Immunocytochemical expression and localization of protein kinase C in bovine aortic endothelial cells

Biochem Biophys Res Commun. 1992 Nov 30;189(1):40-6. doi: 10.1016/0006-291x(92)91522-r.

Abstract

Total PKC activity in BAEC incubated for 24 hrs in either 10% serum (FBS) or serum-deprived media (SDM) was similar. However, most of the activity (69%) in the FBS group was detected in the particulate fraction, while it was mainly in the cytosolic fraction (66%) in the SDM group. By confocal microscopy, there was diffuse cytoplasmic localization of the antibodies to the alpha and beta PKC isoforms. gamma PKC was not detected. Treatment of FBS or SDM cells with a phorbol ester resulted in an increase in PKC activity with translocation to the particulate fraction. PKC alpha immunofluorescence redistributed to the perinuclear region whereas PKC beta staining remained mostly cytosolic. Calphostin C, a PKC inhibitor, prevented the phorbol ester-induced increase in PKC activity and translocation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Aorta
  • Cattle
  • Cell Fractionation
  • Cell Membrane / enzymology
  • Cells, Cultured
  • Cytosol / enzymology
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / enzymology*
  • Fluorescent Antibody Technique
  • Immunohistochemistry / methods
  • Kinetics
  • Protein Kinase C / analysis
  • Protein Kinase C / isolation & purification
  • Protein Kinase C / metabolism*
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Protein Kinase C
  • Tetradecanoylphorbol Acetate