Mitochondrial calcium drives clock gene-dependent activation of pyruvate dehydrogenase and of oxidative phosphorylation

Abstract

Regulation of metabolism is emerging as a major output of circadian clock circuitry in mammals. Accordingly, mitochondrial oxidative metabolism undergoes both in vivo and in vitro daily oscillatory activities. In a previous study we showed that both glycolysis and mitochondrial oxygen consumption display a similar time-resolved rhythmic activity in synchronized HepG2 cell cultures, which translates in overall bioenergetic changes as here documented by measurement of the ATP level. Treatment of synchronized cells with specific metabolic inhibitors unveiled pyruvate as a major source of reducing equivalents to the respiratory chain with its oxidation driven by the rhythmic (de)phosphorylation of pyruvate dehydrogenase. Further investigation enabled to causally link the autonomous cadenced mitochondrial respiration to a synchronous increase of the mitochondrial Ca²⁺. The rhythmic change of the mitochondrial respiration was dampened by inhibitors of the mitochondrial Ca²⁺ uniporter as well as of the ryanodine receptor Ca²⁺ channel or the ADPR cyclase, indicating that the mitochondrial Ca²⁺ influx originated from the ER store, likely at contact sites with the mitochondrial compartment. Notably, blockage of the mitochondrial Ca²⁺ influx resulted in deregulation of the expression of canonical clock genes such as BMALl1, CLOCK, NR1D1. All together our findings unveil a hitherto unexplored function of Ca²⁺-mediated signaling in time keeping the mitochondrial metabolism and in its feed-back modulation of the circadian clockwork.

Keywords: Circadian clock-genes; Inter-organelle communication; Mitochondria; Mitochondrial calcium signaling; Oxidative phosphorylation; Pyruvate dehydrogenase.