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Gene expression profiles and protein–protein interaction network analysis in AIDS patients with HIV-associated encephalitis and dementia

机译:艾滋病合并HIV相关性脑炎和痴呆的AIDS患者的基因表达谱和蛋白-蛋白相互作用网络分析

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Central nervous system dysfunction is an important cause of morbidity and mortality in patients with human immunodeficiency virus type 1 (HIV-1) infection and acquired immunodeficiency virus syndrome (AIDS). Patients with AIDS are usually affected by HIV-associated encephalitis (HIVE) with viral replication limited to cells of monocyte origin. To examine the molecular mechanisms underlying HIVE-induced dementia, the GSE4755 Affymetrix data were obtained from the Gene Expression Omnibus database and the differentially expressed genes (DEGs) between the samples from AIDS patients with and without apparent features of HIVE-induced dementia were identified. In addition, protein–protein interaction networks were constructed by mapping DEGs into protein–protein interaction data to identify the pathways that these DEGs are involved in. The results revealed that the expression of 1,528 DEGs is mainly involved in the immune response, regulation of cell proliferation, cellular response to inflammation, signal transduction, and viral replication cycle. Heat-shock protein alpha, class A member 1 (HSP90AA1), and fibronectin 1 were detected as hub nodes with degree values >130. In conclusion, the results indicate that HSP90A and fibronectin 1 play important roles in HIVE pathogenesis.
机译:中枢神经系统功能障碍是1型人类免疫缺陷病毒(HIV-1)感染和后天免疫缺陷病毒综合征(AIDS)患者发病和死亡的重要原因。艾滋病患者通常受艾滋病毒相关脑炎(HIVE)的影响,病毒复制仅限于单核细胞来源的细胞。为了检查HIVE诱发痴呆的分子机制,从Gene Expression Omnibus数据库获得了GSE4755 Affymetrix数据,并鉴定了患有和没有HIVE诱发痴呆的明显特征的艾滋病患者样本之间的差异表达基因(DEG)。另外,通过将DEGs映射到蛋白质-蛋白质相互作用数据中以鉴定这些DEG参与的途径,构建了蛋白质-蛋白质相互作用网络。结果表明,1,528个DEG的表达主要参与免疫应答,细胞调节。增殖,细胞对炎症的反应,信号转导和病毒复制周期。检测到热休克蛋白alpha,A类成员1(HSP90AA1)和纤连蛋白1为度值> 130的中枢节点。总之,结果表明HSP90A和纤连蛋白1在HIVE发病机理中起重要作用。

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