Single-cell imaging of bioenergetic responses to neuronal excitotoxicity and oxygen and glucose deprivation

J Neurosci. 2014 Jul 30;34(31):10192-205. doi: 10.1523/JNEUROSCI.3127-13.2014.

Abstract

Excitotoxicity is a condition occurring during cerebral ischemia, seizures, and chronic neurodegeneration. It is characterized by overactivation of glutamate receptors, leading to excessive Ca(2+)/Na(+) influx into neurons, energetic stress, and subsequent neuronal injury. We and others have previously investigated neuronal populations to study how bioenergetic parameters determine neuronal injury; however, such experiments are often confounded by population-based heterogeneity and the contribution of effects of non-neuronal cells. Hence, we here characterized bioenergetics during transient excitotoxicity in rat and mouse primary neurons at the single-cell level using fluorescent sensors for intracellular glucose, ATP, and activation of the energy sensor AMP-activated protein kinase (AMPK). We identified ATP depletion and recovery to energetic homeostasis, along with AMPK activation, as surprisingly rapid and plastic responses in two excitotoxic injury paradigms. We observed rapid recovery of neuronal ATP levels also in the absence of extracellular glucose, or when glycolytic ATP production was inhibited, but found mitochondria to be critical for fast and complete energetic recovery. Using an injury model of oxygen and glucose deprivation, we identified a similarly rapid bioenergetics response, yet with incomplete ATP recovery and decreased AMPK activity. Interestingly, excitotoxicity also induced an accumulation of intracellular glucose, providing an additional source of energy during and after excitotoxicity-induced energy depletion. We identified this to originate from extracellular, AMPK-dependent glucose uptake and from intracellular glucose mobilization. Surprisingly, cells recovering their elevated glucose levels faster to baseline survived longer, indicating that the plasticity of neurons to adapt to bioenergetic challenges is a key indicator of neuronal viability.

Keywords: bioenergetics; excitotoxicity; single-cell imaging.

MeSH terms

  • Animals
  • Animals, Newborn
  • Calcium / metabolism
  • Cells, Cultured
  • Cerebellum / cytology
  • Cerebral Cortex / cytology
  • Deoxyglucose / pharmacokinetics
  • Energy Metabolism / physiology*
  • Glucose / deficiency*
  • Glucose / metabolism
  • Glutamic Acid / pharmacology
  • Glycine / toxicity
  • Hypoxia*
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Membrane Potential, Mitochondrial / drug effects
  • Membrane Potential, Mitochondrial / physiology
  • Mice
  • Neurons / drug effects
  • Neurons / physiology*
  • Neurotoxins / pharmacology
  • Optical Imaging*
  • Rats
  • Single-Cell Analysis

Substances

  • Luminescent Proteins
  • Neurotoxins
  • Glutamic Acid
  • Deoxyglucose
  • Glucose
  • Calcium
  • Glycine