RT Journal Article
SR Electronic
T1 Opioid Receptor Types Selectively Cointernalize with G Protein-Coupled Receptor Kinases 2 and 3
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 376
OP 384
DO 10.1124/jpet.300.2.376
VO 300
IS 2
A1 Rüdiger Schulz
A1 Andrea Wehmeyer
A1 Karin Schulz
YR 2002
UL http://jpet.aspetjournals.org/content/300/2/376.abstract
AB Activation of G protein-coupled receptors (GPCRs) may bring about their disappearance from the cell membrane, and it is commonly accepted that G protein-coupled receptor kinases (GRKs) play a key function in this mechanism. Opioid receptors belong to the family of GPCRs and are substrates of GRKs. We examined the fate of δ- and μ-opioid receptors and GRK2 and 3 in living cells during the process of receptor sequestration, using laser scanning microscopy. For visualization purposes, receptors and kinases were tagged at their respective C terminus with a fluorophore. The opioid receptors were fused to enhanced green fluorescence protein (EGFP), and the GRKs were linked to red fluorescence protein (DsRed). The cDNAs of these constructs served for transfection of human embryonic kidney 293 cells and neuroblastoma-glioma hybrid cells (NG 108-15), respectively. We report that activation of δ-opioid-EGFP receptors triggers a rapid translocation of cytosolic GRK-DsRed toward the cell membrane, which in turn releases vesicles carrying both green fluorescent δ-receptors and red fluorescent GRKs. Phosducin, a Gβγ scavenger, completely prevents translocation of GRKs and the formation of vesicles. In analogous experiments with μ-opioid receptors fused to EGFP, we observed that receptor activation also discharges green fluorescent vesicles. In contrast to δ-receptors, μ-receptors failed to trigger accumulation of GRK2 or 3 at the membrane, and no cointernalization of μ-opioid receptors with GRK2 or 3 was observed. The results suggest that δ-opioid receptors, but not μ-receptors, cointernalize with GRK2 or 3. The American Society for Pharmacology and Experimental Therapeutics