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. 2020 Oct 11;24(22):13408–13420. doi: 10.1111/jcmm.15964

FIGURE 3.

FIGURE 3

Depletion of JNK1 reduces ER stress and the production of inflammatory cytokines in HK‐2 cells following hypoxia‐reoxygenation (H/R). HK‐2 cells depleted of JNK1 and vehicle‐infected HK‐2 cells were cultured under normal conditions or subjected to H/R (4 h of hypoxia followed by 12 h reoxygenation). Representative western blots of ER stress markers (A) upstream (GRP78, PERK, ATF6, pIRE1α) and (B) downstream (CHOP) of JNK; β‐actin was used as the loading control. Quantitative analysis of western blots of ER stress markers (C) upstream (GRP78, PERK, ATF6, pIRE1α) and (D) downstream (CHOP) of JNK. E, qRT‐PCR analysis of JNK1, CHOP and ACTB (internal control). F, IL‐6 secretion to the culture supernatant, and qRT‐PCR analysis of IL‐6 and ACTB (internal control). G, MCP‐1 secretion to the culture supernatant, and qRT‐PCR analysis of MCP‐1 and ACTB (internal control). Con: HK‐2 cells without H/R; H/R 12 h: HK‐2 cells with 4 h of hypoxia followed by 12 h of reoxygenation; JNK1 ShRNA: JNK1 shRNA‐infected HK‐2 cells; Vehicle: vehicle‐infected HK‐2 cells.(NS: not significant, **P < .01,***P < .001, ****P < .0001)