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Sci Rep ; 7(1): 5922, 2017 07 19.
Article in English | MEDLINE | ID: mdl-28725048

ABSTRACT

Eosinophils and their associated cytokines IL-4 and IL-5 are emerging as central orchestrators of the immune-metabolic axis. Herein, we demonstrate that cross-talk between the Ig-superfamily receptor CD300f and IL-5 is a key checkpoint that modifies the ability of eosinophils to regulate metabolic outcomes. Generation of Il5 Tg /Cd300f -/- mice revealed marked and distinct increases in eosinophil levels and their production of IL-4 in the white and brown adipose tissues. Consequently, Il5 Tg /Cd300f -/- mice had increased alternatively activated macrophage accumulation in the adipose tissue. Cd300f -/- mice displayed age-related accumulation of eosinophils and macrophages in the adipose tissue and decreased adipose tissue weight, which was associated with decreased diet-induced weight gain and insulin resistance. Notably, Il5 Tg /CD300f -/- were protected from diet-induced weight gain and glucose intolerance. These findings highlight the cross-talk between IL-5 receptor and CD300f as a novel pathway regulating adipose tissue eosinophils and offer new entry points for therapeutic intervention for obesity and its complications.


Subject(s)
Adipose Tissue/cytology , Eosinophils/metabolism , Interleukin-4/metabolism , Interleukin-5/metabolism , Receptors, Immunologic/metabolism , Animals , Endothelial Cells/metabolism , Extracellular Signal-Regulated MAP Kinases/metabolism , Glucose Intolerance/metabolism , Glucose Intolerance/pathology , Ligands , Macrophages/metabolism , Mice, Inbred C57BL , Mice, Transgenic , Phosphorylation , Proto-Oncogene Proteins c-akt/metabolism , Receptors, Interleukin-5/metabolism , Weight Gain
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