RBL-2H3 cells are an imprecise model for mast cell mediator release

Inflamm Res. 2009 Sep;58(9):611-8. doi: 10.1007/s00011-009-0028-4. Epub 2009 Mar 20.

Abstract

Objective: The cell line, RBL-2H3, has been widely used as a mast cell model though much of the data is contradictory. The aim of this study is to assess the RBL-2H3 cell line as an in vitro model for degranulation studies.

Methods: RBL-2H3 cells were stimulated with either dinitrophenylated-IgE, calcium ionophore A23187, compound 48/80, mast cell degranulating peptide or lipopolysaccharide and mediator (histamine, beta-hexosaminidase, interleukin-13 and TNF-alpha) release was analysed. Toll-like receptors (TLR) mRNA expression in RBL-2H3 cells and rat peritoneal mast cells (RPMC) were compared by RT-PCR. TLR4 and CD14 surface proteins in RBL-2H3 were analysed by FACS.

Results: Mediator release was dependent on media composition and degranulation was stimulated by IgE and A23187. Degranulation was inhibited by quercetin, but not by cromoglycate or ketotifen. Transcripts encoding TLR3-5 and 6 were detected in RBL-2H3 cells whereas TLR1-6 and TLR8 were clearly seen in RPMC. While proteins were detected for TLR4 in RBL-2H3 cells, CD14 was largely absent.

Conclusions: While RBL-2H3 cells may be useful as a model for mast cell IgE-mediated degranulation, other aspects may not be representative and they may share similarities with basophils rather than with other histamine-releasing cell types.

MeSH terms

  • Animals
  • Calcimycin / pharmacology
  • Cell Degranulation / immunology*
  • Cell Line*
  • Cytokines / immunology
  • Immunoglobulin E / immunology
  • Interleukin-13 / immunology
  • Ionophores / pharmacology
  • Lipopolysaccharide Receptors / immunology
  • Lipopolysaccharides / immunology
  • Lipopolysaccharides / pharmacology
  • Mast Cells / cytology
  • Mast Cells / drug effects
  • Mast Cells / immunology*
  • Rats
  • Toll-Like Receptors / immunology
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Cytokines
  • Interleukin-13
  • Ionophores
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha
  • Immunoglobulin E
  • Calcimycin