Mitochondrial dysfunction and effect of antiglycolytic bromopyruvic acid in GL15 glioblastoma cells

作者：Macchioni Lara; Davidescu Magdalena; Sciaccaluga Miriam; Marchetti Cristina; Migliorati Graziella; Coaccioli Stefano; Roberti Rita; Corazzi Lanfranco^*; Castigli Emilia

来源：Journal of Bioenergetics and Biomembranes, 2011, 43(5): 507-518.

DOI：10.1007/s10863-011-9375-2

• GL15 cells
• Cytochrome c
• ROS
• Mitochondrial membrane potential
• Bromopyruvate
• Respiratory chain inhibitors

Most cancer cells, including GL15 glioblastoma cells, rely on glycolysis for energy supply. The effect of antiglycolytic bromopyruvate on respiratory parameters and viability of GL15 cells was investigated. Bromopyruvate caused Delta psi m and MTT collapse, ATP decrease, and cell viability loss without involving apoptotic or necrotic pathways. The autophagy marker LC3-II was increased. Delta psi m decrease was accompanied by reactive oxygen species (ROS) increase and cytochrome c (cyt c) disappearance, suggesting a link between free radical generation and intramitochondrial cyt c degradation. Indeed, the free radical inducer menadione caused a decrease in cyt c that was reversed by N-acetylcysteine. Cyt c is tightly bound to the inner mitochondrial membrane in GL15 cells, which may confer protein peroxidase activity, resulting in auto-oxidation and protein targeting to degradation in the presence of ROS. This process is directed towards impairment of the apoptotic cyt c cascade, although cells are committed to die.

• 出版日期2011-10