Regulation of neuronal energy metabolism by calcium: Role of MCU and Aralar/malate-aspartate shuttle.

Calcium is a major regulator of cellular metabolism. Calcium controls mitochondrial respiration, and calcium signaling is used to meet cellular energetic demands through energy production in the organelle. Although it has been widely assumed that Ca ²⁺ -actions require its uptake by mitochondrial calcium uniporter (MCU), alternative pathways modulated by cytosolic Ca ²⁺ have been recently proposed. Recent findings have indicated a role for cytosolic Ca ²⁺ signals acting on mitochondrial NADH shuttles in the control of cellular metabolism in neurons using glucose as fuel. It has been demonstrated that AGC1/Aralar, the component of the malate/aspartate shuttle (MAS) regulated by cytosolic Ca ²⁺ , participates in the maintenance of basal respiration exerted through Ca ²⁺ -fluxes between ER and mitochondria, whereas mitochondrial Ca ²⁺ -uptake by MCU does not contribute. Aralar/MAS pathway, activated by small cytosolic Ca ²⁺ signals, provides in fact substrates, redox equivalents and pyruvate, fueling respiration. Upon activation and increases in workload, neurons upregulate OxPhos, cytosolic pyruvate production and glycolysis, together with glucose uptake, in a Ca ²⁺ -dependent way, and part of this upregulation is via Ca ²⁺ signaling. Both MCU and Aralar/MAS contribute to OxPhos upregulation, Aralar/MAS playing a major role, especially at small and submaximal workloads. Ca ²⁺ activation of Aralar/MAS, by increasing cytosolic NAD ⁺ /NADH provides Ca ²⁺ -dependent increases in glycolysis and cytosolic pyruvate production priming respiration as a feed-forward mechanism in response to workload. Thus, except for glucose uptake, these processes are dependent on Aralar/MAS, whereas MCU is the relevant target for Ca ²⁺ signaling when MAS is bypassed, by using pyruvate or β-hydroxybutyrate as substrates.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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