[HTML][HTML] IL-33 can promote survival, adhesion and cytokine production in human mast cells

M Iikura, H Suto, N Kajiwara, K Oboki, T Ohno… - Laboratory …, 2007 - nature.com
M Iikura, H Suto, N Kajiwara, K Oboki, T Ohno, Y Okayama, H Saito, SJ Galli, S Nakae
Laboratory investigation, 2007nature.com
IL-33 is a recently identified member of the IL-1 family of molecules, which also includes IL-1
and IL-18. IL-33 binds to the receptor, T1/ST2/IL-1R4, and can promote cytokine secretion by
Th2 cells and NF-κB phosphorylation in mouse mast cells. However, the effects of these
molecules, especially IL-33, in human mast cells are poorly understood. Expression of the
receptors for IL-1 family molecules, specifically, IL-1R1, IL-18R and T1/ST2, was detectable
intracellularly in human umbilical cord blood-derived mast cells (HUCBMCs) by flow …
Abstract
IL-33 is a recently identified member of the IL-1 family of molecules, which also includes IL-1 and IL-18. IL-33 binds to the receptor, T1/ST2/IL-1R4, and can promote cytokine secretion by Th2 cells and NF-κB phosphorylation in mouse mast cells. However, the effects of these molecules, especially IL-33, in human mast cells are poorly understood. Expression of the receptors for IL-1 family molecules, specifically, IL-1R1, IL-18R and T1/ST2, was detectable intracellularly in human umbilical cord blood-derived mast cells (HUCBMCs) by flow cytometry, but was scarcely detectable on the cells’ surface. However, IL-1β, IL-18 or IL-33 induced phosphorylation of Erk, p38 and JNK in naïve HUCBMCs, and IL-33 or IL-1β, but not IL-18, enhanced the survival of naive HUCBMCs and promoted their adhesion to fibronectin. IL-33 or IL-1β also induced IL-8 and IL-13 production in naïve HUCBMCs, and enhanced production of these cytokines in IgE/anti-IgE-stimulated HUCBMCs, without enhancing secretion of either PGD 2 or histamine. Moreover, IL-33-mediated IL-8 production by HUCBMCs was markedly reduced by the p38 MAPK inhibitor, SB203580. In contrast to findings with mouse mast cells, IL-18 neither induced nor enhanced secretion of the mediators PGD 2 or histamine by HUCBMCs. Our findings identify previously unknown functions of IL-33 in human mast cells. One of these is that IL-33, like IL-1β, can induce cytokine production in human mast cells even in the absence of stimuli of FcɛRI aggregation. Our findings thus support the hypothesis that IL-33 may enhance mast cell function in allergic disorders and other settings, either in the presence or absence of co-stimulation of mast cells via IgE/antigen–FcɛRI signals.
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