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1997: Kim S J; Chang Y Y; Kang S S; Chun J S
Phorbol ester effects in atypical protein kinase C zeta overexpressing NIH3T3 cells: possible evidence for crosstalk between protein kinase C isoforms.
Biochemical and biophysical research communications 1997;237(2):336-9.
To examine whether multiple protein kinase C (PKC) isoforms could interact or crosstalk, phorbol ester-insensitive atypical PKC (aPKC) zeta isoform was overexpressed in NIH3T3 cells, and the cells were stimulated with phorbol ester to activate diacylglycerol-dependent conventional (cPKC) and novel PKC (nPKC) isoforms. Treatment of cells with phorbol ester which activates PKCalpha, gamma, delta, and epsilon isoforms in NIH3T3 cells significantly reduced proliferation of cells. Overexpression of aPKCzeta and subsequent phorbol ester treatment abolished phorbol ester-induced reduction in cell proliferation. Overexpression of aPKCzeta also potentiated phorbol ester-induced mitogen-activated protein (MAP) kinase activation in a PKC-dependent manner. The effects of PKCzeta overexpression on proliferation and MAP kinase activation were proportional to the levels of aPKCzeta expression. Since aPKCzeta cannot be activated by phorbol ester, modulation of cell proliferation and MAP kinase activation by phorbol ester in aPKCzeta overexpressing cells might be due to the activation of cPKCs and/or nPKCs by phorbol ester. Thus, the results provide possible evidence for either direct or indirect crosstalk between PKC isoforms.

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