TY - JOUR T1 - Enhanced Stimulatory Adenylyl Cyclase Signaling during Opioid Dependence Is Associated with a Reduction in Palmitoylated G<sub>sα</sub> JF - Molecular Pharmacology JO - Mol Pharmacol SP - 993 LP - 999 DO - 10.1124/mol.52.6.993 VL - 52 IS - 6 AU - Hermann Ammer AU - Rüdiger Schulz Y1 - 1997/12/01 UR - http://molpharm.aspetjournals.org/content/52/6/993.abstract N2 - Chronic opioid treatment of stably μ-opioid receptor transfected human mammary epidermoid A431 carcinoma cells (clone A431/μ13) results in sensitization of adenylyl cyclase (AC), a cellular adaptation associated with drug dependence. Up-regulation of AC is characterized by significantly increased levels of both basal and post-receptor-stimulated effector activities, which develop without any apparent change in the quantity of stimulatory G proteins and the maximum catalytic activity of AC. Here, we report that detergent extracts from membranes of chronically morphine-treated (10 μm; 2 days) A431/μ13 cells display higher stimulatory AC activities as assessed in the S49cyc −reconstitution assay. This finding is most likely due to an increased functional activity of Gsα because the addition of exogenous Gβγ subunits, which per sestimulate AC in S49cyc − membranes, failed to affect the difference in reconstitutive AC activity. Moreover, both chemical depalmitoylation by hydroxylamine and inhibition of palmitoyl-CoA transferase in vivo by tunicamycin treatment increased the reconstitutive activity of detergent extracts and eliminated the differences between native and opioid-dependent cells, indicating that the increase in stimulatory activity is due to depalmitoylation of Gsα. Indeed, metabolic labeling studies with [3H]palmitic acid revealed that chronic opioid treatment reduces considerably the fraction of palmitoylated Gsα in the plasma membrane. Furthermore, high affinity [3H]forskolin binding experiments demonstrated that depalmitoylated Gsα is able to associate directly with AC during the state of opioid dependence even without preceding receptor activation. These results suggest that post-translational palmitoylation of Gsα provides a potential regulator of transmembrane signaling. Moreover, accumulation of the depalmitoylated form of Gsα in the plasma membrane as reported herein may contribute to the increase in stimulatory AC signaling, as is characteristic for the state of opioid dependence. ER -