期刊文献+

LPS耐受巨噬细胞致炎和抗炎细胞因子表达和分泌的特点 被引量:3

Expression and secretion pattern of proinflammatory and anti-inflammatory cytokines in lipopolysaccharidetolerized macrophages
下载PDF
导出
摘要 目的:分析巨噬细胞LPS耐受形成过程中致炎和抗炎细胞因子(TNF-α、IL-6和IL-10)释放的特点和规律,探讨其在巨噬细胞建立LPS耐受机制中的作用。方法:培养小鼠腹腔巨噬细胞系RAW264.7细胞。实验分为两部分:①LPS刺激细胞不同时间(4 h,8 h,20 h)或用PBS培养细胞4 h;②IPS耐受实验(LPS预刺激巨噬细胞20 h后,换液并洗去LPS,再次加入LPS刺激4 h)。ELISA法检测细胞培养上清中TNF-α、IL-6和IL-10的浓度,RT-PCR法相对定量分析巨噬细胞TNF-α和IL-10 mRNA表达水平。结果:细胞培养上清中TNF-α、IL 6和IL-10的浓度随着IPS刺激时间的延长而增加;LPS刺激20 h后建立耐受的巨噬细胞再次受到LPS打击时,其TNF-α释放量低于非耐受细胞,而IL-6和IL-10释放量则大幅增加,与TNF-α释放减少截然相反。TNF-α和IL-10 mRNA表达水平与其蛋白分泌量呈现相似的变化规律。结论:巨噬细胞对LPS的耐受建立在致炎因子和抗炎因子共同作用的基础上;LPS预刺激细胞再次受到LPS打击时,抑炎因子表达和分泌大幅增加是介导巨噬细胞对LPS耐受的重要机制。 Objective: To analyze the patterns of TNF, IL-6 and IL-10 secretion and their mRNA expression in endotoxin (LPS)-stimulated and LPS tolerant macrophages, and to explore the role of proinflammatory and anti-inflammatory cytokines in hyporesponsive macrophages to LPS re-stimulation. Methods: In the first set of experiments,macrophages-like ceils (RAW264.7) were incubated with LPS for 0,4,8 and 20 hours. In the second set of experiments,RAW264.7 cells were pretreated with LPS for 20 hours,then the culture medium was discarded and the cells were restimulated with LPS for 4 hours. Contents of TNF-α,IL-6 and IL-10 secretions were measured in the supernatant using enzyme-linked immunosorbent assay. The expression of TNF-α and IL-10 mRNA was determined by means of semiquantitative RT-PCR. Results: Release of TNF-α,IL-6 and II.-10 was gradually increased along with LPS stimulation time. TNF-α release was reduced from LPS tolerant maerophages (pretreated with LPS for 20 hours), whereas IL-6 and IL-10 release was augmented in response to LPS restimulation. Change in TNF-α and IL-10 mRNA expression exhibited the same pattern as that of the secretion of their proteins. Conclusions: Macrophages tolerance to LPS is induced by coordinated function of proinflammatory and anti-inflammatory cytokines. When LPS-tolerized macrophages is restimulated with LPS,augmented IL-10 expression and release are the underlying mechanism of tolerance of macrophages to LPS.
出处 《感染.炎症.修复》 2012年第3期142-146,共5页 Infection Inflammation Repair
基金 国家自然科学基金资助项目(30770844)
关键词 巨噬细胞 细胞因子 内毒素 耐受 Macrophages Cytokine Endotoxin Tolerance
  • 相关文献

