIV引起神经系统干扰的亚细胞表现。此外,细胞标记分析证明了这种信念,显示出用单核细胞和巨噬细胞谱系细胞标记的绝大多数基因,这些基因与病毒性和非病毒性神经退行性疾病的神经元功能障碍有关。总之,这些发现表明,HIV对神经退行性途径的基因组干扰不是偶然的,而可能是HIV介导的神经系统疾病的亚基因组和亚细胞表现的早期迹象。而且,这些发现表明PBMC的实用性和宿主基因表达的全基因组作图作为预测HIV患者神经系统恶化的可能早期事件的有力工具。

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