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PMID: 2991919 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Potential role of the src gene product in inhibition of gap-junctional communication in NIH/3T3 cells.

Chang CC, Trosko JE, Kung HJ, Bombick D, Matsumura F

Abstract

The effects of the src gene on the activity of protein kinase C and intercellular communication have been studied in transformed NIH/3T3 clones isolated from soft agar following transfection with the plasmid carrying the v-src gene (psrc-11). Six transformed clones that were studied contained newly incorporated v-src genes in the genome, had an increased amount of pp60src, and showed enhanced activities of protein kinase C. Intercellular communication, studied by observing with autoradiography the transfer of [3H]uridine nucleotide from prelabeled donor cells to recipient cells in contact, was found to be reduced in transformed clones as compared to parental NIH/3T3 cells. Treatment with phorbol 12-myristate 13-acetate was also found to increase protein kinase C activity and to reduce intercellular communication in normal NIH/3T3 cells. These results suggest that the v-src gene product, in a manner similar to some of the powerful tumor promoters, may directly or indirectly affect cell-cell communication.

MeSH Terms
Animals Cell Communication Cell Transformation, Neoplastic Cells, Cultured Clone Cells DNA Restriction Enzymes Genes Intercellular Junctions/physiology Mice Mice, Inbred Strains Oncogene Protein pp60(v-src) Oncogenes Protein Kinase C Protein Kinases/genetics,metabolism Uracil Nucleotides/metabolism Viral Proteins/genetics,physiology
Chemicals
Uracil Nucleotides Viral Proteins Protein Kinases Oncogene Protein pp60(v-src) Protein Kinase C DNA Restriction Enzymes
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Chang C C
Trosko J E
Kung H J
Bombick D
Matsumura F
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38 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1985-08-00
Pages
5360-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC390568
Subset
IM
Grants
NCI NIH HHS · CA21104 · United States
NCI NIH HHS · CA33158 · United States
NIEHS NIH HHS · ESO-19631 · United States
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