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. 2022 Jan 21;177:106092. doi: 10.1016/j.phrs.2022.106092

Fig. 6.

Fig. 6

KD inhibited DC cross-priming of HSC responses via reduction of IL-12 release from DCs. (A) Transcript levels of α-SMA, TGF-β1, and TIMP-1 in JS-1, as assessed by qPCR. (B) Extracellular secretion level of Col-I, TGF-β1, and TIMP-1 in JS-1 tested by ELISA. (C-D) Protein levels of α-SMA in JS-1, as detected by WB and immunofluorescence. JS-1, with or without IL-12, was co-cultured with DCs isolated from normal or LF mice pre-treated with KD, si-IL-12, or KD+si-IL-12. Data expressed as mean ± SD (n = 6). **P < 0.01 relative to normal DCs group; ##P < 0.01 relative to LF DCs group. n.s., not significant.