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. 2021 May 4;27(7):842–856. doi: 10.1111/cns.13645

FIGURE 7.

FIGURE 7

Galectin‐1 attenuated the transcriptional activity and translocation of c‐Jun and translocation (n = 3 in each group). Representative immunoblot images of c‐Jun and p65 expression in cytoplasm of BV2 cells (A). The quantitative analysis of c‐Jun (B) and p65 (C) in cytoplasm of BV2 cells. Representative immunoblot images of c‐Jun and p65 expression in nucleus of BV2 cells (D). The quantitative analysis of c‐Jun (E) and p65 (F) in nucleus of BV2 cells. BV2 cells were co‐transfected with Renilla luciferase plasmid (pRL‐SV40‐C) and AP‐1 luciferase reporter plasmid or NF‐κB luciferase reporter plasmid for 48 h, and NF‐κB (G) and c‐Jun (H) reporter activities were analyzed following LPS stimulation. Data are presented as the mean ±SD. *p < 0.05 versus the control and galectin‐1 groups, # p < 0.05 versus the LPS group