Apoptotic GSH Extrusion Is Associated with Free Radical Generation

• Published in: Annals of the New York Academy of Sciences Vol. 1010; no. 1; pp. 449 - 452
• Main Authors: D'ALESSIO, M, CERELLA, C, DE NICOLA, M, BERGAMASCHI, A, MAGRINI, A, GUALANDI, G, ALFONSI, AM, GHIBELLI, L
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.12.2003
• Subjects: apoptosis; Apoptosis - drug effects; Apoptosis - physiology; Cell Hypoxia - physiology; Free Radicals - metabolism; glutathione; Glutathione - metabolism; Humans; Intracellular Membranes - drug effects; Intracellular Membranes - physiology; Membrane Potentials - drug effects; Membrane Potentials - physiology; Mitochondria - drug effects; Mitochondria - physiology; mitochondrial transmembrane potential; Puromycin - pharmacology; reactive oxygen species; Reactive Oxygen Species - metabolism; ROS; U937 Cells
• ISSN: 0077-8923; 1749-6632
• DOI: 10.1196/annals.1299.082

: Reactive oxygen species (ROS) are involved in many forms of apoptosis and mediate apoptosis in a number of cell types. In this paper, we use a variant of U937 monocytic cells (U937 HX) that show different biochemical features with respect to standard U937. Apoptotic standard U937 extrude reduced glutathione (GSH) and generate free radicals concomitantly with loss of mitochondria transmembrane potential (mt Δψ). These events are correlated with the extrusion of intracellular GSH. Conversely, apoptotic U937 HX cells retain GSH, and the loss of mt Δψ is not accompanied by generation of free radicals. The perfect inverse correlation between (a) ROS generation and (b) the presence of intracellular GSH during apoptosis suggests novel mechanisms to finely tune ROS generation in apoptosis.