Ca2+-dependent modulation of GABAA and NMDA receptors by extracellular ATP: implication for function of tripartite synapse

Biochem Soc Trans. 2009 Dec;37(Pt 6):1407-11. doi: 10.1042/BST0371407.

Abstract

The importance of communication between neuronal and glial cells for brain function is recognized by a modern concept of 'tripartite synapse'. Astrocytes enwrap synapses and can modulate their activity by releasing gliotransmitters such as ATP, glutamate and D-serine. One of the regulatory pathways in the tripartite synapse is mediated by P2X purinoreceptors. Release of ATP from synaptic terminals and astrocytes activates Ca(2+) influx via P2X purinoreceptors which co-localize with NMDA (N-methyl-D-aspartate) and GABA (gamma-aminobutyric acid) receptors and can modulate their activity via intracellular cascades which involve phosphatase II and PKA (protein kinase A).

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Astrocytes / metabolism
  • Calcium / metabolism*
  • Humans
  • Mice
  • Neurons / metabolism
  • Presynaptic Terminals / metabolism
  • Receptors, GABA-A / metabolism*
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Receptors, Purinergic P2 / metabolism
  • Signal Transduction / physiology
  • Synapses / metabolism*

Substances

  • Receptors, GABA-A
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Purinergic P2
  • Adenosine Triphosphate
  • Calcium