Department of Medicine, Division of Allergy, Immunology and Rheumatology, Buffalo General Hospital, University at Buffalo, State University of New York at Buffalo, 311 MultiLab Research Building, Buffalo, NY,14203, USA.
J Clin Immunol. 2009 Sep;29(5):646-56. doi: 10.1007/s10875-009-9309-5. Epub 2009 Jun 20.
We used proteomic analyses to assess how drug abuse modulates immunologic responses to infections with the human immunodeficiency virus type 1 (HIV-1).
Two-dimensional difference gel electrophoresis was utilized to determine changes in the proteome of peripheral blood mononuclear cells (PBMC) isolated from HIV-1-positive donors that occurred after treatment with cocaine or methamphetamine. Both drugs differentially regulated the expression of several functional classes of proteins. We further isolated specific subpopulations of PBMC to determine which subpopulations were selectively affected by treatment with drugs of abuse. Monocytes, B cells, and T cells were positively or negatively selected from PBMC isolated from HIV-1-positive donors.
Our results demonstrate that cocaine and methamphetamine modulate gene expression primarily in monocytes and T cells, the primary targets of HIV-1 infection. Proteomic data were validated with quantitative, real-time polymerase chain reaction. These studies elucidate the molecular mechanisms underlying the effects of drugs of abuse on HIV-1 infections. Several functionally relevant classes of proteins were identified as potential mediators of HIV-1 pathogenesis and disease progression associated with drug abuse.
我们使用蛋白质组学分析来评估药物滥用如何调节对人类免疫缺陷病毒 1 型 (HIV-1) 感染的免疫反应。
利用二维差异凝胶电泳来确定从 HIV-1 阳性供体分离的外周血单核细胞 (PBMC) 中的蛋白质组在接受可卡因或甲基苯丙胺治疗后发生的变化。两种药物都不同程度地调节了几种功能蛋白类的表达。我们进一步分离了 PBMC 的特定亚群,以确定哪些亚群受到滥用药物治疗的选择性影响。从 HIV-1 阳性供体分离的 PBMC 中,我们采用正选或负选的方法分离单核细胞、B 细胞和 T 细胞。
我们的结果表明,可卡因和甲基苯丙胺主要在单核细胞和 T 细胞中调节基因表达,这是 HIV-1 感染的主要靶细胞。蛋白质组学数据用定量实时聚合酶链反应进行了验证。这些研究阐明了滥用药物对 HIV-1 感染影响的分子机制。确定了几类具有功能相关性的蛋白质,它们可能是与药物滥用相关的 HIV-1 发病机制和疾病进展的潜在介质。