Distinct Regulation of Bioenergetics and Translation by Gp I mGluR and NMDAR

Abstract

Neuronal activity is responsible for large energy consumption within the brain. However, the cellular mechanisms draining ATP upon the arrival of a stimulus are yet to be explored systematically at the post-synapse. Here we provide evidence that a significant fraction of ATP is consumed upon glutamate stimulation to energize the mGluR-induced protein synthesis. We find that both mGluR and NMDAR alter protein synthesis and ATP consumption with distinct kinetics at the synaptic-dendritic compartments. While mGluR activation leads to a rapid and sustained reduction in the neuronal ATP level, NMDAR activation has no immediate impact on the same. ATP consumption correlates inversely to the kinetics of protein synthesis for both the receptors. We observe a persistent elevation in protein synthesis within 5 minutes of mGluR activation and robust inhibition of the same within 2 minutes of NMDAR activation, assessed by the phosphorylation status of eEF2 and metabolic labeling. However, a delayed protein synthesis-dependent ATP expenditure ensues after 15 minutes of NMDAR activation. We identify a central role for AMPK in this correlation between protein synthesis and ATP consumption. AMPK is dephosphorylated and inhibited upon mGluR activation while it was rapidly phosphorylated upon NMDAR activation. Perturbing AMPK activity disrupts the receptor-specific modulations of eEF2 phosphorylation and protein synthesis. Therefore, our observations suggest that the glutamate receptors required modulating the AMPK-eEF2 signaling axis to alter neuronal protein synthesis and bioenergetics. Short SummaryStimulation of glutamate receptors induces robust protein synthesis within cortical neurons and consumes a significantly large fraction of cellular ATP. Glutamate receptors viz. mGlulR and NMDAR modulate AMPK-eEF2 signaling uniquely leading to the dynamic regulation of protein synthesis and bioenergetics. Key HighlightsO_LIProtein synthesis following glutamate receptor activation is responsible for the bulk of the activity-induced ATP consumption in cortical neurons. C_LIO_LImGluR and NMDAR regulate protein synthesis with distinct kinetics and dictate the subsequent impacts over neuronal ATP level. C_LIO_LIDynamic modulation of AMPK and eEF2 phosphorylation is key to create unique temporal features of receptor-specific protein synthesis and bioenergetics. C_LI