Characterization of a Rana catesbeiana lectin-resistant mutant of leukemia P388 cells

Cancer Res. 1994 Feb 15;54(4):928-34.

Abstract

Sialic acid-binding lectin (SBL-C) from Rana catesbeiana eggs inhibits the growth of tumor cells such as P388 and L1210 leukemia cells (K. Nitta et al., Cancer Res., 54: 920-927, 1994). Here we report the establishment of an SBL-resistant P388 variant cell line, RC-150. Both P388 and RC-150 cells were agglutinated by SBL-C; however, growth of RC-150 cells was unaffected by SBL-C. Cytoplasmic free Ca2+ concentration and transglutaminase activity of RC-150 cells were 0.5 (110 nM) and 3 times (0.62 nmol/mg/min) as high as those of P388 cells, respectively. Microvilli and microplicae were observed on the surface of P388 cells by scanning electron microscopy but were rarely seen on RC-150 cells. Dansylcadaverine-labeled SBL-C bound to both P388 and RC-150 cells. Binding of SBL-C to these tumor cells appears to be mediated by two species of wheat germ agglutinin-stained cell membrane sialoglycoproteins. Labeled SBL-C entered P388 but not RC-150 cells, suggesting that internalized SBL-C acts as an inhibitor of cell proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agglutination
  • Amino Acid Sequence
  • Animals
  • Calcium / metabolism
  • Drug Resistance
  • Lectins / metabolism
  • Lectins / pharmacology*
  • Leukemia P388 / pathology*
  • Membrane Glycoproteins / analysis
  • Mice
  • Molecular Sequence Data
  • Mutation
  • N-Acetylneuraminic Acid
  • Neuraminidase / pharmacology
  • Rana catesbeiana*
  • Sialic Acid Binding Immunoglobulin-like Lectins
  • Sialic Acids / analysis

Substances

  • Lectins
  • Membrane Glycoproteins
  • Sialic Acid Binding Immunoglobulin-like Lectins
  • Sialic Acids
  • Neuraminidase
  • N-Acetylneuraminic Acid
  • Calcium