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. 2016 Dec 13;14:338. doi: 10.1186/s12967-016-1098-z

Table 2.

The inflammatory signaling pathways and related gene transcripts affected by daily injection of electrolyte solution (Control) compared to Sham

Signaling pathways (p value) Up regulated genes Down regulated genes
Complement (1 × 10 6) C2, C3, C6, C4BPA, CFD, ITGB2, ITGAM, ITGAX C7
B cell development (6 × 10 6) HLA-DRA, HLA-DRB5, HLA-DQB1, IL7, IL7R, PTPRC, SPN
CD28 signaling in Th cells (1 × 10 5) HLA-DRA, HLA-DRB5, HLA-DQB1, CD247, CD3E, CD3G, GRAP2, PAK1, PTPRC, VAV1 Calm1, FOS, PIK3C2G, PIK3R3
ICOs/ICOSL signaling in Th cells (1.3 × 10 5) CD247, CD3E, CD3G, GRAP2, HLA-DQB1, HLA-DRA, HLA-DRB5, PTPRC, VAV1 Calm1, CAMK2D, PIK3C2G, PIK3R3
Nur 77 signaling in T cells (5 × 10 5) CD247, CD3G, HLA-DRA, HLA-DRB5, HLA-DQB1, CD3E Calm1, CASP3
Agranulocyte adhesion and diapedesis (0.0001) ACTC1, AOC3, CCL4, CCL9, EZR, IL18, ITGB2, MYH3 CCL20, CD34, CLDN5, CXCL2, CXCR4, ICAM2, MMP27
Granulocyte adhesion and diapedesis (0.00013) CCL4, CCL9, EZR, IL18, ITGAM, ITGB2 CCL20, CLDN5, CXCL2, CXCR4, ICAM2, IL1R2, MMP27
Cross talk between DCs and NK cells (0.001) ACTG2, HLA-DRA, HLA-DRB5, IL18 IL6, MIBC, FSCN1, CAMK2D, ACTC1, TNFSF10
Antigen presentation pathway (0.001) CIITA, CD74, HLA-DRA, HLA-DRB5
Acute phase response signaling (0.001) AGT, C2, C3, C4BPA, IL18, KLKB1, RBP4, SERPINA3 FOS, IL6, PIK3R3, VWF
Role of hypercytokinemia/hyperchemokinemia in the pathogenesis (0.003162) CCL4, IL18 IL6
TREM1 signaling (0.0631, NS) CIITA, IL18, ITGAX, TLR11 IL6
IL-10 signaling (0.0631, NS) IL18, IL10RA FOS, IL6, IL1R2
Differential regulation of cytokine production in MΦ and Th cell (0.1, NS) CCL4 IL6
IL-6 signaling (0.1259, NS) IL18 IL6, FOS, IL1R2, PIK3C2G, PIK3R3
HMGB1 signaling (0.1259, NS) IL18 IL6, FOS, PIK3C2G, PIK3R3, RHOJ
Inhibition of matrix metalloproteinase (0.2512, NS) THBS2 MMP27
IL-17 signaling in fibroblast (0.2512, NS) IL6, FOS
MIF regulation of innate immunity (0.3162, NS) CD74 FOS
MIF-mediated glucocortical regulation (0.5012, NS) CD74
Toll-like receptor signaling (1.0, NS) IL18 FOS

The affected signaling pathways were ranked from the most (top) to the least significant (bottom) based on the p value

DC dendritic cell, NK natural killer, Th T helper, macrophage, ICOS inducible costimulator, ICOSL inducible costimulatory ligand, TREM1 triggering receptor expressed on myeloid cells 1, MIF macrophage migration inhibitory factor, HMGB1 high mobility group box 1, NS not significant