1887

Abstract

The murine proapoptotic protein Bax was expressed in to investigate its effect on cell survival and production of reactive oxygen species (ROS). Bax expression decreased the number of cells capable of growing and forming colonies, and it increased the number of cells producing ROS, as detected by both dihydrorhodamine 123 fluorescence and the intracellular content of SH groups. Mutation in the β-subunit of F-ATPase, or mitochondrial deficiency resulting from deletion of mtDNA (ρ mutant), increased the sensitivity to Bax, indicating that Bax cytotoxicity does not require mitochondrial respiratory-chain functions. The antiapoptotic protein Bcl-x, when co-expressed with Bax, localized to the mitochondria and prevented Bax cytotoxicity. However, this co-expression did not prevent the production of ROS. These data suggest that in cells expressing Bax, ROS are not the of cell death and that the antiapoptotic function of Bcl-x is not limited to its antioxidant property.

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2002-09-01
2020-03-29
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