Abstract
When the four Torpedo acetylcholine receptor (AcChoR) subunit cDNAs are stably integrated into the genome of mouse fibroblast cells, alpha 2 beta gamma delta pentamers with proper pharmacological and electrophysiological properties are expressed on the cell surface. Expression of these AcChoRs can be regulated by agents that stimulate intracellular cAMP levels with the result that increased numbers of cell-surface AcChoRs are produced. Theophylline, 8-(4-chlorophenylthio)-adenosine 3':5'-cyclic monophosphate, cholera toxin, and forskolin stimulated AcChoR cell-surface expression 1.2-, 1.6-, 2.2-, and 2.3-fold, respectively. cAMP-stimulated expression is mediated through a posttranslational mechanism, and the observed increase in surface AcChoRs correlates with increased lifetimes of each newly synthesized subunit. Increased subunit lifetimes are not observed in cell lines expressing each subunit individually, indicating that subunit stabilization arises through heterologous subunit-subunit interactions.
MeSH Terms
Animals
Bungarotoxins/metabolism
Cell Line
Cell Membrane/metabolism
Cholera Toxin/pharmacology
Colforsin/pharmacology
Cyclic AMP/analogs & derivatives,pharmacology,physiology
Cycloheximide/pharmacology
DNA/genetics
Kinetics
L Cells/metabolism
Macromolecular Substances
Mice
Protein Processing, Post-Translational/drug effects
Receptors, Cholinergic/drug effects,genetics
Theophylline/pharmacology
Thionucleotides/pharmacology
Torpedo
Transfection
Chemicals
Bungarotoxins
Macromolecular Substances
Receptors, Cholinergic
Thionucleotides
Colforsin
8-((4-chlorophenyl)thio)cyclic-3',5'-AMP
DNA
Cholera Toxin
Cycloheximide
Theophylline
Cyclic AMP
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Green W N
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06510.
Ross A F
Claudio T
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