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阿法替尼调控Egr-1/TLR4/mTOR信号通路抑制肝癌细胞Hep3B增殖迁移侵袭及促进细胞凋亡的机制 被引量:3
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作者 李晶 赵静 孟德峰 《中西医结合肝病杂志》 CAS 2021年第10期917-921,共5页
目的:探讨阿法替尼是否通过早期生长反应因子1(Egr1)/Toll样受体4(TLR4)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路,抑制肝癌细胞Hep3B增殖迁移侵袭并促进其细胞凋亡。方法:采用不同浓度的阿法替尼处理Hep3B细胞,用免疫印迹试验(Western Bl... 目的:探讨阿法替尼是否通过早期生长反应因子1(Egr1)/Toll样受体4(TLR4)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路,抑制肝癌细胞Hep3B增殖迁移侵袭并促进其细胞凋亡。方法:采用不同浓度的阿法替尼处理Hep3B细胞,用免疫印迹试验(Western Blot)检测细胞周期蛋白D1(CyclinD1)、活化的(Cleaved)-天冬氨酸特异性半胱氨酸蛋白酶-3(caspase-3)、基质金属蛋白酶(MMP)-2、MMP9、Egr-1、TLR4、mTOR蛋白的表达,用噻唑蓝(MTT)法检测细胞增殖,流式细胞仪分析细胞凋亡,Transwell测定细胞迁移侵袭。在Hep3B细胞中转染pcDNA-Egr-1,并使用2.0μmol/L阿法替尼处理,采用上述方法检测细胞的增殖、迁移侵袭和凋亡。结果:阿法替尼显著降低Hep3B细胞的CyclinD1、MMP2、MMP9、Egr-1、TLR4、mTOR蛋白含量、增殖活性、细胞迁移及侵袭数量,显著提高Cleaved-caspase-3蛋白含量和凋亡率(P<0.05)。pcDNA-Egr-1可以逆转阿法替尼对Hep3B细胞增殖、迁移侵袭、凋亡和Egr-1/TLR4/mTOR信号通路的影响。结论:阿法替尼可以抑制肝癌细胞Hep3B的增殖,迁移侵袭,并诱导其凋亡,其机制与下调Egr-1/TLR4/mTOR信号通路有关。 展开更多
关键词 阿法替尼 egr-1/tlr4/mtor信号通路 肝癌细胞 增殖 迁移侵袭 凋亡
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Effects of Liancao-Xieli capsule on intestinal mucosal inflammatory factors and TLR4/PI3K/Akt/mTOR signaling pathway in mice with ulcerative colitis
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作者 Jing-Yu Zhan Xing-Xing Yuan +2 位作者 Bing-Yu Wang Chang-Fa Liu Ya-Li Zhang 《Journal of Hainan Medical University》 2021年第24期27-31,共5页
Objective:To observe the effect of Liancao-Xieli capsule on intestinal mucosal inflammatory factors and TLR4/PI3K/Akt/mTOR signaling pathway in mice with ulcerative colitis(UC);Methods:40 male C57BL/6 mice were random... Objective:To observe the effect of Liancao-Xieli capsule on intestinal mucosal inflammatory factors and TLR4/PI3K/Akt/mTOR signaling pathway in mice with ulcerative colitis(UC);Methods:40 male C57BL/6 mice were randomly divided into the control group,model group,Liancao-Xieli group and mesalazine group,with 10 mice in each group.In addition to the control group,the remaining three groups of mice were induced by 3%dextran sulfate sodium(DSS)to induce acute UC model.During the modeling period,mice in each group were given corresponding drugs and normal saline by gavage.At the end of the experiment,HE staining was used to observe the pathological changes of colonic tissue in each group,and ELISA was used to detect the inflammatory factors(TNF-α,IL-6,IL-1β,IL-8,IL-17,and INF-γ)in serum and colonic tissue.The expression levels of TLR4/PI3K/Akt/mTOR signaling pathway related proteins were also detected by Western blot;Results:Compared with the model group,Liancao-Xieli capsule could significantly increase the colon length and decrease the score of colon histopathology in UC mice(P<0.01).In addition,the levels of TNF-α,IL-6,IL1β,IL-8,IL-17,and INF-γwere significantly reduced in serum and colon tissue,and the expressions of TLR4,PI3K,p-Akt and p-mTOR were significantly down-regulated in LiancaoXieyi group when compared with the model group(P<0.01).While the expressions of Akt and mTOR were not significantly affected in Liancao-Xieyi group(P>0.05);Conclusion:LiancaoXieli capsule can reduce the secretion of inflammatory factors,improve the intestinal mucosal damage and inflammatory response in UC by inhibiting the activation of TLR4/PI3K/Akt/mTOR signaling pathway。 展开更多
关键词 Liancao-Xieli capsule Ulcerative colitis Inflammatory factors tlr4/PI3K/Akt/mtor signaling pathway
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Ramulus Cinnamomi extract attenuates neuroinflammatory responses via downregulating TLR4/MyD88 signaling pathway in BV2 cells 被引量:5
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作者 Huan Yang Xiao Cheng +2 位作者 Ying-lin Yang Yue-hua Wang Guan-hua Du 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第11期1860-1864,共5页
Ramulus Cinnamomi (RC), a traditional Chinese herb, has been used to attenuate inflammatory responses. The purpose of this study was to investigate the effect of RC extract on lipopolysaccharide (LPS)-induced neur... Ramulus Cinnamomi (RC), a traditional Chinese herb, has been used to attenuate inflammatory responses. The purpose of this study was to investigate the effect of RC extract on lipopolysaccharide (LPS)-induced neuroinflammation in BV2 microglial cells and the underlying mechanisms involved. BV2 cells were incubated with normal medium (control group), LPS, LPS plus 30 pg/mL RC extract, or LPS plus 100 pg/mL RC extract. The BV2 cell morphology was observed under an optical microscope and cell viability was detected by MTT assay. Nitric oxide level in BV2 cells was detected using Griess regents, and the levels of interleukin-6, interleukin-1 β, and tumor necrosis factor u in BV2 cells were determined by ELISA. The expression levels of cyclooxygenase-2, Toll-like receptor 4 and myeloid differentiation factor 88 proteins were detected by western blot assay. Compared with the LPS group, both 30 and 100 μg/mL RC extract had no significant effect on the viability of BV2 cells. The levels of nitric oxide, interleukin-6, interleukin-1β and tumor necrosis factor ct in BV2 cells were all significantly increased after LPS induction, and the levels were significantly reversed after treatment with 30 and 100 μg/mL RC extract. Furthermore, RC extract significantly inhibited the protein expression levels of cyclooxygenase-2, Toll-like receptor 4 and myeloid differentiation factor 88 in LPS-induced BV2 cells. Our findings suggest that RC extract alleviates neuroinflammation by downregulating the TLR4/MyD88 signaling pathway. 展开更多
关键词 nerve regeneration Ramulus Cinnamomi BV2 cells LIPOPOLYSACCHARIDE NEUROINFLAMMATION pro-inflammatory factors tlr4/ MyD88 signaling pathway nitric oxide INTERLEUKIN-6 INTERLEUKIN-1Β tumor necrosis factor a neuronal regeneration
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