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PMID: 7592612 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Hormone stimulation of type III adenylyl cyclase induces Ca2+ oscillations in HEK-293 cells.

The Journal of biological chemistry ·Vol. 270 ·No. 41 ·1995-10-13 ·Pages 24108-15

Wayman GA, Hinds TR, Storm DR

Abstract

Various forms of cross-talk between the Ca2+ and cAMP signal transduction systems can occur in animal cells depending upon the types of adenylyl cyclases present. Here, we report that Ca2+ oscillations can be generated by hormone stimulation of type III adenylyl cyclase expressed in HEK-293 cells. These Ca2+ oscillations are apparently due to the unique regulatory features of type III adenylyl cyclase, which is stimulated by hormones and inhibited by elevated Ca2+ in vivo. Ca2+ oscillations were generated by glucagon, isoproterenol, or forskolin stimulation of type III adenylyl cyclase and were dependent upon the activity of cAMP- and calmodulin-dependent protein kinases. Ca2+ oscillations were not solely dependent upon cAMP increases since dibutyryl cAMP or (Sp)-cAMP did not stimulate Ca2+ oscillations. We hypothesize that stimulation of type III adenylyl cyclase leads to increased cAMP, activation of inositol 1,4,5-trisphosphate receptors, and elevation of intracellular Ca2+. As free Ca2+ increases, type III adenylyl cyclase activity is attenuated by CaM kinase(s) and intracellular cAMP levels decrease. When cAMP levels drop below a threshold level, the inositol 1,4,5-trisphosphate receptor is dephosphorylated and Ca2+ is resequestered. This cycle is repeated if type III adenylyl cyclase is chronically exposed to an activator. This unique mechanism for generation of Ca2+ oscillations in cells is distinct from others documented in the literature.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives 1-Methyl-3-isobutylxanthine/pharmacology Adenylyl Cyclases/metabolism Calcium/metabolism Calcium Channels/metabolism Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors Carbachol/pharmacology Cell Line Colforsin/pharmacology Cyclic AMP/metabolism Enzyme Activation Enzyme Inhibitors/pharmacology Glucagon/pharmacology Humans Inositol 1,4,5-Trisphosphate Receptors Isoproterenol/pharmacology Isoquinolines/pharmacology Kidney Kinetics Models, Biological Oscillometry Phosphatidylinositols/metabolism Piperazines/pharmacology Receptors, Cytoplasmic and Nuclear/metabolism Receptors, Glucagon/drug effects,physiology Signal Transduction Time Factors
Chemicals
Calcium Channels Enzyme Inhibitors ITPR1 protein, human Inositol 1,4,5-Trisphosphate Receptors Isoquinolines Phosphatidylinositols Piperazines Receptors, Cytoplasmic and Nuclear Receptors, Glucagon Colforsin KN 62 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Carbachol Glucagon Cyclic AMP Calcium-Calmodulin-Dependent Protein Kinases Adenylyl Cyclases Isoproterenol Calcium 1-Methyl-3-isobutylxanthine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wayman G A
Department of Pharmacology, University of Washington, Seattle 98195, USA.
Hinds T R
Storm D R
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1995-10-13
Pages
24108-15
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL 44948 · United States
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