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Pharmacological Distinction between Soluble and Transmembrane Adenylyl Cyclases

Authors :
Jacob L. Bitterman
Jochen Buck
Lonny R. Levin
Ana Diaz
Lavoisier Ramos-Espiritu
Source :
Journal of Pharmacology and Experimental Therapeutics. 347:589-598
Publication Year :
2013
Publisher :
American Society for Pharmacology & Experimental Therapeutics (ASPET), 2013.

Abstract

The second messenger cAMP is involved in a number of cellular signaling pathways. In mammals, cAMP is produced by either the hormonally responsive, G protein–regulated transmembrane adenylyl cyclases (tmACs) or by the bicarbonate- and calcium-regulated soluble adenylyl cyclase (sAC). To develop tools to differentiate tmAC and sAC signaling, we determined the specificity and potency of commercially available adenylyl cyclase inhibitors. In cellular systems, two inhibitors, KH7 and catechol estrogens, proved specific for sAC, and 2′,5′-dideoxyadenosine proved specific for tmACs. These tools provide a means to define the specific contributions of the different families of adenylyl cyclases in cells and tissues, which will further our understanding of cell signaling.

Details

ISSN :
15210103 and 00223565
Volume :
347
Database :
OpenAIRE
Journal :
Journal of Pharmacology and Experimental Therapeutics
Accession number :
edsair.doi.dedup.....e8291f50e59246d72a445c21cecff226
Full Text :
https://doi.org/10.1124/jpet.113.208496