Quantitation of binding and subcellular distribution of Clostridium perfringens enterotoxin in rat liver cells

Infect Immun. 1982 Aug;37(2):486-91. doi: 10.1128/iai.37.2.486-491.1982.

Abstract

Binding of enterotoxin from Clostridium perfringens type A was studied in suspensions of parenchymal and nonparenchymal cells from rat liver. In hepatocytes, 1.5 X 10(6) specific binding sites per cell with an association constant of 3.2 X 10(6) M-1 were found. About 1% of the added toxin was nonspecifically bound to the hepatocytes. At concentrations of toxin below 0.1 micrograms/ml, 80% of the toxin density of 7 X 10(6) cells per ml. Binding did not increase after the cells became permeable to the toxin. Subcellular fractionation in a sucrose gradient produced no evidence for binding to parts of the cell other than the plasma membrane. The degree of binding to nonparenchymal cells was less than 10% of the binding to hepatocytes.

MeSH terms

  • Animals
  • Binding Sites
  • Calcium / metabolism
  • Cell Survival
  • Clostridium Infections / metabolism
  • Clostridium Infections / mortality
  • Clostridium perfringens*
  • Egtazic Acid / pharmacology
  • Endothelium / cytology
  • Endothelium / metabolism
  • Enterotoxins / metabolism*
  • Kupffer Cells / metabolism
  • Liver / cytology
  • Liver / metabolism
  • Rats
  • Subcellular Fractions / analysis

Substances

  • Enterotoxins
  • Egtazic Acid
  • Calcium