Acidic environment augments FcεRI-mediated production of IL-6 and IL-13 in mast cells

Biochem Biophys Res Commun. 2015 Aug 28;464(3):949-55. doi: 10.1016/j.bbrc.2015.07.077. Epub 2015 Jul 18.

Abstract

Although blood pH is maintained in a narrow range of around pH 7.4 in living organisms, inflammatory loci are characterized by acidic conditions. Mast cells tend to reside close to the surface of the body in areas such as the mucosa and skin where they may be exposed to exogenous acids, and they play an important role in immune responses. However, little is known about the effects of extracellular acidification on the functions of mast cell. Here, we found that extracellular acidification increased the dinitrophenyl-conjugated human serum albumin (DNP-HSA)-induced production of interleukin (IL)-6 and IL-13 in MC/9 cells or bone marrow-derived mouse mast cells sensitized with anti-DNP IgE. Extracellular acidification also inhibited migration of MC/9 cells toward DNP-HSA. In addition, acidic pH stimulated antigen-induced activation of p38 mitogen-activated protein kinase (MAPK) and protein kinase B (Akt). These findings suggest that extracellular acidification augmented antigen/IgE-induced and FcεRI-mediated production of IL-6 and IL-13 in mast cells, and that this was associated with the enhancement of p38 MAPK and Akt activation.

Keywords: Extracellular acidification; IL-13; IL-6; Interleukin; Mast cells; p38 MAPK.

MeSH terms

  • Animals
  • Cell Movement
  • Cells, Cultured
  • Dinitrophenols / pharmacology
  • Hydrogen-Ion Concentration
  • Immunoglobulin E / immunology
  • Immunoglobulin E / metabolism
  • Interleukin-13 / metabolism*
  • Interleukin-6 / metabolism*
  • Mast Cells / chemistry
  • Mast Cells / drug effects
  • Mast Cells / immunology
  • Mast Cells / metabolism*
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, IgE / metabolism*
  • Serum Albumin / pharmacology
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Dinitrophenols
  • GPR4 protein, mouse
  • Interleukin-13
  • Interleukin-6
  • Receptors, G-Protein-Coupled
  • Receptors, IgE
  • Serum Albumin
  • dinitrophenyl-human serum albumin conjugate
  • Immunoglobulin E
  • Proto-Oncogene Proteins c-akt
  • p38 Mitogen-Activated Protein Kinases