hiv -1感染者淋巴细胞中bcl-2的差异表达和程序性细胞死亡易感性

Thomas S. Dobmeyer , Stefan A. Klein , Jürgen M. Dobmeyer , Bernhard Raffel , Stephan Findhammer , Dieter Hoelzer , Eilke B. Helm , Rita Rossol , Dieter Kabelitz
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引用次数: 8

摘要

bcl-2原癌基因编码线粒体内膜蛋白,阻断程序性细胞死亡。越来越多的证据表明,调节bcl-2的表达是正常淋巴细胞生死的决定因素。在这项研究中,我们用流式细胞术检测了人类免疫缺陷病毒1型(HIV-1)感染和健康受试者淋巴细胞中bcl-2的表达。在健康和hiv感染者的外周血淋巴细胞中检测到超过97%的bcl-2表达。一致观察到,低于200个CD4+细胞/μl的hiv -1感染者的CD4+淋巴细胞表达明显低于健康对照组。相比之下,bcl-2在这些患者的CD8+淋巴细胞中的表达明显增强。健康个体的淋巴细胞在多种调节细胞因子的存在下被多克隆激活时,bcl-2的表达未见明显变化。凋亡细胞的表达明显低于活细胞。凋亡细胞染色显示,hiv -1感染者的淋巴细胞对程序性细胞死亡的易感性增加,这种易感性并不局限于特定的淋巴细胞亚群。CD4+细胞/μl≤200的hiv -1感染者CD4+和CD8+淋巴细胞中bcl-2的表达差异有统计学意义,但对细胞凋亡的易感性差异无统计学意义。因此,我们得出结论,体外诱导细胞凋亡的敏感性或耐药性与bcl-2的表达没有直接关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Expression ofbcl-2and Susceptibility to Programmed Cell Death in Lymphocytes of HIV-1-Infected Individuals

Thebcl-2protooncogene encodes an inner mitochondrial membrane protein that blocks programmed cell death. There is now increasing evidence that regulation ofbcl-2expression is a determinant of life or death in normal lymphocytes. In this study, we examinedbcl-2expression in lymphocytes from human immunodeficiency virus type 1 (HIV-1)-infected and healthy subjects by flow cytometry.bcl-2expression was detected in more than 97% of peripheral blood lymphocytes in both healthy and HIV-infected individuals. It was consistently observed that CD4+ lymphocytes from HIV-1-infected individuals with less than 200 CD4+ cells/μl expressed significantly lessbcl-2than healthy controls. In contrast,bcl-2expression in CD8+ lymphocytes of these patients was significantly enhanced. No significant alteration ofbcl-2expression was found when lymphocytes of healthy individuals were polyclonally activated in the presence of various regulatory cytokines. Cells undergoing apoptosis showed significantly lowerbcl-2expression than viable cells. Staining of apoptotic cells revealed that lymphocytes from HIV-1-infected subjects were characterized by an increased susceptibility to programmed cell death which was not restricted to a particular lymphocyte subset. Despite significantly differentbcl-2expression in CD4+ and CD8+ lymphocytes of HIV-1-infected individuals with less than 200 CD4+ cells/μl, no difference could be observed concerning their susceptibility to undergo apoptosis. Therefore, we conclude that sensitivity or resistance toin vitroinduction of apoptosis does not directly correlate withbcl-2expression.

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