TY - JOUR
T1 - Correlation of increased levels of Ha‐ras T24 protein with extent of loss of gap junction function in rat liver epithelial cells
AU - de Feijter, Adriaan W.
AU - Trosko, James E.
AU - Krizman, David B.
AU - Lebovitz, Russell M.
AU - Lieberman, Michael W.
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1992
Y1 - 1992
N2 - 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 difference 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.
AB - 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 difference 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.
KW - Gap junction protein
KW - Intercellular communication
KW - Laser cytometry
KW - Oncogene expression
UR - http://www.scopus.com/inward/record.url?scp=0026506545&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0026506545&partnerID=8YFLogxK
U2 - 10.1002/mc.2940050307
DO - 10.1002/mc.2940050307
M3 - Article
C2 - 1375030
AN - SCOPUS:0026506545
VL - 5
SP - 205
EP - 212
JO - Molecular Carcinogenesis
JF - Molecular Carcinogenesis
SN - 0899-1987
IS - 3
ER -