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Identification of a potential HIV-induced source of bystander-mediated apoptosis in T cells: Upregulation of TRAIL in primary human macrophages by HIV-1 tat

  • Original Paper
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Journal of Biomedical Science

Abstract

The induction of apoptosis in T cells by bystander cells has been repeatedly implicated as a mechanism contributing to the T cell depletion seen in HIV infection. It has been shown that apoptosis could be induced in T cells from asymptomatic HIV-infected individuals in a Fas-independent, TNF-related apoptosis-inducing ligand (TRAIL)-dependent manner if the cells were pretreated with anti-CD3. It has also been shown that T cells from HIV-infected patients were even more sensitive to TRAIL induction of apoptosis than they were to Fas induction. Recently, it has been reported that in an HIV-1 SCID-Hu model, the vast majority of the T cell apoptosis is not associated with p24 and is therefore produced by bystander effects. Furthermore, few apoptotic cells were associated with neighboring cells which were positive for either Fas ligand or TNF. However, most of the apoptotic cells were associated with TRAIL-positive cells. The nature of these TRAIL-positive cells was undetermined. Here, we report that HIV infection of primary human macrophages switches on abundant TRAIL production both at the RNA and protein levels. Furthermore, more macrophages produce TRAIL than are infected by HIV, indicating that a bystander mechanism may, at least in part, upregulate TRAIL. Exogenously supplied HIV-1 Tat protein upregulates TRAIL production by primary human macrophages to an extent indistinguishable from infection. The results suggest a model in which HIV-1-infected cells produce extracellular Tat protein, which in turn upregulates TRAIL in macrophages which then can induce apoptosis in bystander T cells.

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Authors and Affiliations

  1. Division of Emerging and Transfusion Transmitted Diseases Office of Blood Research and Review, Center for Biologics Evaluation and Research, FDA HFM 315, 1401 Rockville Pike, 20182-1448, Rockville, MD, USA

    Mingjie Zhang, Xingxiang Li, Xiaowu Pang, Linna Ding, Owen Wood, Indira Hewlett & Andrew I. Dayton

  2. Division of Monoclonal Antibodies, Office of Therapeutics Research and Review, Center for Biologics Evaluation and Research, FDA, Rockville, Md., USA

    Kathlene Clouse

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  1. Mingjie Zhang
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  2. Xingxiang Li
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Zhang, M., Li, X., Pang, X. et al. Identification of a potential HIV-induced source of bystander-mediated apoptosis in T cells: Upregulation of TRAIL in primary human macrophages by HIV-1 tat. J Biomed Sci 8, 290–296 (2001). https://doi.org/10.1007/BF02256603

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  • DOI: https://doi.org/10.1007/BF02256603

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