期刊文献+

人肠道来源艰难梭菌感染Caco-2细胞对NF-κB信号通路相关蛋白表达的影响

The Effect of Human Intestinal Tract-derived Clostridioides difficile Mediated-infection on the Expression Levels of NF-κB Signaling Pathway-related Proteins in Caco-2 Cells
下载PDF
导出
摘要 目的:研究人肠道来源艰难梭感染Caco-2细胞对NF-κB信号通路相关蛋白表达的影响。方法:用艰难梭菌毒素A和毒素B感染Caco-2细胞24 h,以未感染艰难梭菌毒素A和毒素B的Caco-2细胞为对照组,蛋白质免疫印迹法检测真核细胞核因子(NF-κB)通路蛋白P-p65和p65的表达;Caco-2细胞用6孔板制作爬片,待细胞长满6孔板后,以感染复数(MOI)=100加入艰难梭菌,与Caco-2细胞共培养3、6、9、12及24 h,革兰染色后油镜观察,记录黏附细菌数与细胞数,计算共培养时间与细菌黏附数量之间的关系;艰难梭菌感染Caco-2细胞12 h,以Caco-2为对照组,蛋白质免疫印迹法检测NF-κB通路蛋白P-p65、p65、IKKα及IκBα的表达。结果:艰难梭菌与Caco-2细胞共培养12 h时黏附数最多,P-p65和IKKα蛋白表达增加(P<0.05),p65和IκBα蛋白表达降低,差异有统计学意义(P<0.05)。结论:人源艰难梭菌感染Caco-2细胞可激活NF-κB信号通路。 Objective:To study the effect of human intestinal tract-derived Clostridioides difficile mediated-infection on expression of NF-κB signaling pathway-related proteins in Caco-2 cells.Methods:Caco-2 cells were infected with C.difficile toxin A and toxin B for 24 h.Uninfected Caco-2 cells were used as a control group.Western blot was used to detect NF-κB pathway-related proteins such as p65,p65.In addition,Caco-2 cells grown full on 6-well plate were co-cultured with C.difficile with MOI 100 for 3,6,9,12 and 24 h,stained with Gram staining kit and observed under oil microscope.The number of adhered bacteria and the number of cells were recorded.The relationship between co-cultivation time and the number of adhered bacteria was analyzed.At 12 h post-infection with C.difficile,the expression levels of phospho-p65,p65,IKKαand IκBαwere measured by Western blot.Results:The adherence of C.difficile on Caco-2 cells reached the maximum at 12 h after-infection.The expression levels of phospho-p65 and IKKαproteins were significantly increased(P<0.05),while the expression of p65 and IκBαproteins were significantly decreased(P<0.05).Conclusion:C.difficile infection activates NF-κB signaling pathway in Caco-2 cells.
作者 洪伟 饶凤琴 吴昌学 赵行行 程玉梅 张婷 齐晓岚 禹文峰 官志忠 HONG Wei;RAO Fengqin;WU Changxue;ZHAO Xingxing;CHEN Yumei;ZHANG Ting;QI Xiaolan;YU Wenfeng;GUAN Zhizhong(Key Laboratory of Endemic and Ethnic Diseases,Ministry of Education,and Key Laboratory of Medical Molecular Biology,Guizhou Province,Guizhou Medical University,Guiyang 550004,China;Department of Critical Care Medicine,the Affiliate Hospital of Guizhou Medical University,Guiyang,550004,China)
出处 《贵州医科大学学报》 CAS 2019年第12期1365-1369,共5页 Journal of Guizhou Medical University
基金 国家自然科学基金(31560318,31601012,31760318) 贵州省自然科学基金资助项目[黔科合基础(2019)1441,(2018)1132,(2018)5779-17]
关键词 人源艰难梭菌 肠上皮细胞 炎症 凋亡 NF-ΚB信号通路 C.difficile intestinal epithelial cells inflammation apoptosis NF-κB signaling pathway
  • 相关文献

参考文献10

二级参考文献273

  • 1杨志峰,蔡在龙,毛积芳.NF-κB的结构功能及其与疾病的关系[J].生命的化学,2004,24(4):347-349. 被引量:16
  • 2Jia-DingMao,PeiWu,Xiang-HouXia,Ji-QunHu,Wen-BinHuang,Guo-QiangXu.Correlation between expression of gastrin, somatostatin and cell apoptosis regulation gene bcl-2/bax in large intestine carcinoma[J].World Journal of Gastroenterology,2005,11(5):721-725. 被引量:27
  • 3史艳晖,卢圣栋.转录因子NF-κB的研究现状及其应用前景[J].中国生物工程杂志,2007,27(4):110-114. 被引量:42
  • 4苏剑东,吴灵飞.NF-kB与细胞凋亡[J].世界华人消化杂志,2007,15(12):1411-1416. 被引量:51
  • 5De Smaele E, Zazzeroni F, Papa S, et al. Induction of gadd45β by NF-κB downregulates pro-apoptotic JNK signaling. Nature, 2001,414:308-313.
  • 6Duckett C S, Thompson C B. CD30-dependent degradation of TRAF2: implications of negtive regulation of TRAF signaling and the control of cell survival. Genes Dev, 1997, 11:2810-2821.
  • 7Leo E, Deveraux Q L, Buchholtz C, et al. TRAFI is a substrate of caspases activated during TNF-obinduced apoptosis. J Biol Chem,2001, 276:8087-8093.
  • 8Tang G, Yang J, Minemoto Y, et al. Blocking caspase-3-mediated proteolysis of IKK- suppresses TNFα-induced apoptosis. Mol Cell, 2001, 8:1005-1016.
  • 9Reuther J Y, Baldwin A S. Apoptosis promotes a caspase-induced amino-terminal truncation of It.Bet that functions as a stable inhibitor of NF-κB. J Biol Chem, 1999, 274:20664-20670.
  • 10Barkett M, Xue D, Horvitz H R, et al. Phosphorylation of IκBα inhibits its cleavage by caspase CPP32 in vitro. J Biol Chem, 1997,272:29419-29422.

共引文献296

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部