Requirement for metalloendoprotease in exocytosis: evidence in mast cells and adrenal chromaffin cells

Cell. 1985 Mar;40(3):645-56. doi: 10.1016/0092-8674(85)90213-2.

Abstract

Exocytosis is initiated by the receptor-mediated influx of calcium that results in fusion of the secretory vesicle with the plasma membrane. We examined the possibility that calcium-dependent exocytosis in mast cells and adrenal chromaffin cells requires metalloendoprotease activity. Metalloendoprotease inhibitors and dipeptide substrates block exocytosis in these cells with the same specificity and dose dependency as that with which they interact with metalloendoproteases. Metalloendoprotease activity is identified in these cells with fluorogenic synthetic substrates, which also blocked exocytosis. Metalloendoprotease activity is highest in the plasma membrane of chromaffin cells. The metalloendoprotease appears to be required in exocytosis at a step dependent on or after calcium entry, since exocytosis initiated by direct calcium introduction in both mast cells and chromaffin cells is blocked by metalloendoprotease inhibitors.

Publication types

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

MeSH terms

  • Adrenal Glands / cytology*
  • Animals
  • Calcimycin / pharmacology
  • Calcium / metabolism
  • Calcium / pharmacology
  • Cattle
  • Cell Membrane / enzymology
  • Chromaffin System / cytology*
  • Concanavalin A / pharmacology
  • Dipeptides / pharmacology
  • Endopeptidases / physiology*
  • Exocytosis* / drug effects
  • Female
  • Histamine Release / drug effects
  • Mast Cells / physiology*
  • Metalloendopeptidases
  • Oligopeptides / metabolism
  • Phenanthrolines / pharmacology
  • Protease Inhibitors / pharmacology
  • Rats
  • Rats, Inbred Strains

Substances

  • Dipeptides
  • Oligopeptides
  • Phenanthrolines
  • Protease Inhibitors
  • 2-aminobenzoylalanyl-glycyl-leucyl-alanyl-4-nitrobenzylamide
  • Concanavalin A
  • Calcimycin
  • Endopeptidases
  • Metalloendopeptidases
  • Calcium
  • 1,10-phenanthroline