期刊文献+

白藜芦醇对细菌脂多糖耐受的THP-1细胞TNF-α启动子区的影响 被引量:2

Effect of resveratrol on TNF-α promoter region in THP-1 cells tolerant to bacterial lipopolysaccharide
原文传递
导出
摘要 目的:探讨白藜芦醇对细菌脂多糖(LPS)耐受的人原单核细胞THP-1细胞中TNF-α启动子区的影响。方法:首先建立LPS耐受THP-1细胞模型后,然后用LPS分别刺激正常THP-1细胞(对照组)、LPS耐受THP-1细胞(耐受组)、白藜芦醇处理的LPS耐受THP-1细胞(耐受+白藜芦醇组),检测各组细胞TNF-α mRNA的表达及TNF-α启动子区各转录因子的结合情况。结果:LPS刺激后,TNF-α mRNA表达在对照组细胞迅速升高,耐受组缓慢升高,而耐受+白藜芦醇组略微升高,表达量明显低于前两组(均P<0.05)。染色体免疫沉淀(ChIP)分析显示,LPS刺激前,耐受组与耐受+白藜芦醇组p65及乙酰化p65(ace-p65)、Rel B、G9a对TNF-p启动子区的结合量均明显高于对照组(均P<0.05),而p50的结合量各组细胞间无统计学差异(P>0.05);LPS刺激后,p65和ace-p65对TNF-α启动子区的结合量在对照组明显增加,而在耐受+白藜芦醇组明显降低,G9a结合量在对照组量明显降低(均P<0.05),其余转录因子较刺激前无明显改变(均P>0.05)。结论:白藜芦醇可以抑制LPS耐受的THP-1细胞中TNF-α mRNA的表达,可能部分通过抑制p65/ace-p65对TNF-α启动子区的结合。 Objective: To investigate the effect of resveratrol on TNF-α promoter region in human monocyte THP-1 cells tolerated to bacterial lipopolysaccharide(LPS). Methods: The LPS-tolerated THP-1 cells were induced, next the untreated THP-1 cells(control group), LPStolerated THP-1 cells(tolerance group) and resveratrol treated LPS-tolerated THP-1 cells(tolerance plus resveratrol group) were stimulated with LPS respectively, and then, the TNF-α mRNA expression and the bindings of transcription factors to the promoter region of TNF-α were determined.Results: After LPS stimulation, the TNF-α mRNA level was increased rapidly in control group, and increased slowly in tolerance group, but were slightly decreased in tolerance plus resveratrol group, which was significantly lower than that in either former group(both P〈0.05). Results of chromatin immunoprecipitation(Ch IP) showed that before LPS simulation, the levels of p65 along with acetylated p65(ace-p65), Rel B and G9 a binding to the promoter region of TNF-α in both tolerance group and tolerance plus resveratrol group were significantly higher than those in control group(all P〈0.05), while the binding level of p50 had no significant difference among the three groups(P〉0.05); after LPS simulation, the levels of p65 and ace-p65 binding to the promoter region of TNF-α were significantly increased in control group, but significantly decreased in tolerance plus resveratrol group, and level of G9 a binding to the promoter region of TNF-α was decreased in control group(all P〈0.05), and all other factors had no significant change compared with those before LPS stimulation(all P〉0.05). Conclusion: Resveratrol can inhibit TNF-α mRNA expression in LPS-tolered THP-1 cells, which may be partially associated with its inhibiting the bindings of p65/ace-p65 to TNF-α promoter. So, Resveratrol may potentially be used in supplementary treatment of sepsis.
出处 《中国普通外科杂志》 CAS CSCD 北大核心 2016年第5期686-692,共7页 China Journal of General Surgery
基金 国家自然科学基金资助项目(81201250) 国家科技支撑计划资助项目(2012BAI11B05)
关键词 脓毒症 沉默信息调节蛋白质类 白藜芦醇 脂多糖类 Sepsis Silent Information Regulator Proteins Resveratrol Lipopolysaccharides
  • 相关文献

