Insulin secretion and protein phosphorylation in PKC-depleted islets of Langerhans

Life Sci. 1992;50(11):761-7. doi: 10.1016/0024-3205(92)90180-w.

Abstract

Protein kinase C (PKC)-dependent phosphorylation of endogenous substrates was measured in electrically permeabilised rat islets of Langerhans. The PKC-activating phorbol ester, 4 beta-phorbol myristate acetate (PMA), caused a slow but prolonged increase in insulin secretion from permeabilised islets, which was accompanied by increased 32P incorporation into several islet proteins of apparent M.W. 30-50 kDa. Depletion of islet PKC by prolonged exposure to PMA abolished subsequent secretory and phosphorylating responses to the phorbol ester. However, PKC-depleted islets did not show diminished responses to glucose, suggesting that PKC-mediated phosphorylation of these proteins is not essential for nutrient-induced insulin secretion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoradiography
  • Densitometry / methods
  • In Vitro Techniques
  • Insulin / metabolism*
  • Insulin Secretion
  • Islets of Langerhans / metabolism*
  • Permeability
  • Phosphorylation
  • Protein Kinase C / drug effects
  • Protein Kinase C / metabolism*
  • Proteins / metabolism*
  • Rats
  • Rats, Inbred Strains
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Insulin
  • Proteins
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate