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PMID: 213832 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cellular interactions uncouple beta-adrenergic receptors from adenylate cyclase.

Science (New York, N.Y.) ·Vol. 202 ·No. 4369 ·1978-11-17 ·Pages 765-8

Ciment G, de Vellis J

Abstract

C6 glioma cells and B104 neuroblastoma cells both possess adenylate cyclase activity, but only C6 cells have beta-adrenergic receptors. However, when cocultured with B104 cells, C6 cells show a marked decrease in their ability to accumulate adenosine 3', 5'-monophosphate upon stimulation with beta receptor agonists. Since both beta receptors and cholera toxin-stimulated adenylate cyclase activities are present in C6/B104 cocultures, we conclude that the beta receptor/adenylate cyclase transduction mechanism in cocultured C6 cells is uncoupled.

MeSH Terms
Adenylyl Cyclases/metabolism Cell Communication Cell Line Cholera Toxin/pharmacology Cyclic AMP/metabolism Enzyme Activation/drug effects Membrane Proteins/metabolism Protein Binding Receptors, Adrenergic/metabolism Receptors, Adrenergic, beta/metabolism
Chemicals
Membrane Proteins Receptors, Adrenergic Receptors, Adrenergic, beta Cholera Toxin Cyclic AMP Adenylyl Cyclases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ciment G
de Vellis J
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1978-11-17
Pages
765-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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