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Foxo4‐ and Stat3‐dependent IL‐10 production by progranulin in regulatory T cells restrains inflammatory arthritis
Author(s) -
Fu Wenyu,
Hu Wenhuo,
Shi Lei,
Mundra Jyoti Joshi,
Xiao GuoZhi,
Dustin Michael L.,
Liu Chuanju
Publication year - 2017
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.201601134r
Subject(s) - stat3 , inflammation , arthritis , immunology , cytokine , biology , stat protein , mediator , inflammatory arthritis , interleukin 17 , cancer research , signal transduction , microbiology and biotechnology
Progranulin (PGRN) restrains inflammation and is therapeutic against inflammatory arthritis; however, the underlying immunological mechanism remains unknown. In this study, we demonstrated that anti‐inflammatory cytokine IL‐10 was a critical mediator for PGRN‐mediated anti‐inflammation in collagen‐induced arthritis by using PGRN and IL‐10 genetically modified mouse models. IL‐10 green fluorescent protein reporter mice revealed that regulatory T (T reg ) cells were the predominant source of IL‐10 in response to PGRN. In addition, PGRN‐mediated expansion and activation of T reg cells, as well as IL‐10 production, depends on JNK signaling, but not on known PGRN‐activated ERK and PI3K pathways. Furthermore, microarray and chromatin immunoprecipitation sequencing screens led to the discovery of forkhead box protein O4 and signal transducer and activator of transcription 3 as the transcription factors required for PGRN induction of IL‐10 in T reg cells. These findings define a previously unrecognized signaling pathway that underlies IL‐10 production by PGRN in T reg cells and present new insights into the mechanisms by which PGRN resolves inflammation in inflammatory conditions and autoimmune diseases, particularly inflammatory arthritis. —Fu, W., Hu, W., Shi, L., Mundra, J. J. Xiao, G., Dustin, M. L., Liu, C. Foxo4‐ and Stat3‐dependent IL‐10 production by progranulin in regulatory T cells restrains inflammatory arthritis. FASEB J . 31, 1354–1367 (2017) www.fasebj.org