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PMID: 6296654 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Differences in the forskolin activation of adenylate cyclases in wild-type and variant lymphoma cells.

Molecular pharmacology ·Vol. 22 ·No. 3 ·1982-11-00 ·Pages 609-13

Clark RB, Goka TJ, Green DA, Barber R, Butcher RW

Abstract

The ability of the diterpene forskolin to stimulate cyclic AMP accumulation in intact cell and membrane preparations of wild-type S49 lymphoma cells (WT) and a number of variants has been confirmed. Additionally, a number of salient new findings have emerged: (a) A time delay in forskolin stimulation of cyclic AMP accumulation and adenylate cyclase (t 1/2 approximately equal to 1.5 min) occurred in all hormone-sensitive WT and variant cell and membrane preparations tested. (b) The time delay was missing in the adenylate cyclase-deficient variant (cyc-) of the S49 lymphoma cell, which also lacks functional adenylate cyclase-coupling proteins. (c) The simultaneous addition of epinephrine and forskolin to WT cells or to membrane preparations eliminated the time delay. (d) Forskolin stimulation of intact WT cells did not appear to desensitize adenylate cyclase. (e) The activation of WT adenylate cyclase by forskolin was biphasic with respect to concentration, with both high- and low-affinity components being apparent. In cyc-, only the low-affinity component was detected.

MeSH Terms
Adenylyl Cyclases/metabolism Animals Cell Membrane/metabolism Cells, Cultured Colforsin Cyclic AMP/metabolism Diterpenes/pharmacology Enzyme Activation/drug effects Epinephrine/pharmacology Lymphoma/metabolism Neoplasms, Experimental/metabolism Time Factors
Chemicals
Diterpenes Colforsin Cyclic AMP Adenylyl Cyclases Epinephrine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Clark R B
Goka T J
Green D A
Barber R
Butcher R W
Article Info
Journal
Molecular pharmacology
Abbr.
Mol Pharmacol
ISSN
0026-895X
Published
1982-11-00
Pages
609-13
Language
English
Region
United States
NLM ID
0035623
Subset
IM
Grants
NIADDK NIH HHS · AM 26943-03 · United States
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