Transporters for L-glutamate: an update on their molecular pharmacology and pathological involvement

Br J Pharmacol. 2007 Jan;150(1):5-17. doi: 10.1038/sj.bjp.0706949. Epub 2006 Nov 6.

Abstract

L-Glutamate (Glu) is the major excitatory neurotransmitter in the mammalian CNS and five types of high-affinity Glu transporters (EAAT1-5) have been identified. The transporters EAAT1 and EAAT2 in glial cells are responsible for the majority of Glu uptake while neuronal EAATs appear to have specialized roles at particular types of synapses. Dysfunction of EAATs is specifically implicated in the pathology of neurodegenerative conditions such as amyotrophic lateral sclerosis, epilepsy, Huntington's disease, Alzheimer's disease and ischemic stroke injury, and thus treatments that can modulate EAAT function may prove beneficial in these conditions. Recent advances have been made in our understanding of the regulation of EAATs, including their trafficking, splicing and post-translational modification. This article summarises some recent developments that improve our understanding of the roles and regulation of EAATs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Transport System X-AG / classification
  • Amino Acid Transport System X-AG / drug effects
  • Amino Acid Transport System X-AG / physiology*
  • Animals
  • Biological Transport
  • Humans

Substances

  • Amino Acid Transport System X-AG