Zhou Dejiang, Spector Stephen A
Department of Pediatrics, Division of Infectious Diseases, University of California San Diego, La Jolla, California, 92093-0672, USA.
AIDS. 2008 Mar 30;22(6):695-9. doi: 10.1097/QAD.0b013e3282f4a836.
Human immunodeficiency virus type-1 (HIV-1) induces a series of alterations in the host cell that modify the intracellular environment in favor of viral replication, survival and spread. This research examined the impact of HIV-1 infection on autophagy in HIV-1 infected cells.
Protein extracts of HIV-1 infected and control CD4+ T-lymphocytes and U937 cells were semi-quantified by western blot. The autophagy-related protein Beclin 1, a Bcl-2 associated protein, and the 16 kD microtubule-associated protein (MAP) light chain three (LC3) which is essential for autophagy were quantified and validated using the intracellular protein GAPDH as an internal standard. Beclin 1 mRNA was quantified by real-time reverse transcriptase-polymerase chain reaction. Autophagosomes were assessed by visualization under confocal microscopy following intracellular staining of the LC3 protein.
Following infection of human peripheral blood CD4+ T-cells or U937 cells with HIV-1 for 48 h, the autophagy protein Beclin 1 and LC3 II, which is essential for autophagy, were found to be markedly decreased. Beclin 1 mRNA expression was also reduced. Autophagosomes were reduced in HIV-1-infected cells. The reduction of autophagic protein expression and autophagosomes in HIV-1-infected cells could be overcome by amino acid starvation or rapamycin.
These data demonstrate that HIV-1 infection can down-regulate autophagy in infected cells during acute infection, and provide new insights into HIV-1-induced cell death and disease-related pathogenesis.
1型人类免疫缺陷病毒(HIV-1)可诱导宿主细胞发生一系列改变,从而改变细胞内环境以利于病毒复制、存活和传播。本研究检测了HIV-1感染对HIV-1感染细胞自噬的影响。
通过蛋白质印迹法对HIV-1感染的和对照的CD4+ T淋巴细胞及U937细胞的蛋白质提取物进行半定量分析。使用细胞内蛋白甘油醛-3-磷酸脱氢酶(GAPDH)作为内参,对自噬相关蛋白Beclin 1(一种与Bcl-2相关的蛋白)以及对自噬至关重要的16kD微管相关蛋白(MAP)轻链3(LC3)进行定量和验证。通过实时逆转录聚合酶链反应对Beclin 1 mRNA进行定量。在对LC3蛋白进行细胞内染色后,通过共聚焦显微镜观察来评估自噬体。
用HIV-1感染人外周血CD4+ T细胞或U937细胞48小时后,发现自噬蛋白Beclin 1和对自噬至关重要的LC3 II明显减少。Beclin 1 mRNA表达也降低。HIV-1感染的细胞中自噬体减少。氨基酸饥饿或雷帕霉素可克服HIV-1感染细胞中自噬蛋白表达和自噬体的减少。
这些数据表明,在急性感染期间,HIV-1感染可下调感染细胞中的自噬,并为HIV-1诱导的细胞死亡和疾病相关发病机制提供了新的见解。