Uncoupling protein-3 lowers reactive oxygen species production in isolated mitochondria

• Published in: Free radical biology & medicine Vol. 49; no. 4; pp. 606 - 611
• Main Authors: Toime, Laurence J., Brand, Martin D.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.08.2010
• Subjects: Adenine nucleotide translocase; Animals; ANT; Ion Channels - deficiency; Ion Channels - isolation & purification; Ion Channels - metabolism; Membrane potential; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondria - chemistry; Mitochondria - metabolism; Mitochondrial Proteins - deficiency; Mitochondrial Proteins - isolation & purification; Mitochondrial Proteins - metabolism; Muscle, Skeletal - metabolism; Reactive oxygen species; Reactive Oxygen Species - metabolism; UCP3; Uncoupling protein; Uncoupling Protein 3; Mitochondria; Reactive oxygen species; Uncoupling protein; Adenine nucleotide translocase; UCP3; ANT; Membrane potential
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2010.05.010

Mitochondria are the major cellular producers of reactive oxygen species (ROS), and mitochondrial ROS production increases steeply with increased proton-motive force. The uncoupling proteins (UCP1, UCP2, and UCP3) and adenine nucleotide translocase induce proton leak in response to exogenously added fatty acids, superoxide, or lipid peroxidation products. “Mild uncoupling” by these proteins may provide a negative feedback loop to decrease proton-motive force and attenuate ROS production. Using wild-type and Ucp3 -/- mice, we found that native UCP3 actively lowers the rate of ROS production in isolated energized skeletal muscle mitochondria, in the absence of exogenous activators. The estimated specific activity of UCP3 in lowering ROS production was 90 to 500 times higher than that of the adenine nucleotide translocase. The mild uncoupling hypothesis was tested by measuring whether the effect of UCP3 on ROS production could be mimicked by chemical uncoupling. A chemical uncoupler mimicked the effect of UCP3 at early time points after mitochondrial energization, in support of the mild uncoupling hypothesis. However, at later time points the uncoupler did not mimic UCP3, suggesting that UCP3 can also affect ROS production through a membrane potential-independent mechanism.