Astrocytes modulate neural network activity by Ca²+-dependent uptake of extracellular K+

Sci Signal. 2012 Apr 3;5(218):ra26. doi: 10.1126/scisignal.2002334.

Abstract

Astrocytes are electrically nonexcitable cells that display increases in cytosolic calcium ion (Ca²+) in response to various neurotransmitters and neuromodulators. However, the physiological role of astrocytic Ca²+ signaling remains controversial. We show here that astrocytic Ca²+ signaling ex vivo and in vivo stimulated the Na+,K+-ATPase (Na+- and K+-dependent adenosine triphosphatase), leading to a transient decrease in the extracellular potassium ion (K+) concentration. This in turn led to neuronal hyperpolarization and suppressed baseline excitatory synaptic activity, detected as a reduced frequency of excitatory postsynaptic currents. Synaptic failures decreased in parallel, leading to an increase in synaptic fidelity. The net result was that astrocytes, through active uptake of K+, improved the signal-to-noise ratio of synaptic transmission. Active control of the extracellular K+ concentration thus provides astrocytes with a simple yet powerful mechanism to rapidly modulate network activity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Animals, Newborn
  • Astrocytes / cytology
  • Astrocytes / metabolism
  • Astrocytes / physiology*
  • Biological Transport / drug effects
  • Calcium / metabolism*
  • Calcium Signaling / physiology
  • Cells, Cultured
  • Excitatory Postsynaptic Potentials / physiology
  • Extracellular Space / metabolism
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Confocal
  • Nerve Net / metabolism
  • Nerve Net / physiology
  • Neurons / cytology
  • Neurons / metabolism
  • Neurons / physiology
  • Ouabain / pharmacology
  • Potassium / metabolism*
  • Rats
  • Rats, Wistar
  • Receptors, G-Protein-Coupled / agonists
  • Receptors, G-Protein-Coupled / physiology
  • Rubidium Radioisotopes / metabolism
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Synaptic Transmission / physiology*

Substances

  • Receptors, G-Protein-Coupled
  • Rubidium Radioisotopes
  • Ouabain
  • Adenosine Triphosphate
  • Sodium-Potassium-Exchanging ATPase
  • Potassium
  • Calcium