9282934

pubmed:Citation

3

Both the Ca2+/phospholipid-dependent protein kinases (protein kinases C, PKCs) and mitogen-activated protein kinases (MAPKs) have been implicated as participants in the secretory response of bovine adrenomedullary chromaffin cells. To investigate a possible role for these kinases in exocytosis and the relationship of these kinases to one another, intact chromaffin cells were treated with agents that inhibited each of the kinases and analyzed for catecholamine release and MAPK/extracellular signal-regulated kinase (ERK) kinase (MEK)/MAPK activation after stimulation with secretagogues of differential efficacy. Of the three secretagogues tested, inactivation of PKCs by long-term phorbol 12-myristate 13-acetate (PMA) treatment or incubation with GF109203X had the greatest inhibitory effect on nicotine-induced catecholamine release and MEK/MAPK activation, a moderate effect on KCl-induced events, and little, if any, effect on Ca2+ ionophore-elicited exocytosis and MEK/MAPK activation. These results indicate that PKC plays a significant role in events induced by the optimal secretagogue nicotine and a lesser role in exocytosis elicited by the suboptimal secretagogues KCl and Ca2+ ionophore. Treatment of cells with the MEK-activation inhibitor PD098059 completely inhibited MEK/MAPK activation (IC50 1-5 microM) and partially inhibited catecholamine release induced by all secretagogues. However, PD098059 was more effective at inhibiting exocytosis induced by suboptimal secretagogues (IC50 approximately 10 microM) than that induced by nicotine (IC50 approximately 30 microM). These results suggest a more prominent role for MEK/MAPK in basic secretory events activated by suboptimal secretagogues than in those activated by the optimal secretagogue nicotine. However, PD098059 also partially blocked secretion potentiated by short-term PMA treatment, suggesting that PKC can function in part by signaling through MEK/MAPK to enhance secretion. Taken together, these results provide evidence for the preferential involvement of MEK/MAPK in basic secretory events activated by the suboptimal secretagogues KCl and Ca2+ ionophore and the participation of both PKC and MEK/MAPK in optimal, secretion induced by nicotine.

eng

IM

MEDLINE

0022-3042

Print

NLM

1119-30

pubmed-meshheading:9282934-Adrenal Medulla, pubmed-meshheading:9282934-Animals, pubmed-meshheading:9282934-Calcimycin, pubmed-meshheading:9282934-Calcium-Calmodulin-Dependent Protein Kinases, pubmed-meshheading:9282934-Cattle, pubmed-meshheading:9282934-Cells, Cultured, pubmed-meshheading:9282934-Chromaffin Cells, pubmed-meshheading:9282934-Enzyme Activation, pubmed-meshheading:9282934-Enzyme Inhibitors, pubmed-meshheading:9282934-Exocytosis, pubmed-meshheading:9282934-Flavonoids, pubmed-meshheading:9282934-Indoles, pubmed-meshheading:9282934-Kinetics, pubmed-meshheading:9282934-Maleimides, pubmed-meshheading:9282934-Nicotine, pubmed-meshheading:9282934-Norepinephrine, pubmed-meshheading:9282934-Potassium Chloride, pubmed-meshheading:9282934-Protein Kinase C, pubmed-meshheading:9282934-Signal Transduction, pubmed-meshheading:9282934-Tetradecanoylphorbol Acetate

Roles for protein kinase C and mitogen-activated protein kinase in nicotine-induced secretion from bovine adrenal chromaffin cells.

Journal Article, Research Support, U.S. Gov't, P.H.S.