Exposure of Normal Monocyte‐Derived Dendritic Cells to Human Immunodeficiency Virus Type‐1 Particles Leads to the Induction of Apoptosis in Co‐Cultured CD4+ as Well as …

S Suzuki, M Tobiume, M Kameoka… - Microbiology and …, 2000 - Wiley Online Library
S Suzuki, M Tobiume, M Kameoka, K Sato, TA Takahashi, T Mukai, K Ikuta
Microbiology and immunology, 2000Wiley Online Library
The depletion of immune T cells by human immunodeficiency virus type‐1 (HIV‐1) infection
is a major mechanism involved in the pathogenesis of AIDS. Here, we examined a possible
effector function of blood monocyte‐derived dendritic cells (DCs) to induce apoptosis in
bystander CD4+ and CD8+ T cells. The DCs were generated by culturing monocytes in the
presence of granulocyte‐macrophage colony‐stimulating factor and interleukin‐4. The DCs
exposed to HIV‐1 particles were co‐cultured with healthy donor‐derived blood T cells at a …
Abstract
The depletion of immune T cells by human immunodeficiency virus type‐1 (HIV‐1) infection is a major mechanism involved in the pathogenesis of AIDS. Here, we examined a possible effector function of blood monocyte‐derived dendritic cells (DCs) to induce apoptosis in bystander CD4+ and CD8+ T cells. The DCs were generated by culturing monocytes in the presence of granulocyte‐macrophage colony‐stimulating factor and interleukin‐4. The DCs exposed to HIV‐1 particles were co‐cultured with healthy donor‐derived blood T cells at a ratio of 1:20. Analyses by percent cell mortality, staining with propidium iodide and reactivity with Annexin V revealed the induction of apoptosis in both CD4+ and CD8+ target T cells. Further, this apoptosis occurred without stimulation with mitogens when the cell cycle of target T cells shifted from G0 to G1, probably due to the mitogenic effect of the DCs. Thus, induction of apoptosis in both CD4+ and CD8+ T cells occurred via interaction with DCs adsorbed with HIV‐1 particles.
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