Transport activities and expression patterns of glycine transporters 1 and 2 in the developing murine brain stem and spinal cord

Biochem Biophys Res Commun. 2012 Jul 13;423(4):661-6. doi: 10.1016/j.bbrc.2012.06.007. Epub 2012 Jun 10.

Abstract

Glycine serves as a neurotransmitter in spinal cord and brain stem, where it activates inhibitory glycine receptors. In addition, it serves as an essential co-agonist of excitatory N-methyl-d-aspartate receptors. In the central nervous system, extracellular glycine concentrations are regulated by two specific glycine transporters (GlyTs), GlyT1 and GlyT2. Here, we determined the relative transport activities and protein levels of GlyT1 and GlyT2 in membrane preparations from mouse brain stem and spinal cord at different developmental stages. We report that early postnatally (up to postnatal day P5) GlyT1 is the predominant transporter isoform responsible for a major fraction of the GlyT-mediated [(3)H]glycine uptake. At later stages (≥ P10), however, the transport activity and expression of GlyT2 increases, and in membrane fractions from adult mice both GlyTs contribute about equally to glycine uptake. These alterations in the activities and expression profiles of the GlyTs suggest that the contributions of GlyT1 and GlyT2 to the regulation of extracellular glycine concentrations at glycinergic synapses changes during development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • Brain Stem / growth & development*
  • Brain Stem / metabolism
  • Glycine / metabolism*
  • Glycine Plasma Membrane Transport Proteins / antagonists & inhibitors
  • Glycine Plasma Membrane Transport Proteins / biosynthesis*
  • Glycine Plasma Membrane Transport Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Oocytes
  • Recombinant Proteins / antagonists & inhibitors
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / genetics
  • Sarcosine / analogs & derivatives
  • Sarcosine / pharmacology
  • Spinal Cord / growth & development*
  • Spinal Cord / metabolism
  • Xenopus laevis

Substances

  • (R)-(N-(3-(4'-fluorophenyl)-3-(4'-phenylphenoxy)propyl))sarcosine
  • Glycine Plasma Membrane Transport Proteins
  • Recombinant Proteins
  • Slc6a5 protein, mouse
  • Slc6a9 protein, mouse
  • Glycine
  • Sarcosine