| Literature DB >> 31030957 |
Daniel Abebayehu1, Andrew J Spence1, Heather Caslin1, Marcela Taruselli1, Tamara T Haque1, Kasalina N Kiwanuka1, Elizabeth Motunrayo Kolawole1, Alena P Chumanevich2, Scott A Sell3, Carole A Oskeritzian2, John Ryan4, Sydney Ann Kee1.
Abstract
Mast cells have functional plasticity affected by their tissue microenvironment, which greatly impacts their inflammatory responses. Because lactic acid (LA) is abundant in inflamed tissues and tumors, we investigated how it affects mast cell function. Using IgE-mediated activation as a model system, we found that LA suppressed inflammatory cytokine production and degranulation in mouse peritoneal mast cells, data that were confirmed with human skin mast cells. In mouse peritoneal mast cells, LA-mediated cytokine suppression was dependent on pH- and monocarboxylic transporter-1 expression. Additionally, LA reduced IgE-induced Syk, Btk, and ERK phosphorylation, key signals eliciting inflammation. In vivo, LA injection reduced IgE-mediated hypothermia in mice undergoing passive systemic anaphylaxis. Our data suggest that LA may serve as a feedback inhibitor that limits mast cell-mediated inflammation.Entities:
Keywords: Allergy; Anaphylaxis; Asthma; Inflammation; Lactate
Mesh:
Substances:
Year: 2019 PMID: 31030957 PMCID: PMC6579658 DOI: 10.1016/j.cellimm.2019.04.006
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868