• Ronan Astin, Robert Bentham, Siamak Djafarzadeh, James A Horscroft, Rhoda E Kuc, Po Sing Leung, James R A Skipworth, Jose M Vicencio, Anthony P Davenport, Andrew J Murray, Jukka Takala, Stephan M Jakob, Hugh Montgomery, and Gyorgy Szabadkai.
• 1] Department of Cell and Developmental Biology, Consortium for Mitochondrial Research, University College London, London, United Kingdom [2] Institute for Human Health and Performance, University College London, London, United Kingdom.
• Sci Rep. 2013 Jan 1;3:2467.

AbstractThe circulating, endocrine renin-angiotensin system (RAS) is important to circulatory homeostasis, while ubiquitous tissue and cellular RAS play diverse roles, including metabolic regulation. Indeed, inhibition of RAS is associated with improved cellular oxidative capacity. Recently it has been suggested that an intra-mitochondrial RAS directly impacts on metabolism. Here we sought to rigorously explore this hypothesis. Radiolabelled ligand-binding and unbiased proteomic approaches were applied to purified mitochondrial sub-fractions from rat liver, and the impact of AngII on mitochondrial function assessed. Whilst high-affinity AngII binding sites were found in the mitochondria-associated membrane (MAM) fraction, no RAS components could be detected in purified mitochondria. Moreover, AngII had no effect on the function of isolated mitochondria at physiologically relevant concentrations. We thus found no evidence of endogenous mitochondrial AngII production, and conclude that the effects of AngII on cellular energy metabolism are not mediated through its direct binding to mitochondrial targets.

17 keywords...

hide…