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BCL-2 independent program in HLV envelope mediated programmed cell death.

Kolesnitchenko V, Donoghue ET, Korsmeyer SJ, Lane HC, Cohen DI; National Conference on Human Retroviruses and Related Infections.

Program Abstr First Natl Conf Hum Retrovir Relat Infect Natl Conf Hum Retrovir Relat Infect 1st 1993 Wash DC. 1993 Dec 12-16; 112.

NIH, Bethesda, MD.

To assess the role of the bcl-2 proto oncogene in the context of HIV envelope Mediated cell death, Jurkat T cell lines and Jurkat expressing the HIV envelope glycoproteins (HIV env) were transfected either with a SFFV-bcl-2-nl construct containing the complete human bcl-2 protein or a SFFV control construct. Eleven Jurkat and seven HIV env clones stably overexpressing bcl-2 protein with various levels of expression were selected. Apoptosis induced by serum starvation was decreased, and (3H) thymidine incorporation increased, in bcl-2 transfectants but not in control transfectants, establishing that overexpression of bcl-2 protein had functional consequences in Jurkat cells. HIV envelope CPE was examined in Jurkat cell lines overexpressing bcl-2 either following infection with HIV-1 (LAV), or following exposure to HIV envelope transfected cells in mixtures where either one or both partners overexpressed bcl-2 protein. In all cases cell killing associated with the nucleosomal DNA fragmentation characteristic of PCD persisted unchanged despite bcl-2 protein overexpression. Infection with HIV spread comparably in Jurkat cells overexpressing bcl-2, as in controls. The result that bcl-2 protein overexpression does not block HIV mediated-PCD establishes that at least one form of HIV killing proceeds by a bcl-2 independent pathway, thereby distinguishing HIV PCD from most forms of PCD used by developing thymocytes.

Publication Types:
  • Meeting Abstracts
Keywords:
  • Acquired Immunodeficiency Syndrome
  • Apoptosis
  • CASP4 protein, human
  • Caspases
  • Cell Line
  • Genes, env
  • HIV Infections
  • HIV Seropositivity
  • HIV-1
  • Humans
  • Jurkat Cells
  • T-Lymphocytes
  • genetics
Other ID:
  • 95921342
UI: 102214282

From Meeting Abstracts




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