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Counter‐regulatory paracrine actions of FGF ‐23 and 1,25( OH ) 2 D in macrophages
Author(s) -
Han Xiaobin,
Li Linqiang,
Yang Jiancheng,
King Gwendalyn,
Xiao Zhousheng,
Quarles Leigh Darryl
Publication year - 2016
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1002/1873-3468.12040
Subject(s) - proinflammatory cytokine , arginase , fibroblast growth factor , microbiology and biotechnology , paracrine signalling , macrophage polarization , autocrine signalling , inflammation , immune system , chemistry , macrophage , biology , immunology , biochemistry , arginine , receptor , in vitro , amino acid
Mechanisms underlying the association between fibroblastic growth factor 23 ( FGF ‐23) and inflammation are uncertain. We found that FGF ‐23 was markedly up‐regulated in LPS / INF ‐γ‐induced proinflammatory M1 macrophages and Hyp mouse‐derived peritoneal macrophages, but not in IL ‐4‐induced M2 anti‐inflammatory macrophages. NF ‐КB and JAK / STAT 1 pathways mediated the increased transcription of FGF ‐23 in response to M1 polarization. FGF ‐23 stimulated TNF ‐α, but not IL ‐6, expression in M0 macrophages and suppressed Arginase‐1 expression in M2 macrophages through FGFR ‐mediated mechanisms. 1,25( OH ) 2 D stimulated Arginase‐1 expression and inhibited FGF ‐23 stimulation of TNF ‐α. FGF ‐23 has proinflammatory paracrine functions and counter‐regulatory actions to 1,25( OH ) 2 D on innate immune responses.