Pharmacological Distinction between Soluble and Transmembrane Adenylyl Cyclases

被引:83
作者
Bitterman, Jacob L. [1 ]
Ramos-Espiritu, Lavoisier [1 ]
Diaz, Ana [1 ]
Levin, Lonny R. [1 ]
Buck, Jochen [1 ]
机构
[1] Weill Cornell Med Coll, Dept Pharmacol, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
CYCLIC ADENINE RIBONUCLEOTIDE; NUCLEAR CAMP MICRODOMAIN; LONG-TERM POTENTIATION; P-SITE INHIBITION; PROTEIN-KINASE; NUCLEOSIDE; 3-POLYPHOSPHATES; DIFFERENT ISOFORMS; INDUCED ACTIVATION; TISSUE PARTICLES; MICE DEFICIENT;
D O I
10.1124/jpet.113.208496
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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.
引用
收藏
页码:589 / 598
页数:10
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