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Carnosol inhibits inflammasome activation by directly targeting HSP90 to treat inflammasome-mediated diseases

机译:鼠尾草酚通过直接靶向HSP90来治疗炎症小体介导的疾病从而抑制了炎症小体的活化

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摘要

Western blot analysis of caspase-1 (p20) and IL-1β in culture supernatants (Sup.) and pro- IL-1β, caspase-1 (p45), NLRP3 and ASC in cell lysates (Lys.) of LPS-primed BMDMs treated with various doses of carnosol and then stimulated with nigericin. – Activity of caspase-1 ( ), ELISA of IL-1β ( ), release of LDH ( ) and ELISA of TNF-α ( ) in Sup. from samples described in . Western blot analysis of caspase-1 (p20) and IL-1β in Sup. and pro- IL-1β, caspase-1 (p45), NLRP3 and ASC in cell Lys. of PMA-primed THP1 treated with various doses of carnosol and then stimulated with nigericin. – Activity of caspase-1 ( ), ELISA of IL-1β ( ) and TNF-α ( ) in Sup. from samples described in . , Activity of caspase-1 ( ) and ELISA of IL-1β ( in Sup. from LPS-primed hPBMCs treated with various doses of carnosol and then stimulated with nigericin. Coomassie blue staining was used as the loading control in Sup. GAPDH served as a loading control in the Lys. Data are represented as the mean ± SD from at least four biological samples. The significance of the differences was analyzed using Mann–Whitney test: *  P P
机译:对培养上清液中的caspase-1(p20)和IL-1β(补充)和LPS引发的BMDMs的细胞裂解液(Lys。)中的pro-IL-1β,caspase-1(p45),NLRP3和ASC进行蛋白质印迹分析用各种剂量的鼠尾草酚处理,然后用尼日菌素刺激。 – Sup中的caspase-1()活性,IL-1β()ELISA,LDH()释放和TNF-α()ELISA。从样品中描述。 Sup中caspase-1(p20)和IL-1β的蛋白质印迹分析。细胞Lys中的前IL-1β,caspase-1(p45),NLRP3和ASC。 PMA引发的THP1进行了不同剂量的鼠尾草酚处理,然后用黑霉素进行了刺激。 – Sup中的caspase-1()活性,IL-1β()和TNF-α()的ELISA。从样品中描述。 ,Caspase-1()活性和IL-1β(ELISA)分别来自用不同剂量的鼠尾草酚处理后再用尼日利亚霉素刺激的LPS引发的hPBMC,考马斯亮蓝染色作为Sup的上样对照,GAPDH作为Lys中的上样对照,数据表示为至少四个生物学样品的平均值±SD,使用Mann–Whitney检验分析差异的显着性:

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