Shu P, Yuan M, Yang K, He W, Liu L
Graduate School, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Department of Gynecology, First Affiliated Hospital, Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2024 Oct 20;44(10):1874-1880. doi: 10.12122/j.issn.1673-4254.2024.10.05.
To investigate whether quercetin inhibits pyroptosis of mouse fibroblast NIH-3T3 cells by regulating the NLRP3/caspase-1/GSDMD signaling pathway.
NIH-3T3 cells were treated with quercetin or MCC950 (a specific inhibitor of NLRP3) before stimulation with lipopolysaccharide (LPS) and ATP to induce cell pyroptosis. The optimal quercetin concentration and duration were screened using the CCK-8assay after testing various concentrations and times. Morphological changes of the treated cells was observed, and the levels of IL-18 and IL-1β in the cell culture supernatant were detected with ELISA; the protein expressions of NLRP3, cleaved caspase-1, and GSDMD-N and the mRNA levels of NLRP3, caspase-1 and GSDMD were detected using Western blotting and qRT-PCR. The changes in cell pyroptosis were examined with TUNEL staining and LDH release assay.
The CCK-8 assay indicated that 24-hour treatment with 20 μmol/L quercetin yielded the most favorable results. LPS and ATP stimulation of NIH-3T3 cells induced obvious swelling, cell membrane rupture and leakage of cell contents, significantly increased IL-18 and IL-1β levels, and enhanced protein expressions of NLRP3, cleaved caspase-1 and GSDMD-N and mRNA levels of NLRP3, caspase-1 and GSDMD. LPS and ATP stimulation also caused a significant increment of TUNEL-positive cell counts and LDH release in NIH-3T3 cells. Treatment with quercetin or MCC950 significantly reduced cell pyroptosis induced by LPS and ATP, lowered the concentrations of IL-18 and IL-1β, decreased the expression levels of NLRP3, caspase-1/cleaved caspase-1, GSDMD/GSDMD-N, and reduced the number of TUNEL-positive cells and LDH release.
Quercetin suppresses pyroptosis of mouse fibroblasts stimulated with LPS and ATP and reduces secretion of inflammatory cytokines by inhibiting the NLRP3/caspase-1/GSDMD pathway.
探讨槲皮素是否通过调节NLRP3/半胱天冬酶-1/GSDMD信号通路抑制小鼠成纤维细胞NIH-3T3的焦亡。
在用脂多糖(LPS)和ATP刺激诱导细胞焦亡之前,用槲皮素或MCC950(NLRP3的特异性抑制剂)处理NIH-3T3细胞。在测试了不同浓度和时间后,使用CCK-8法筛选槲皮素的最佳浓度和作用时间。观察处理后细胞的形态变化,用ELISA法检测细胞培养上清液中IL-18和IL-1β的水平;用蛋白质免疫印迹法和qRT-PCR检测NLRP3、裂解的半胱天冬酶-1、GSDMD-N的蛋白表达以及NLRP3、半胱天冬酶-1和GSDMD的mRNA水平。用TUNEL染色和LDH释放试验检测细胞焦亡的变化。
CCK-8法表明,用20μmol/L槲皮素处理24小时效果最佳。LPS和ATP刺激NIH-3T3细胞可导致明显肿胀、细胞膜破裂和细胞内容物泄漏,显著增加IL-18和IL-1β水平,并增强NLRP3、裂解的半胱天冬酶-1和GSDMD-N蛋白表达以及NLRP3、半胱天冬酶-1和GSDMD的mRNA水平。LPS和ATP刺激还导致NIH-3T3细胞中TUNEL阳性细胞计数和LDH释放显著增加。用槲皮素或MCC950处理可显著减少LPS和ATP诱导的细胞焦亡,降低IL-18和IL-1β浓度,降低NLRP3、半胱天冬酶-1/裂解的半胱天冬酶-1、GSDMD/GSDMD-N的表达水平,并减少TUNEL阳性细胞数量和LDH释放量。
槲皮素可抑制LPS和ATP刺激的小鼠成纤维细胞焦亡,并通过抑制NLRP3/半胱天冬酶-1/GSDMD途径减少炎性细胞因子的分泌。