PKC modulation of GABAA receptor endocytosis and function is inhibited by mutation of a dileucine motif within the receptor β2 subunit

Dina Herring, Ren-Qi Huang, Meharvan Singh, Glenn H. Dillon, Nancy J. Leidenheimer

Research output: Contribution to journalArticleResearchpeer-review

47 Citations (Scopus)

Abstract

The modulation of GABAA receptors by protein kinase C is complex and involves effects on both ion channel function and receptor trafficking. Although PKC regulates receptor cell surface expression the mechanism is not well understood. Using immunofluorescence studies in HEK 293 cells, we demonstrate that activation of PKC by the phorbol ester PMA promotes receptor endocytosis and is dependent on the presence of a γ subunit. This endocytosis is blocked by the dominant negative dynamin mutant K44A indicating that PKC-induced receptor endocytosis involves the dynamin endocytic pathway. Mutation of a dileucine motif within the receptor β2 subunit inhibits the effect of PKC activation on receptor endocytosis. Using patch clamp analysis, we show that PKC activation produces a robust inhibition of GABA-gated chloride currents in cells expressing wildtype GABAA receptors, but it is ineffective in modulating receptors lacking the dileucine motif. Furthermore, the introduction into the patch pipette of a 10-amino acid peptide corresponding to the dileucine motif present in the receptor β2 subunit prevents PKC modulation of wildtype recombinant receptors. Furthermore, in cerebral cortical neuronal slices inclusion of this peptide in the patch pipette prevents PKC modulation of native GABAA receptors. Using limited chymotrypsin digestion assays, we also show that PKC increases receptor internalization in primary cultures of cerebral cortical neurons. Lastly, PKC inhibitors do not block constitutive receptor endocytosis or affect GABA-gated chloride currents suggesting that PKC-dependent phosphorylation is not required for GABA A receptor endocytosis but plays a modulatory role in the process.

Original languageEnglish
Pages (from-to)181-194
Number of pages14
JournalNeuropharmacology
Volume48
Issue number2
DOIs
StatePublished - 1 Jan 2005

Fingerprint

GABA-A Receptors
Endocytosis
Mutation
Dynamins
gamma-Aminobutyric Acid
Chlorides
Peptides
HEK293 Cells
Chymotrypsin
Cell Surface Receptors
Phorbol Esters
Ion Channels
Protein Kinase C
Fluorescent Antibody Technique
Digestion
Phosphorylation
Neurons
Amino Acids

Keywords

  • AP2 adaptin
  • Endocytosis
  • GABA receptor
  • Internalization
  • PKC
  • Phosphorylation

Cite this

Herring, Dina ; Huang, Ren-Qi ; Singh, Meharvan ; Dillon, Glenn H. ; Leidenheimer, Nancy J. / PKC modulation of GABAA receptor endocytosis and function is inhibited by mutation of a dileucine motif within the receptor β2 subunit. In: Neuropharmacology. 2005 ; Vol. 48, No. 2. pp. 181-194.
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PKC modulation of GABAA receptor endocytosis and function is inhibited by mutation of a dileucine motif within the receptor β2 subunit. / Herring, Dina; Huang, Ren-Qi; Singh, Meharvan; Dillon, Glenn H.; Leidenheimer, Nancy J.

In: Neuropharmacology, Vol. 48, No. 2, 01.01.2005, p. 181-194.

Research output: Contribution to journalArticleResearchpeer-review

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