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- W2938651496 endingPage "341" @default.
- W2938651496 startingPage "341" @default.
- W2938651496 abstract "Clinically relevant exocytosis of mast cell (MC) mediators can be triggered by high-affinity IgE receptor (FcεRI)-aggregation (allergic route) or by the so-called pseudo-allergic pathway elicited via MAS-related G protein-coupled receptor-X2 (MRGPRX2). The latter is activated by drugs and endogenous neuropeptides. We recently reported that FcεRI-triggered degranulation is attenuated when human skin mast cells are chronically exposed to IL-33. Here, we were interested in the regulation of the MRGPRX2-route. Chronic exposure of skin MCs to IL-33 basically eliminated the pseudo-allergic/neurogenic route as a result of massive MRGPRX2 reduction. This downregulation seemed to partially require c-Jun N-terminal Kinase (JNK), but not p38, the two kinases activated by IL-33 in skin MCs. Surprisingly, however, JNK had a positive effect on MRGPRX2 expression in the absence of IL-33. This was evidenced by Accell®-mediated JNK knockdown and JNK inhibition. In stark contrast to the dampening effect upon prolonged exposure, IL-33 was able to prime for increased degranulation by MRGPRX2 ligands when administered directly before stimulation. This supportive effect depended on p38, but not on JNK activity. Our data reinforce the concept that exposure length dictates whether IL-33 will enhance or attenuate secretion. IL-33 is, thus, the first factor to acutely enhance MRGPRX2-triggered degranulation. Finally, we reveal that p38, rarely associated with MC degranulation, can positively affect exocytosis in a context-dependent manner." @default.
- W2938651496 created "2019-04-25" @default.
- W2938651496 creator A5004739251 @default.
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- W2938651496 creator A5015855045 @default.
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- W2938651496 date "2019-04-11" @default.
- W2938651496 modified "2023-10-03" @default.
- W2938651496 title "IL-33 and MRGPRX2-Triggered Activation of Human Skin Mast Cells—Elimination of Receptor Expression on Chronic Exposure, but Reinforced Degranulation on Acute Priming" @default.
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- W2938651496 doi "https://doi.org/10.3390/cells8040341" @default.
- W2938651496 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6523246" @default.
- W2938651496 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30979016" @default.
- W2938651496 hasPublicationYear "2019" @default.
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