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Erlotinib protests against LPS-induced parthanatos through inhibiting macrophage surface TLR4 expression

机译:通过抑制巨噬细胞表面TLR4表达厄洛替尼抗击LPS诱导的副疗法

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摘要

Wild-type C57BL/6 mice were primed with 100 mg kg–1 of erlotinib gavage administration or 3-AB before LPS treatment as described in methods. a After LPS stimulation, survival rate of mice was detected every 6 h for 72 h. LPS + erlotinib group (n = 20) and LPS + 3-AB group (n = 20)’s life span was significantly increased compared to LPS group (n = 20, P < 0.05). b, c After 24 h LPS treatment, peritoneal macrophages were collected and identified with F4/80. Cell death was analyzed by flow cytometry. d, e RAW264.7 cells were treated with LPS for 24 h in the presence or absence of pretreatment of erlotinib or 3-AB for 30 min followed by flow cytometry analysis of cell death. Error bars represent SD (n = 3). *P < 0.05 as compared with Sham; †P < 0.05 as compared with the time-matched LPS group.
机译:如方法中所述,野生型C57BL / 6小鼠用100mg kg-1的欧洛替尼饲养给药或3-ab进行。在LPS刺激后,每6小时检测小鼠的存活率72小时。与LPS组相比,LPS + Erlotinib组(n = 20)和LPS + 3-AB组(n = 20)的寿命显着增加(n = 20,p <0.05)。 B,C 24小时后处理后,收集腹膜巨噬细胞并用F4 / 80鉴定。通过流式细胞术分析细胞死亡。 D,将E Raw264.7细胞用LPS处理24小时,在欧尔替尼或3-AB的预处理中,30分钟后,随后进行细胞死亡的流式细胞术分析。误差栏代表SD(n = 3)。 *与假的P <0.05;与时间匹配的LPS组相比,P <0.05。

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