Table 1.
Identifier | Enriched in | FDR | Function in DC | References |
---|---|---|---|---|
mmu-miR-155-5p | LPS-EV | 4.04E−12 | Master regulator in DC maturation | [62] |
mmu-miR-708-3p | VitD3-EV | 2.21E−09 | Downregulated in mature/activated DC | [63] |
mmu-miR-10a-5p | VitD3-EV | 2.31E−07 | Inhibits DC activation and Th1/Th17 cell immune responses | [64] |
mmu-miR-146a-5p | LPS-EV | 4.53E−06 | Down regulates IL-12p70, IL-6, and TNF-α production by DC | [65] |
mmu-miR-9-5p | LPS-EV | 1.86E−05 | Regulatory circuitry controlling monocyte activation by LPS | [66] |
mmu-miR-223-5p | VitD3-EV | 6.82E−05 | Repression of pro-inflammatory cytokine release by DC | [67] |
mmu-miR-378a-3p | VitD3-EV | 8.24E−05 | Upregulated in VitD3-treated DC | [68] |
mmu-miR-203-3p | VitD3-EV | 0.000328 | Upregulated in tolerogenic DC | [69] |
mmu-miR-199a-3p | VitD3-EV | 0.000484 | Upregulated in tolerogenic DC | [69] |
mmu-miR-27b-5p | VitD3-EV | 0.000578 | Suppression of inflammatory cytokine production via NF-κB | [69] |
mmu-miR-7a-5p | LPS-EV | 0.000703 | Upregulated in LPS/IFNg stimulated DC | [69] |
mmu-miR-126a-3p | VitD3-EV | 0.000946 | Reduces the responsiveness of DCs to TLR7/9 ligands | [70] |
mmu-miR-708-5p | VitD3-EV | 0.000946 | Suppresses NF-κB signaling | [71] |
mmu-miR-181b-3p | VitD3-EV | 0.001923 | Inhibition of CD40 and MHCII expression | [72] |
mmu-miR-27a-5p | VitD3-EV | 0.002511 | Suppression of inflammatory cytokine production | [73] |
EV-associated RNA from control, LPS, and VitD3 conditions was isolated and analyzed by RNA sequencing. Read counts for individual RNAs were normalized to the total read counts of each RNA class. LPS- or VitD3-induced fold-changes and corresponding p values were calculated relative to the control condition with edgeR GLM method. We created a top 20 list of miRNAs with the lowest FDR values. Indicated are miRNAs from this top 20 for which DC-related functions have been reported