Inhibition of histamine release from RBL-2H3 cells by protein synthesis inhibitors

Int Arch Allergy Immunol. 1994;103(3):266-73. doi: 10.1159/000236638.

Abstract

Effects of cycloheximide, an inhibitor of protein synthesis, on histamine release from RBL-2H3 cells were examined. RBL-2H3 cells sensitized by rat antiserum to ascaris extract were challenged by the antigen, and histamine release during a period of 30 min was measured. Pretreatment with cycloheximide (1 microgram/ml) for 1 h significantly inhibited the antigen-induced histamine release (36% inhibition). The cycloheximide-induced inhibition of histamine release was abolished when the cells were further incubated in the absence of cycloheximide for 2 h. Pretreatment with puromycin (3 and 10 micrograms/ml), an inhibitor of protein synthesis, or actinomycin D (0.1-1 microgram/ml), an inhibitor of DNA-dependent RNA synthesis, also inhibited the antigen-induced histamine release in a concentration-dependent manner. Both ionomycin- and thapsigargin-induced histamine release were also inhibited by pretreatment with cycloheximide. Measurement of intracellular Ca2+ levels using quin 2 revealed that cycloheximide inhibits the increase in Ca2+ levels induced by the antigen, ionomycin or thapsigargin. These results suggest that histamine release induced by the antigen, ionomycin and thapsigargin in RBL-2H3 cells is mediated by protein(s) which is newly synthesized and inactivated rapidly, and the newly synthesized protein(s) is involved in the increase of intracellular Ca2+ levels induced by these stimulants.

MeSH terms

  • Animals
  • Antigens / pharmacology
  • Calcium / analysis
  • Carcinogens / pharmacology
  • Culture Media, Conditioned / chemistry
  • Cycloheximide / pharmacology*
  • Dactinomycin / pharmacology
  • Histamine Release / drug effects*
  • Histamine Release / immunology
  • Ionomycin / pharmacology
  • Leukemia, Basophilic, Acute
  • Protein Biosynthesis
  • Proteins / antagonists & inhibitors
  • Puromycin / pharmacology
  • Rats
  • Terpenes / pharmacology
  • Thapsigargin
  • Tumor Cells, Cultured / metabolism

Substances

  • Antigens
  • Carcinogens
  • Culture Media, Conditioned
  • Proteins
  • Terpenes
  • Dactinomycin
  • Puromycin
  • Ionomycin
  • Thapsigargin
  • Cycloheximide
  • Calcium