Related Experiment Videos
Antagonistic effects of protein kinase C alpha and delta on both transformation and phospholipase D activity mediated
1Department of Biological Sciences, Hunter College of The City University of New York, New York, New York 10021, USA.
Abstract:
Downregulation of protein kinase C delta (PKC delta) by treatment with the tumor-promoting phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA) transforms cells that overexpress the non-receptor class tyrosine kinase c-Src (Z. Lu et al., Mol. Cell. Biol. 17:3418-3428, 1997). We extended these studies to cells overexpressing a receptor class tyrosine kinase, the epidermal growth factor (EGF) receptor (EGFR cells); like c-Src, the EGF receptor is overexpressed in several human tumors. In contrast with expectations, downregulation of PKC isoforms with TPA did not transform the EGFR cells; however, treatment with EGF did transform these cells. Since TPA downregulates all phorbol ester-responsive PKC isoforms, we examined the effects of PKC delta- and PKC alpha-specific inhibitors and the expression of dominant negative mutants for both PKC delta and alpha. Consistent with a tumor-suppressing function for PKC delta, the PKC delta-specific inhibitor rottlerin and a dominant negative PKC delta mutant transformed the EGFR cells in the absence of EGF. In contrast, the PKC alpha-specific inhibitor Go6976 and expression of a dominant negative PKC alpha mutant blocked the transformed phenotype induced by both EGF and PKC delta inhibition. Interestingly, both rottlerin and EGF induced substantial increases in phospholipase D (PLD) activity, which is commonly elevated in response to mitogenic stimuli. The elevation of PLD activity in response to inhibiting PKC delta, like transformation, was dependent upon PKC alpha and restricted to the EGFR cells. These data demonstrate that PKC isoforms alpha and delta have antagonistic effects on both transformation and PLD activity and further support a tumor suppressor role for PKC delta that may be mediated by suppression of tyrosine kinase-dependent increases in PLD activity.
Insights
Protein Kinase C delta (PKC delta) acts as a tumor suppressor by inhibiting phospholipase D (PLD) activity. Inhibition of PKC delta promotes cell transformation, while PKC alpha promotes it, revealing their antagonistic roles.
Area of Science:
- Molecular Biology
- Cell Biology
- Oncology
Background:
- Protein Kinase C delta (PKC delta) downregulation by 12-O-tetradecanoylphorbol-13-acetate (TPA) transforms cells overexpressing c-Src.
- Epidermal Growth Factor (EGF) receptor (EGFR) is overexpressed in human tumors.
- The role of PKC isoforms in EGFR-overexpressing cells was unexplored.
Purpose of the Study:
- To investigate the role of PKC isoforms in the transformation of EGFR-overexpressing cells.
- To determine the specific functions of PKC delta and PKC alpha in cell transformation and phospholipase D (PLD) activity.
- To elucidate the antagonistic relationship between PKC delta and PKC alpha.
Main Methods:
- Treatment of EGFR-overexpressing cells with TPA, EGF, PKC delta-specific inhibitor (rottlerin), and PKC alpha-specific inhibitor (Go6976).
- Expression of dominant-negative mutants for PKC delta and PKC alpha.
- Assay of phospholipase D (PLD) activity.
- Assessment of cell transformation phenotype.
Main Results:
- TPA treatment did not transform EGFR cells, but EGF treatment did.
- PKC delta inhibition (rottlerin or dominant-negative mutant) transformed EGFR cells independently of EGF, suggesting a tumor-suppressing role for PKC delta.
- PKC alpha inhibition (Go6976 or dominant-negative mutant) blocked EGF- and PKC delta inhibition-induced transformation.
- Both rottlerin and EGF increased PLD activity; this increase was dependent on PKC alpha and EGFR cells.
- PKC delta suppressed tyrosine kinase-dependent increases in PLD activity.
Conclusions:
- PKC delta and PKC alpha exhibit antagonistic effects on cell transformation and PLD activity.
- PKC delta functions as a tumor suppressor in EGFR-overexpressing cells.
- PKC delta may exert its tumor-suppressive function by inhibiting tyrosine kinase-mediated PLD activation.