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      Human immunodeficiency virus type 1 protease cleaves procaspase 8 in vivo.

      Journal of Biology
      Antigens, CD27, Apoptosis, genetics, CD4-Positive T-Lymphocytes, enzymology, virology, CD8-Positive T-Lymphocytes, Caspase 8, metabolism, HIV Infections, HIV Protease, HIV-1, Humans, Immunologic Memory, Jurkat Cells

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          Abstract

          Human immunodeficiency virus type 1 (HIV-1) infection causes apoptosis of infected CD4 T cells as well as uninfected (bystander) CD4 and CD8 T cells. It remains unknown what signals cause infected cells to die. We demonstrate that HIV-1 protease specifically cleaves procaspase 8 to create a novel fragment termed casp8p41, which independently induces apoptosis. casp8p41 is specific to HIV-1 protease-induced death but not other caspase 8-dependent death stimuli. In HIV-1-infected patients, casp8p41 is detected only in CD4(+) T cells, predominantly in the CD27(+) memory subset, its presence increases with increasing viral load, and it colocalizes with both infected and apoptotic cells. These data indicate that casp8p41 independently induces apoptosis and is a specific product of HIV-1 protease which may contribute to death of HIV-1-infected cells.

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