Embryonic rat spinal cord neurons change expression of glycine receptor subtypes during development in vitro

J Neurobiol. 1997 Jun 5;32(6):579-92. doi: 10.1002/(sici)1097-4695(19970605)32:6<579::aid-neu4>3.0.co;2-x.

Abstract

The expression of functional glycine receptors (GlyRs) by embryonic rat spinal cord neurons during development in vitro was investigated using whole-cell patch-clamp recordings. Functional GlyRs were expressed by most neurons within 1 day in vitro, and by all neurons from 4 days onward. However, the extent to which responses to glycine were blocked by the antagonist strychnine differed significantly between the first few days and 8 days in culture. Responses to glycine by neurons during the first few days in culture exhibited significantly less blockade by strychnine than those in neurons after 1 week in culture. Responses to glycine at both ages reflected an increased conductance to chloride ions, ruling out involvement of N-methyl-D-aspartate type glutamate receptors, and were not due to cross activation of gamma-aminobutyric acid receptors. Monoclonal antibody 4a, which recognizes multiple subtypes of rat GlyR alpha subunits, labeled most neurons as early as 1 day in vitro, confirming that neurons express some form of GlyR alpha subunits by the first day in culture. These results show that rat spinal cord neurons express GlyRs early in their differentiation in vitro, and they suggest that individual neurons express as functional, cell-surface GlyRs a strychnine-insensitive isoform of the GlyR, possibly the previously described alpha 2* subunit. In addition, these results indicate that the expression of GlyR isoforms changes from predominantly a strychnine-insensitive isoform to other, strychnine-sensitive isoform(s) GlyR during development in vitro.

Publication types

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

MeSH terms

  • Animals
  • Cells, Cultured
  • Cellular Senescence
  • Embryo, Mammalian
  • Glycine / pharmacology*
  • Membrane Potentials / drug effects
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA / physiology
  • Receptors, Glycine / biosynthesis*
  • Receptors, Glycine / physiology
  • Spinal Cord / embryology
  • Spinal Cord / physiology*
  • Strychnine / pharmacology
  • Time Factors

Substances

  • Receptors, GABA
  • Receptors, Glycine
  • Strychnine
  • Glycine