[HTML][HTML] Uncoupling protein-1 is not leaky

IG Shabalina, M Ost, N Petrovic, M Vrbacky… - … et Biophysica Acta (BBA …, 2010 - Elsevier
IG Shabalina, M Ost, N Petrovic, M Vrbacky, J Nedergaard, B Cannon
Biochimica et Biophysica Acta (BBA)-Bioenergetics, 2010Elsevier
The activity of uncoupling protein-1 (UCP1) is rate-limiting for nonshivering thermogenesis
and diet-induced thermogenesis. Characteristically, this activity is inhibited by GDP
experimentally and presumably mainly by cytosolic ATP within brown-fat cells. The issue as
to whether UCP1 has a residual proton conductance even when fully saturated with
GDP/ATP (as has recently been suggested) has not only scientific but also applied interest,
since a residual proton conductance would make overexpressed UCP1 weight-reducing …
The activity of uncoupling protein-1 (UCP1) is rate-limiting for nonshivering thermogenesis and diet-induced thermogenesis. Characteristically, this activity is inhibited by GDP experimentally and presumably mainly by cytosolic ATP within brown-fat cells. The issue as to whether UCP1 has a residual proton conductance even when fully saturated with GDP/ATP (as has recently been suggested) has not only scientific but also applied interest, since a residual proton conductance would make overexpressed UCP1 weight-reducing even without physiological/pharmacological activation. To examine this question, we have here established optimal conditions for studying the bioenergetics of wild-type and UCP1(−/−) brown-fat mitochondria, analysing UCP1-mediated differences in parallel preparations of brown-fat mitochondria from both genotypes. Comparing different substrates, we find that pyruvate (or palmitoyl-l-carnitine) shows the largest relative coupling by GDP. Comparing albumin concentrations, we find the range 0.1–0.6% optimal; higher concentrations are inhibitory. Comparing basic medium composition, we find 125mM sucrose optimal; an ionic medium (50–100mM KCl) functions for wild-type but is detrimental for UCP1(−/−) mitochondria. Using optimal conditions, we find no evidence for a residual proton conductance (not a higher post-GDP respiration, a lower membrane potential or an altered proton leak at highest common potential) with either pyruvate or glycerol-3-phosphate as substrates, nor by a 3–4-fold alteration of the amount of UCP1. We could demonstrate that certain experimental conditions, due to respiratoty inhibition, could lead to the suggestion that UCP1 possesses a residual proton conductance but find that under optimal conditions our experiments concur with implications from physiological observations that in the presence of inhibitory nucleotides, UCP1 is not leaky.
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