Orai and TRPC channel characterization in Fc<i>ε</i>RI‐mediated calcium signaling and mediator secretion in human mast cells

Abstract

Abstract Inappropriate activation of mast cells via the Fc ε RI receptor leads to the release of inflammatory mediators and symptoms of allergic disease. Calcium influx is a critical regulator of mast cell signaling and is required for exocytosis of preformed mediators and for synthesis of eicosanoids, cytokines and chemokines. Studies in rodent and human mast cells have identified Orai calcium channels as key contributors to Fc ε RI ‐initiated mediator release. However, until now the role of TRPC calcium channels in Fc ε RI ‐mediated human mast cell signaling has not been published. Here, we show evidence for the expression of Orai 1,2, and 3 and TRPC 1 and 6 in primary human lung mast cells and the LAD 2 human mast cell line but, we only find evidence of functional contribution of Orai and not TRPC channels to Fc ε RI ‐mediated calcium entry. Calcium imaging experiments, utilizing an Orai selective antagonist (Synta66) showed the contribution of Orai to Fc ε RI ‐mediated signaling in human mast cells. Although, the use of a TRPC 3/6 selective antagonist and agonist ( GSK ‐3503A and GSK ‐2934A, respectively) did not reveal evidence for TRPC 6 contribution to Fc ε RI ‐mediated calcium signaling in human mast cells. Similarly, inactivation of STIM 1‐regulated TRPC 1 in human mast cells (as tested by transfecting cells with STIM 1‐ KK 684‐685 EE ‐ TRPC 1 gating mutant) failed to alter Fc ε RI ‐mediated calcium signaling in LAD 2 human mast cells. Mediator release assays confirm that Fc ε RI ‐mediated calcium influx through Orai is necessary for histamine and TNF α release but is differentially involved in the generation of cytokines and eicosanoids.