Premium
Effect of G Protein‐Coupled Receptor Kinase 2 on the Sensitivity of M4 Muscarinic Acetylcholine Receptors to Agonist‐Induced Internalization and Desensitization in NG108‐15 Cells
Author(s) -
Holroyd E. W.,
Szekeres P. G.,
Whittaker R. D.,
Kelly E.,
Edwardson J. M.
Publication year - 1999
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1999.0731236.x
Subject(s) - internalization , homologous desensitization , carbachol , muscarinic acetylcholine receptor , muscarinic acetylcholine receptor m3 , agonist , muscarinic acetylcholine receptor m5 , muscarinic acetylcholine receptor m2 , receptor , chemistry , endocrinology , endocytosis , g protein coupled receptor kinase , muscarinic acetylcholine receptor m1 , desensitization (medicine) , medicine , microbiology and biotechnology , biology , stimulation , g protein , biochemistry
: NG108‐15 cells express predominantly the M4 subtype of the muscarinic receptor for acetylcholine. Stimulation of these receptors by the agonist carbachol causes an inhibition of cellular adenylyl cyclase and a consequent fall in the intracellular cyclic AMP concentration. Pretreatment of the cells with carbachol caused both internalization and desensitization of the M4 receptor. Overexpression of G protein‐coupled receptor kinase (GRK) 2 caused an increase in the rate constant for receptor endocytosis (from 0.06 to 0.18 min ‐1 ) and a decrease in the EC 50 for carbachol stimulation of internalization (from 15 to 3 μ M ). Overexpression of a dominant negative form of GRK2 had more modest effects, reducing the rate constant for endocytosis (from 0.11 to 0.07 min ‐1 ) and increasing the EC 50 for carbachol stimulation of internalization (from 8 to 17 μ M ). Neither GRK2 nor dominant negative GRK2 overexpression had any effect on the rate constant for receptor recycling following agonist removal. The time course and extent of receptor desensitization in control cells were identical to the corresponding values for receptor internalization, and the rate and extent of desensitization were again increased by GRK2 overexpression. Exposure of the cells to hyperosmolar sucrose (0.6 M ) almost completely blocked agonist‐induced receptor internalization in both control and GRK2‐overexpressing cells. Sucrose treatment also blocked agonist‐induced desensitization. We conclude that the internalization and desensitization of the M4 muscarinic receptor in NG108‐15 cells can be modulated in response to changes in GRK2 activity and also that internalization plays a key role in desensitization.