| Literature DB >> 26196745 |
Yosuke Kamide1, Tamotsu Ishizuka2, Masayuki Tobo3, Hiroaki Tsurumaki4, Haruka Aoki3, Chihiro Mogi3, Takashi Nakakura5, Masakiyo Yatomi6, Akihiro Ono6, Yasuhiko Koga6, Koichi Sato3, Takeshi Hisada6, Kunio Dobashi7, Masanobu Yamada6, Fumikazu Okajima3.
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.Entities:
Keywords: Extracellular acidification; IL-13; IL-6; Interleukin; Mast cells; p38 MAPK
Mesh:
Substances:
Year: 2015 PMID: 26196745 DOI: 10.1016/j.bbrc.2015.07.077
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575