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. 2021 Jan 18;11:1740. doi: 10.1038/s41598-021-81039-4

Figure 4.

Figure 4

Transfection of microglia with miR-467f, miR-466q, or exposure to s-EVIFN-γ-MSC, inhibits Map3k8 and Mk2 expression. (a) Scheme of p38 MAPK signaling pathway showing that Map3k8 and Mk2 are specific targets of miR-467f and miR-466q, respectively. (b) Exposure of LPS-activated N9 cells to s-EVIFN-γ-MSC induced a significantly downregulation of Map3k8 and Mk2 mRNA expression. ###P < 0.001, untreated (N9) vs LPS-activated N9 cells (N9 + LPS); **P < 0.01, ***P < 0.001, N9 + LPS vs N9 + LPS exposed to s-EVIFN-γ-MSC (N9 + LPS + s-EVIFN-γ-MSC). (c) Downregulation of Map3k8 and Mk2 mRNA expression in LPS-activated N9 cells transfected with miR-467f and miR-466q confirm that they are target genes for these miRNAs. ###P < 0.001, untreated (N9) vs LPS-activated N9 cells (N9 + LPS); *P < 0.05, **P < 0.01, N9 + LPS vs N9 + LPS transfected with specific miRNA (N9 + LPS + miRNA). (d) Primary microglia obtained from SOD1G93A mice transfected with miR-467f and miR-466q showed a significant downregulation of the expression of genes involved in the p38 MAPK signaling pathway. *P < 0.05, ***P < 0.001, SOD1G93A vs SOD1G93A + miR467f or 466q. Data are presented as mean ± SEM of 3 independent experiments conducted in triplicates.