参考文献14

  • 1Mounoz C,Carler J,Fitting C,et al. Dysregulation of in vitro cy- tokine production by monocytes during sepsis. J Clin Invest, 1991,88:1747-1754.
  • 2Wolk HD,Thieme M, Heym S,et al. Alterations in function and phenotype of monocytes from patients with septic disease--pre- dictive value and new therapeutic strategies. Behring Inst Mitt, 1991,88:208-215.
  • 3Ertel W, Kremer J, Steckholzer U, et al. Downregulation of proinflammatory eytokine release in whole blood from septic pa- tients. Blood, 1995,85 : 1341-1347.
  • 4West MA, Heagy W. Endotoxin tolerance: a review. Crit Care Med, 2002,30 (suppl 1) : S64-S73.
  • 5Parrish WR,Gallowitsch-Puerta M, Czura CJ, et al. Experimen- tal therapeutic strategies for severe sepsis: mediators and mecha- nisms. Ann NY Acad Sci,2008,1144:210-236.
  • 6Bosshart H,Heinzelmann M. Targeting bacterial endotoxin: two sides of a coin. Ann NY Acad Sci,2007,1096:1-17.
  • 7Opal SM. The host response to endotoxin,antilipopolysaccharide strategies,and the management of severe sepsis. Int J Med Mi- crobiol, 2007,297 : 365-377.
  • 8Carroll JA,Reuter RR,Chase CC,et al. Profile of the bovine a- cute phase response following an intravenous bolus dose lipopo lysaccharide challenge. Innate Immun,2009,15:81 89.
  • 9Sanchez Lemus E, Benicky J, Pavel J, et al. In vivo angiotensin Ⅱ AT(1) receptor blockade selectively inhibits LPS-induced innate immune response and ACTH release in rat pituitary gland. Brain Behav Immun, 2009,23 : 945-957.
  • 10Cavaillon JM,Adib-Conquy M. Bench to-bedside review: endo- toxin tolerance as a model of leukocyte reprogramming in sep- sis. Crit Care, 2006,10:233.

同被引文献27

  • 1刘艳君,富宁.Toll/IL-1R家族信号转导机制研究进展[J].细胞与分子免疫学杂志,2005,21(B03):1-2. 被引量:3
  • 2Jean-Louis Mege,Soraya Meghari,Amélie Honstettre,Christian Capo,Didier Raoult.The two faces of interleukin 10 in human infectious diseases[J]. The Lancet Infectious Diseases . 2006 (9)
  • 3Andis Klegeris,Christopher J. Bissonnette,Patrick L. McGeer.Modulation of human microglia and THP-1 cell toxicity by cytokines endogenous to the nervous system[J]. Neurobiology of Aging . 2004 (5)
  • 4R.Mark Wooten,Janis J Weis.Host–pathogen interactions promoting inflammatory Lyme arthritis: use of mouse models for dissection of disease processes[J]. Current Opinion in Microbiology . 2001 (3)
  • 5Aarti Gautam,Saurabh Dixit,Mario T. Philipp.Interleukin-10 Alters Effector Functions of Multiple Genes Induced by Borrelia burgdorferi in Macrophages To Regulate Lyme Disease Inflammation. Infection and Immunity . 2011
  • 6Gautam Aarti,Dixit Saurabh,Embers Monica,Gautam Rajeev,Philipp Mario T,Singh Shree R,Morici Lisa,Dennis Vida A.Different patterns of expression and of IL-10 modulation of inflammatory mediators from macrophages of Lyme disease-resistant and -susceptible mice. PloS one . 2012
  • 7Diterich Isabel,Rauter Carolin,Kirschning Carsten J,Hartung Thomas.Borrelia burgdorferi-induced tolerance as a model of persistence via immunosuppression. Infection and Immunity . 2003
  • 8Brown Charles R,Lai Annie Y-C,Callen Steven T,Blaho Victoria A,Hughes Jennifer M,Mitchell William J.Adenoviral delivery of interleukin-10 fails to attenuate experimental Lyme disease. Infection and Immunity . 2008
  • 9Murthy P K,Dennis V A,Lasater B L,Philipp M T.Interleukin-10 modulates proinflammatory cytokines in the human monocytic cell line THP-1 stimulated with Borrelia burgdorferi lipoproteins. Infection and Immunity . 2000
  • 10Giambartolomei Guillermo H,Dennis Vida A,Lasater Barbara L,Murthy P K,Philipp Mario T.Autocrine and exocrine regulation of interleukin-10 production in THP-1 cells stimulated with Borrelia burgdorferi lipoproteins. Infection and Immunity . 2002

引证文献3

二级引证文献4

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