| Literature DB >> 1375030 |
A W de Feijter1, J E Trosko, D B Krizman, R M Lebovitz, M W Lieberman.
Abstract
Although it is known that cells transformed by ras and other oncogenes show reduced gap junction function, to date there has been no investigation of the quantitative relationship between intracellular levels of ras oncoprotein and loss of cell-cell communication. Using the rat liver epithelial cell line MTR6, which carries a zinc-inducible metallothionein ras T24 (MTrasT24) fusion gene, we showed a direct correlation between the accumulation of ras T24 protein and the loss of dye transfer as measured by interactive laser cytometry. After stimulation with zinc sulfate, changes in both parameters were rapid and measurable by 24 h. Similarly, there was a dose-response relationship between loss of gap junction function and increase in ras T24 protein. Northern analysis of two gap junction proteins (connexins 43 and 32) showed no differences between cells that expressed high levels of ras and control cells. These data demonstrate that the degree of loss of gap junction function is dependent on the amount of increase in ras T24 protein levels, but the mechanism by which these changes are effected remains unclear.Entities:
Mesh:
Substances:
Year: 1992 PMID: 1375030 DOI: 10.1002/mc.2940050307
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784