TY - JOUR
T1 - Nontransformed cells can normalize gap junctional communication with transformed cells
AU - Valiunas, Virginijus
AU - Bechberger, John F.
AU - Naus, Christian C.G.
AU - Brink, Peter R.
AU - Goldberg, Gary S.
N1 - Funding Information:
This work was supported by grants from the United States National Institutes of Health CA88805 and EY014479 to G.S.G. and GM555263 to P.R.B., the Canadian Institutes of Health Research MOP-14358 to C.C.N., and the American Heart Association AHA0335236N to V.V.
PY - 2005/7/22
Y1 - 2005/7/22
N2 - We demonstrate that the Src kinase can augment gap junctional communication between cells derived from homozygous null Cx43 knockout mice. The total conductance between Src transformed cells was nearly twice that of nontransformed cells. In addition, the unitary conductance of the majority of single channel events between transformed cells was about 35% greater than that of nontransformed cells. Analysis showed that both nontransformed and transformed cells expressed at least two populations of channels, suggesting that Src increased junctional conductance by up-regulating one population and/or by increasing the unitary conductance of another population of channels. Interestingly, the conductance displayed by heterologous pairs of transformed and nontransformed cells resembled that of nontransformed cells. The majority of single channel events between heterologous pairs shifted back to lower conductances that were exhibited by nontransformed cells. Thus, nontransformed cells can effectively "normalize" the conductance of gap junction channels expressed by adjacent tumor cells.
AB - We demonstrate that the Src kinase can augment gap junctional communication between cells derived from homozygous null Cx43 knockout mice. The total conductance between Src transformed cells was nearly twice that of nontransformed cells. In addition, the unitary conductance of the majority of single channel events between transformed cells was about 35% greater than that of nontransformed cells. Analysis showed that both nontransformed and transformed cells expressed at least two populations of channels, suggesting that Src increased junctional conductance by up-regulating one population and/or by increasing the unitary conductance of another population of channels. Interestingly, the conductance displayed by heterologous pairs of transformed and nontransformed cells resembled that of nontransformed cells. The majority of single channel events between heterologous pairs shifted back to lower conductances that were exhibited by nontransformed cells. Thus, nontransformed cells can effectively "normalize" the conductance of gap junction channels expressed by adjacent tumor cells.
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U2 - 10.1016/j.bbrc.2005.05.104
DO - 10.1016/j.bbrc.2005.05.104
M3 - Article
C2 - 15936725
AN - SCOPUS:20444465195
SN - 0006-291X
VL - 333
SP - 174
EP - 179
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -