Differential internalisation of mGluR1 splice variants in response to agonist and phorbol esters in permanently transfected BHK cells

FEBS Lett. 1997 Nov 24;418(1-2):83-6. doi: 10.1016/s0014-5793(97)01353-7.

Abstract

The internalisation of metabotropic glutamate receptor (mGluR1alpha) and its splice variant (mGluR1beta), in response to agonist and phorbol esters (PMA), has been studied. Both mGluR1alpha and mGluR1beta exhibit a similar rate of internalisation following PMA treatment, with a shift in their distribution from plasma membrane to endosome-enriched membrane fractions. Agonist challenge however caused a rapid loss, within 5-10 min, of mGluR1beta but not mGluR1alpha from the cell surface. These results show that the two forms of mGluR1 show different internalisation responses to agonist and suggest that the C-terminal region of the molecule plays an important role in this phenomenon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Animals
  • Cell Line
  • Cell Membrane / metabolism
  • Cricetinae
  • Endosomes / metabolism
  • Genetic Variation*
  • Kidney
  • Kinetics
  • Receptors, Metabotropic Glutamate / biosynthesis*
  • Receptors, Metabotropic Glutamate / metabolism
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / metabolism
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transfection

Substances

  • Receptors, Metabotropic Glutamate
  • Recombinant Fusion Proteins
  • metabotropic glutamate receptor type 1
  • Tetradecanoylphorbol Acetate