Discordant and anomalous results among cytotoxicity assays: the confounding properties of eosinophil granule major basic protein on cell viability assays

J Immunol Methods. 1999 Jul 30;227(1-2):1-15. doi: 10.1016/s0022-1759(99)00055-1.

Abstract

When five cytotoxicity methods compared the toxicity of eosinophil granule major basic protein (MBP) and melittin to K562 and HL-60 cells, strikingly discrepant results were noted. Trypan blue staining, propidium iodide/CellTrackerGreen staining and incorporation of 14C-leucine assays indicated MBP damages > 75% of cells by 1 h. In contrast, 51Cr and lactic dehydrogenase (LDH) release assays indicated MBP damages most cells only at 20 h. All methods indicated melittin damages nearly all cells by 1 h. Further studies showed that without cell transfer, dye staining methods indicated MBP produces < 10% cytotoxicity after 4 h. A modified 14C-leucine assay, employing sodium dodecyl sulfate solubilization and trichloroacetic acid precipitation, showed lower cytotoxicity, 48%, at 4 h. Modified 51Cr and LDH assays showed increased cytotoxicities at 4 h, 34% and 58%, respectively. Overall, MBP's ability to cause molecular and cellular adhesion systematically confounds standard cytotoxicity measurements. However, the modified 14C-leucine assay provides a valid measure of MBP's cytotoxicity and may be useful for analyses of 'sticky' cytotoxins.

Publication types

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

MeSH terms

  • Blood Proteins / pharmacology*
  • Cell Adhesion
  • Cell Survival / drug effects
  • Cytotoxicity Tests, Immunologic / methods*
  • Dose-Response Relationship, Drug
  • Eosinophil Granule Proteins
  • Eosinophils / immunology*
  • Flow Cytometry
  • HL-60 Cells
  • Humans
  • K562 Cells
  • L-Lactate Dehydrogenase / metabolism
  • Leucine / metabolism
  • Melitten / pharmacology
  • Ribonucleases*

Substances

  • Blood Proteins
  • Eosinophil Granule Proteins
  • Melitten
  • L-Lactate Dehydrogenase
  • Ribonucleases
  • Leucine