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. 2013 Dec 2;3:3388. doi: 10.1038/srep03388

Figure 2. PGE2 + IFNγ- or PGE2-induced IL-6 release was enhanced under ER stress.

Figure 2

(A) Glial cells were treated with tunicamycin (Tm: 1 μg/mL) for 1 h and then stimulated with prostaglandin E2 (PGE2: 15 μM) + interferon γ (IFNγ: 20 ng/mL) for 24 h. IL-6 protein levels were detected by ELISA. ER stress increased PGE2 + IFNγ-induced IL-6 release. ***P < 0.001 PGE2 + IFNγv.s. PGE2 + IFNγ + Tm. n = 5. (B) Glial cells were treated with tunicamycin (Tm: 1 μg/mL) for 1 h and then stimulated with PGE2 (15 μM) + IFNγ (20 ng/mL) for 4 h. IL-6 mRNA levels were detected by RT-PCR. Tm increased PGE2 + IFNγ-induced IL-6 expression. ***P < 0.001 PGE2 + IFNγ v.s. PGE2 + IFNγ + Tm. n = 7. The GAPDH was analyzed as loading control. Full-length gels are presented in Supplementary Fig S2. Full-length gels for GAPDH are presented in Supplementary Fig S3. (C) Glial cells were treated with tunicamycin (Tm: 1 μg/mL) for 1 h and then stimulated with PGE2 (15 μM) for 24 h. IL-6 protein levels were detected by ELISA. Tm increased PGE2-induced IL-6 release. **P < 0.01 PGE2v.s. PGE2 + Tm. n = 5. Cropped gels were run under the same experimental conditions.