Labaratory of Molecular Virology, Division of Emerging and Transfusion Transmitted Diseases, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892, USA.
Mol Cell Biochem. 2010 Apr;337(1-2):175-83. doi: 10.1007/s11010-009-0297-9. Epub 2009 Oct 20.
Human immunodeficiency virus (HIV) infection-induced apoptosis of infected CD4 T cells as well as uninfected (bystander) CD4 T cells and other types of cells is a major factor in the pathogenesis of AIDS. Clinically, HIV-2 patients have a higher CD4 cell count at the time of an AIDS diagnosis, and generally have longer survival after development of symptoms. The mortality after an AIDS diagnosis has been reported to be more influenced by CD4 cell count than HIV type. Previous studies have shown significant variations in cytopathic effects following in vitro infection with primary isolates of HIV-1 or HIV-2 subtypes; however, the relative contributions of HIV-1 and HIV-2 infection leading to cell death remain unclear. Using a human cell line, Jurkat, we examined differences in key molecules involved in apoptotic signaling pathways during infection with either HIV-1 or HIV-2. HIV-1 infection generated more reactive oxygen species (ROS), increased the expression of a larger number of molecules involved in cell signaling such as p47, p38alpha, JNK, c-Yes, total PKC, and decreased the expression of molecules such as p38beta, ERK1/2, and XIAP relative to HIV-2 infection. HIV-1 induced a higher degree of cell death through stronger activation of both apoptotic pathways. HIV-1 infection downregulated both Bcl-X(L) and FLIP expressions at later time points postinfection, while HIV-2 infection dramatically upregulated both Bcl-X(L) and FLIP expression. We also found that the expression of Bcl-X(L) or FLIP resulted in significant inhibition of HIV replication in Jurkat cells. These findings suggest that HIV-1 infection with high levels of cytotoxicity results in a higher level of cell death through apoptosis during a short time postinfection. The longer period of infection observed with HIV-2 with a lower degree of cytotoxicity was accompanied by increased Bcl-X(L) and FLIP expression. High protein levels of Bcl-X(L) or FLIP inhibit HIV replication and may be one explanation for the clinical observation that HIV-2 infected patients generally tend to be long-term nonprogressors with high CD4 lymphocyte counts compared with HIV-1 infected persons.
人类免疫缺陷病毒(HIV)感染诱导感染的 CD4 T 细胞以及未感染的(旁观者)CD4 T 细胞和其他类型的细胞凋亡,是艾滋病发病机制的一个主要因素。临床上,HIV-2 患者在艾滋病诊断时的 CD4 细胞计数较高,并且在出现症状后通常具有更长的生存时间。艾滋病诊断后的死亡率据报道受 CD4 细胞计数的影响比 HIV 类型更大。先前的研究表明,HIV-1 或 HIV-2 亚型的原发性分离物体外感染后细胞病变效应存在显著差异;然而,HIV-1 和 HIV-2 感染导致细胞死亡的相对贡献尚不清楚。使用人细胞系 Jurkat,我们研究了感染 HIV-1 或 HIV-2 时参与凋亡信号通路的关键分子的差异。与 HIV-2 感染相比,HIV-1 感染产生更多的活性氧(ROS),增加了更多参与细胞信号转导的分子的表达,如 p47、p38alpha、JNK、c-Yes、总 PKC,并且降低了 p38beta、ERK1/2 和 XIAP 等分子的表达。与 HIV-2 感染相比,HIV-1 感染通过更强的两条凋亡途径的激活导致更高程度的细胞死亡。HIV-1 感染在感染后后期下调了 Bcl-X(L)和 FLIP 的表达,而 HIV-2 感染则显著上调了 Bcl-X(L)和 FLIP 的表达。我们还发现,Bcl-X(L)或 FLIP 的表达导致 Jurkat 细胞中 HIV 复制的显著抑制。这些发现表明,在感染后短时间内,高细胞毒性的 HIV-1 感染导致通过凋亡导致更高水平的细胞死亡。观察到的具有较低细胞毒性的 HIV-2 的更长感染期伴随着 Bcl-X(L)和 FLIP 表达的增加。Bcl-X(L)或 FLIP 的高蛋白水平抑制 HIV 复制,这可能是 HIV-2 感染患者与 HIV-1 感染患者相比,一般倾向于长期非进展者且 CD4 淋巴细胞计数较高的临床观察的一个解释。