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Article Abstract

ST2 memory-type Th2 cells are identified as a pathogenic subpopulation in eosinophilic airway inflammation. These ST2 pathogenic Th2 cells produce large amount of IL-5 upon T cell receptor stimulation, but not in response to IL-33 treatment. By contrast, IL-33 alone induces cytokine production in ST2 group 2 innate lymphoid cells (ILC2). Here we show that a MAPK phosphatase Dusp10 is a key negative regulator of IL-33-induced cytokine production in Th2 cells. In this regard, Dusp10 is expressed by ST2 pathogenic Th2 cells but not by ILC2, and Dusp10 expression inhibits IL-33-induced cytokine production. Mechanistically, this inhibition is mediated by DUSP10-mediated dephosphorylation and inactivation of p38 MAPK, resulting in reduced GATA3 activity. The deletion of Dusp10 renders ST2 Th2 cells capable of producing IL-5 by IL-33 stimulation. Our data thus suggest that DUSP10 restricts IL-33-induced cytokine production in ST2 pathogenic Th2 cells by controlling p38-GATA3 activity.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185962PMC
http://dx.doi.org/10.1038/s41467-018-06468-8DOI Listing

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