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

Table 6.

The inflammatory signaling pathways and related gene transcripts affected by daily injection of PYS compared to Control

Signaling pathways (p value) Up regulated genes Down regulated genes
Granulocyte adhesion and diapedesis (1.32 × 10 6) SELL, VCAM1, CXCL13, CXCR2, CXCL14, CCL21, CXCL3, TNF, MMP9, CCL19, TNFRSF11B MMP27, THY1
Agranulocyte adhesion and diapedesis (7.4 × 10 5) SELL, VCAM1, CXCL13, CXCR2, CXCL14, CCL21, CXCL3, TNF, MMP9, CCL19 MMP27
Role of hypercytokinemia/hyperchemokinemia in the pathogenesis (0.4539, NS) TNF
Acute phase response signaling (7.8 × 10 7) SOCS3, HP, C3, ORM1, Saa3, CFB, TNF, A2M, RBP1, FGG, TNFRSF11B NFKBIA, CRABP1
Complement (0.0933, NS) C3, CFB
IL-10 signaling (0.0692, NS) SOCS3, TNF NFKBIA
Differential regulation of cytokine production in MΦ and Th cell (0.2239, NS) TNF
B cell development (0.0851, NS) SPN, HLA-DRA
Inhibition of matrix metalloproteinase (0.0002) TIMP1, A2M, MMP9 MMP27, ADAM12,
Cross talk between DCs and NK cells (0.0083) TNF HLA-DRA, CD226, HLA-E, IL4
TREM1 signaling (0.2818, NS) TNF Tlr11
ICOs/ICOSL signaling in Th cells (0.0912, NS) CAMK4, PIK3C2G NFKBIA, HLA-DRA
Antigen presentation pathway (0.0933, NS) HLA-DRA, HLA-E
IL-6 signaling (0.0021) SOCS3, CSNK2A1, PIK3C2G, A2M, TNF, TNFRSF11B NFKBIA
CD28 signaling in Th cells (0.1117, NS) CAMK4, PIK3C2G NFKBIA, HLA-DRA
Toll-like receptor signaling (0.2767, NS) TNF NFKBIA
IL-17 signaling in fibroblast (0.0126) LCN2, CEBPD NFKBIA
MIF-mediated glucocortical regulation (0.0776, NS) PLA2G2A NFKBIA
MIF regulation of innate immunity (0.0195) NOS2, PLA2G2A NFKBIA
HMGB1 signaling (0.0389) VCAM1, PIK3C2G, TNF, TNFRSF11B IL4
Nur 77 signaling in T cells (0.1995, NS) CAMK4 HLA-DRA

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