Mitochondrial sodium/calcium exchanger <scp>NCLX</scp> regulates glycolysis in astrocytes, impacting on cognitive performance
João Victor Cabral‐Costa, Carlos Vicente‐Gutiérrez, Jesús Agulla, Rebeca Lapresa, John W. Elrod, Ángeles Almeida, Juan P. Bolaños, Alicia J. Kowaltowski
Abstract
Abstract Intracellular Ca 2+ concentrations are strictly controlled by plasma membrane transporters, the endoplasmic reticulum, and mitochondria, in which Ca 2+ uptake is mediated by the mitochondrial calcium uniporter complex (MCUc), while efflux occurs mainly through the mitochondrial Na + /Ca 2+ exchanger (NCLX). RNAseq database repository searches led us to identify the Nclx transcript as highly enriched in astrocytes when compared with neurons. To assess the role of NCLX in mouse primary culture astrocytes, we inhibited its function both pharmacologically or genetically. This resulted in re‐shaping of cytosolic Ca 2+ signaling and a metabolic shift that increased glycolytic flux and lactate secretion in a Ca 2+ ‐dependent manner. Interestingly, in vivo genetic deletion of NCLX in hippocampal astrocytes improved cognitive performance in behavioral tasks, whereas hippocampal neuron‐specific deletion of NCLX impaired cognitive performance. These results unveil a role for NCLX as a novel modulator of astrocytic glucose metabolism, impacting on cognition. image