Section 9
Chapter 8,673

Factors determining the specificity of signal transduction by guanine nucleotide-binding protein-coupled receptors. Integration of stimulatory and inhibitory input to the effector adenylyl cyclase

Marjamaki, A.; Sato, M.; Bouet-Alard, R.; Yang, Q.; Limon-Boulez, I.; Legrand, C.; Lanier, S.M.

Journal of Biological Chemistry 272(26): 16466-16473


ISSN/ISBN: 0021-9258
PMID: 9195955
DOI: 10.1074/jbc.272.26.16466
Accession: 008672976

Download citation:  

To define the integration of multiple signals by different types of adenylyl cyclase (AC) within the cell, we altered the population of enzymes expressed in the cell and determined the subsequent processing of stimulatory and inhibitory input. DDT-1-MF2 cells expressed AC VI-IX and were stably transfected with AC II, III, or IV. Enzyme expression was confirmed by RNA blot analysis and functional assays. Basal enzyme activity was only increased in AC II transfectants (6-fold). Maximum stimulation of enzyme activity was increased in each of the AC transfectants to varying extents. alpha-2A/D-AR activation elicited enzyme type-specific responses. alpha-2-AR activation inhibited the effect of isoproterenol in control transfectants, and this action was magnified in AC III transfectants. In AC II and AC IV transfectants, alpha-2-AR activation initiated both positive (G-beta-gamma) and negative signals (G-i-alpha) to the G-s-alpha-stimulated enzyme, and both types of signals were blocked by cell pretreatment with pertussis toxin. The negative input to AC II from the alpha-2-AR was blocked by protein kinase C activation in AC II transfectants, but it was the positive input to AC IV that was compromised by protein kinase C activation. These data indicate that the integration of multiple signals by adenylyl cyclases is a dynamic process depending upon the enzyme type and phosphorylation status.

PDF emailed within 0-6 h: $19.90