Abstract
Cultured mouse lymphosarcoma cells are killed on exposure to 0.1 mM N(6),O(2')-dibutyryl-adenosine 3':5'-cyclic monophosphate. A population of cells resistant to the killing effect of dibutyryl cyclic AMP at concentrations as high as 1 mM was selected. The growth characteristics of the resistant cells were similar to those of the sensitive parental line. However, the resistant cells contain less cytoplasmic cyclic AMP-binding proteins and decreased cyclic AMP-stimulated protein kinase activity. It is proposed that transition from sensitivity to resistance to dibutyryl cyclic AMP in lymphoma cells is connected with a modification of the cyclic AMP-binding protein, which appears to be the regulatory subunit of the cyclic AMP-activated protein kinase.
MeSH Terms
Animals
Cell Division/drug effects
Cell Line
Cell Survival/drug effects
Cell-Free System
Cells, Cultured
Chromatography, Ion Exchange
Cyclic AMP/metabolism,pharmacology
Enzyme Activation/drug effects
Hydrogen-Ion Concentration
Lymphoma/enzymology
Mice
Neoplasm Proteins/isolation & purification,metabolism
Phosphotransferases/isolation & purification,metabolism
Protein Binding
Receptors, Drug
Tritium
Chemicals
Neoplasm Proteins
Receptors, Drug
Tritium
Cyclic AMP
Phosphotransferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Daniel V
Litwack G
Tomkins G M
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12 references, click to expand
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