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PMID: 203648 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Regulatory substances produced by lymphocytes. VI. Cell cycle specificity of inhibitor of DNA synthesis action in L cells.

The Journal of experimental medicine ·Vol. 147 ·No. 1 ·1978-01-01 ·Pages 171-81

Wagshal AB, Jegasothy BV, Waksman BH

Abstract

IDS inhibits DNA synthesis and mitosis of L cells only when present during the late G1 phase of the cell cycle, as shown with L cells synchronized by a variety of methods. This corresponds well with earlier findings that IDS inhibits DNA synthesis in mitogen-stimulated lymphocytes when present between 16 and 24 h after adding mitogen. In both cell types, the inhibition produced by IDS appears to be totally the result of elevation of cAMP level. Thus, inhibitors of cAMP phosphodiesterase work synergistically with IDS, and activators of cAMP phosphodiesterase overcome the inhibition by IDS. This paper shows that IDS raises cAMP levels in L cells only within a narrow interval of the cell cycle, around 6-8 h after mitosis. This cell cycle specificity, which may be related to appearance of receptors for IDS only at discrete times, may be important in limiting IDS action to suppression, as elevated cAMP levels have a variety of other effects during other phases of the cell cycle.

MeSH Terms
Animals Cyclic AMP/metabolism DNA/biosynthesis Glycoproteins/pharmacology Growth Inhibitors/pharmacology Imidazoles/pharmacology L Cells Lymphocytes/immunology Mitosis/drug effects Mitotic Index/drug effects Prostaglandins E/pharmacology Rats Xanthines/pharmacology
Chemicals
Glycoproteins Growth Inhibitors Imidazoles Prostaglandins E Xanthines DNA Cyclic AMP
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wagshal A B
Jegasothy B V
Waksman B H
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32 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1978-01-01
Pages
171-81
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2184092
Subset
IM
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