Microfilaments regulate the rate of exocytosis in rat basophilic leukemia cells

Biochem Biophys Res Commun. 1990 Aug 31;171(1):222-9. doi: 10.1016/0006-291x(90)91380-b.

Abstract

Disruption of microfilaments in rat basophilic leukemia (RBL) cells by exposure to cytochalasin B is observed to potentiate the rate of antigen-stimulated secretion from these cells. Under these conditions, cytochalasin B is without effect on the antigen-stimulated production of inositol phosphates or 45Ca2(+)-influx. In streptolysin-O-permeabilized RBL cells, cytochalasin B is observed to potentiate the rate of secretion in response both to guanosine 5'-(2-thio)-O-triphosphate (GTP gamma S) and to Ca2+ (buffered between 0.1 and 10 microM). However, under these conditions, cytochalasin B does not affect to antigen-stimulated production of inositol phosphates. Consistent with these data, microfilaments are proposed to regulate a terminal step in exocytosis, in a physiologically relevant manner.

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

  • Actin Cytoskeleton / physiology*
  • Actins / physiology*
  • Animals
  • Antigens
  • Basophils / physiology*
  • Calcium / physiology
  • Cytochalasin B / pharmacology
  • Cytoskeleton / physiology*
  • Exocytosis*
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Guanosine Triphosphate / analogs & derivatives
  • Guanosine Triphosphate / pharmacology
  • Inositol Phosphates / metabolism
  • Leukemia, Experimental
  • Rats
  • Serotonin / metabolism
  • Streptolysins / pharmacology
  • Thionucleotides / pharmacology
  • Tumor Cells, Cultured

Substances

  • Actins
  • Antigens
  • Inositol Phosphates
  • Streptolysins
  • Thionucleotides
  • Serotonin
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • Cytochalasin B
  • Guanosine Triphosphate
  • Calcium