参考文献24

  • 1Suffredini AF, Munford RS. Novel therapies for septic shock over the past 4 decades[J]. JAMA, 2011,306(2):194-199. 被引量:1
  • 2Simon PS, Sharman SK, Lu C, et al. The NF-:B p65 and p50 homodimer cooperate with IRF8 to activate iNOS transcription[J]. BMC Cancer, 2015, 15:770. doi: 10.1186/s12885-015-1808-6. 被引量:1
  • 3Rothgiesser KM, Erener S, Waibel S, et al. SIRT2 regulates NF-:cB dependent gene expression through deacetylation of p65 Lys310[J]. J Cell Sci, 2010, 123(Pt 24):4251-4258. 被引量:1
  • 4Wang W, Bai L, Qiao H, et al. The protective effect of fenofibrate against TNF-ct-induced CD40 expression through SIRT1 mediated deacetylation of NF-:cB in endothelial cells[J]. Inflammation, 2014, 37(1):177-185. 被引量:1
  • 5陈小萍,李明慧,从美丽,康雁君,郭文平,张永振.SIRT1抑制细菌脂多糖耐受THP-1细胞中IL-1βmRNA的转录[J].中华流行病学杂志,2011,32(6):613-616. 被引量:1
  • 6Chen X, El Gazzar M, Yoza BK, et al. The NF-kappaB factor RelB and histone H3 lysine methyltransferase G9a directly interact to generate epigenetic silencing in endotoxin tolerance[J]. J Biol Chem, 2009, 284(41):27857-27865. 被引量:1
  • 7Orecchia A, Scarponi C, Di Felice F, et al. Sirtinol treatment reduces inflammation in human dermal microvascular endothelial cells[J]. PLoS One, 2011, 6(9):e24307. doi: 10.1371/journal.pone.0024307. E1. 被引量:1
  • 8Gazzar M, Yoza BK, Chen X, et al. G9a and HP1 couple histone and DNA methylation to TNFalpha transcription silencing during endotoxin tolerance[J]. J Biol Chem, 2008, 283(47):32198-32208. 被引量:1
  • 9Fei Y, Wang W, Kwiecinski J, et al. The combination of a tumor necrosis factor inhibitor and antibiotic alleviates staphylococcal arthritis and sepsis in mice[J]. J Infect Dis, 2011,204(3):348-357. 被引量:1
  • 10Sprung CL, Annane D, Keh D, et al. Hydrocortisone therapy for patients with septic shock[J]. N Engl J Med, 2008, 358(2): 111-124. 被引量:1

二级参考文献17

  • 1Yoza BK, McCall CE. Facultative heterochromatin formation at the IL-1 beta promoter in LPS tolerance and sepsis. Cytokine, 2011,53(2) : 145-152. 被引量:1
  • 2Choi KC, Jung MG, Lee YH, et al. Epigallocatechin-3-gallate, a histone acetyltransferase inhibitor, inhibits EBV-induced B lymphocyte transformation via suppression of RelA acetylation. Cancer Res, 2009,69 (2) : 583 -592. 被引量:1
  • 3Salminen A, Kauppinen A, Suuronen T, et al. SIRTI longevity factor suppresses NF-kappaB-driven immune responses: regulation of aging via NF-kappaB acetylation? Bioessays, 2008.30(10) : 939-942. 被引量:1
  • 4LaRue KE, McCall CE. A labile transcriptional repressor modulates endotoxin tolerance. J Exp Med, 1994, 180(6) :2269-2275. 被引量:1
  • 5Dittenhafer-Reed KE, Feldman JL, Denu JM. Catalysis and mechanistic insights into sirtuin activation. Chembiochem, 2011, 12(2) :281-289. 被引量:1
  • 6Saunders LR, Verdin E. Sirtuins: critical regulators at lhe crossroads between cancer and aging. Oncogene, 2007,26(37) : 5489-5504. 被引量:1
  • 7Lavu S, Boss O, Elliott P J, et al. Sirtuins-novel therapeutic targets to treat age-associated diseases. Nat Rev Drug Discov, 2008, 7 (10) :841-853. 被引量:1
  • 8Haigis MC, Guarente LP. Mammalian sirtuins--emerging roles in physiology, aging, and calorie restriction. Genes Dev, 2006, 20 (21) :2913-2921. 被引量:1
  • 9Rajendrasozhan S, Yang SR, Kinnula VL, et al. SIRT1, an antiinflammatory and antiaging protein, is decreased in lungs of patients with chronic obstructive pulmonary disease. Am J Respir Crit Care Med, 2008,177 ( 8 ) : 861-870. 被引量:1
  • 10Shen Z,Ajmo JM,Rogers CQ,et al. Role of SIRT1 in regulation of LPS- or two ethanol metabolites-induced TNF-alpha production in cultured macrophage cell lines. Am J Physiol Gastrointest Liver Physiol, 2009,296 ( 5 ) : 1047-1053. 被引量:1

同被引文献13

引证文献2

二级引证文献14

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