Quantitative proteomics and phosphoproteomics reveal glucocorticoid stimulation of TLR and Rho GTPase signaling in neutrophil-like cells

BackgroundGlucocorticoids (GCs) are corticosteroid hormones that are commonly used for treating systemic inflammatory diseases and acute infections. Immunosuppressive effects of GCs have been studied in many cell types, particularly macrophages and T cells. Despite the importance and abundance of neutrophils in the human immune system, GC responses remain understudied in neutrophils. ResultsHere, we performed quantitative mass-spectrometry (MS)-based proteomics of neutrophil-like cells (NLCs) differentiated from human HL-60 promyelocyte cells. Proteome and flow cytometry analysis showed that NLCs share features of neutrophils. Quantitative proteomics and phosphoproteomics of NLCs treated with two synthetic GC compounds, the clinical drugs dexamethasone (DEX) and prednisolone (PRED), identified higher numbers of significantly regulated proteins and phosphosites compared to parental HL-60 cells. GC treatments triggered abnormal neutrophil activation and aging by promoting toll-like receptor (TLR) signaling and CXCR4 serine phosphorylation. We also identified RIPOR2 as a novel target protein of GC which stimulates Rho GTPase signaling networks and upregulates actin cytoskeletal proteins. ConclusionsOur results not only reveal unconventional regulatory mechanism of GCs in the human immune system but also provide valuable resources for discovering novel GC-responsive protein targets.