期刊文献+

IL-17在哮喘小鼠模型中表达及其对肥大细胞IL-6分泌的影响 被引量:4

Expression of IL-17 in asthmatic mice and its eftect on release of IL-6 in mast cells
下载PDF
导出
摘要 目的 :研究白细胞介素(interleukin,IL)-17在哮喘小鼠模型中的表达,观察其对肥大细胞IL-6分泌的影响。方法:BALB/c小鼠随机分为对照组和哮喘组,分别用等量磷酸盐缓冲液(phosphate buffer solution,PBS)和卵清蛋白(ovalbumin,OVA)干预,检测肺泡灌洗液(bronchoalveolar lavage fluid,BALF)中细胞总数及嗜酸性粒细胞(eosnophils,EOS)数验证模型的成功建立。应用逆转录-聚合酶链反应法、酶联免疫吸附实验(enzyme-linked immunosorbent assay,ELISA)检测两组小鼠肺组织中IL-17m RNA、BALF及血清中IL-17的表达差异。细胞实验分为对照组和IL-17组,分别予等量培养基和IL-17干预小鼠肥大细胞株(P815)后收集上清,用ELISA检测IL-6的水平。结果 :哮喘组BALF中细胞总数及EOS计数较对照组显著升高(P<0.05),模型建立成功。哮喘组肺组织中IL-17 m RNA、BALF及血清中IL-17表达较正常组显著升高(P<0.05)。细胞水平的研究发现IL-17组P815上清中IL-6表达较正常组显著升高(P<0.05)。结论 :IL-17在OVA诱导哮喘小鼠模型中表达升高。IL-17刺激肥大细胞分泌IL-6,可能在哮喘的发病中起促进作用。 Objective:To observe the expression of interleukin(IL)-17 in asthmatic mice and to investigate the effect of IL-17 on release of IL-6 in mast cells. Methods:BALB/c mice were randomly divided into control group and asthma group,and treated with equal amount of phosphate buffer solution(PBS)and ovalbumin(OVA),respectively. Mouse asthma model was validated by detecting the total number of cells and cosinophils(EOS)in bronchoalveolar lavage fluid(BALF). The expression differences between IL-17 mRNA in lung tissues and IL-17 in BALF and serum were measured by reverse transcription-polymerase chain reaction(RT-PCR)and enzyme-linked immunosorbent assay(ELISA)in the two groups. Mouse P815 mast cells were divided into the control group and the IL- l7 group, and treated with equal amount of culture medium and IL-17, respectively. The levels of released IL-6 in supernatants were detected by ELISA. Results:In BALF,the total number of cells and EOS in the asthma group were significantly increased than those in the control group(P 〈 0.05),and the model was validated. The expressions of IL-17 mRNA in lung tissues and IL-17 in BALF and serum were significantly increased in the asthma group than those in the control group (P 〈 0.05). In P815 cell supernatants,the secretion of IL-6 in the IL-17 group was significantly increased than that in the control group(P 〈 0.05). Conclusion:The expression of IL-17 was increased in OVA-induced mouse asthma model. IL-17 may promote the process of asthma by stimulating IL-6 release by mast cells.
出处 《南京医科大学学报(自然科学版)》 CAS CSCD 北大核心 2015年第3期363-366,共4页 Journal of Nanjing Medical University(Natural Sciences)
基金 国家自然科学基金青年项目(81200012) 南京市医学科技发展项目(201108012)
关键词 白细胞介素-17 哮喘 小鼠 肥大细胞 白细胞介素-6 IL-17 asthma mouse mast cell IL-6
  • 相关文献

参考文献16

  • 1Boulet LP, Fitzgerald JM,Levy ML,et al. A guide to the translation of the Global Initiative for Asthma (GINA) strategy into improved care[J]. Eur Respir J,2012,39 (5) : 1220-1229.
  • 2Holt PG,Strickland DH. Interactions between innate and adaptive immunity in asthma pathogenesis:new perspec- tives from studies on acute exacerbations[J]. J Allergy Clin Immunol, 2010, 125 (5) : 963-974.
  • 3Kumar RK,Yang M,Herbert C,et al. Interferon-gamma, pulmonary macrophages and airway responsiveness in asthma [J]. Inflamm Allergy Drug Targets,2012,11 (4): 292-297.
  • 4Harrington LE, Hatton RD, Mangan PR, et al. Interleukin 17-producing CD4+ effeetor T cells develop via a lineage distinct from the T helper type 1 and 2 lineages [J]. Nat Immunol, 2005,6 ( 11 ) : 1123-1132.
  • 5Onishi RM,Gaffen SL. Interleukin-17 and its target genes: mechanisms of interleukin-17 function in disease[J]. Im- munology, 2010,129 (3) : 311-321.
  • 6Zhao Y,Yang J,Gao YD,et al. Thl7 immunity in patients with allergic asthma[J], lnt Arch Allergy Immunol, 2010, 151(4) :297-307.
  • 7Bradding P. The role of the mast cell in asthma: a re- assessment[J]. Curr Opin Allergy Clin Immunol,2003,3 ( 1 ) :45-50.
  • 8Qin HB,Xu B,Mei JJ,et al. Inhibition of miRNA-221 suppresses the airway inflammation in asthma[J]. Inflam- mation, 2012,35 (4) : 1595-1599.
  • 9Xu G,Zhang L,Wang DY,et al. Opposing roles of IL-17A and IL-25 in the regulation of TSLP production in human nasal epithelial cells[J]. Allergy,2010,65(5) :581-589.
  • 10许长娣,梅娟娟,李丹,刘娟娟,秦厚兵,刘峰,赵德育.microRNA在卵清蛋白诱导的支气管哮喘小鼠模型中的表达[J].实用儿科临床杂志,2012,27(21):1655-1657. 被引量:5

二级参考文献15

  • 1Masoli M,Fabian D,Holt S,et al. The global burden of asthma:Execu-tive summary of the GINA Dissemination Committee report [ J]. Allergy,2004,59(5).:469 -478.
  • 2van Rooij E,Purcell AL,Levin AA. Developing microRNA therapeutics[J]. Circ i.e5,2012,110(3). :496 -507.
  • 3Chiba Y,Misawa M. MicroRNAs and their therapeutic potential for hu-man diseases: MiR - 133a and bronchial smooth muscle hyperrespon-siveness in asthma[ J]. J Pharmacol ,2010,114(3). :264 -268.
  • 4Liston A,Linterman M,Lu LF. MicroRNA in the adaptive immune sys-tem ,in sickness and in health[ J]. J Clin Immunol,2010,30(3). :339 -346.
  • 5Wang Z, Li Y, Kong D,et al. Cross - talk between miRNA and Notchsignaling pathways in tumor development and progression [ J]. CancerLett,2010 f292(2). :141 -148.
  • 6Gracias DT,Katsikis PD. MicroRNAs:Key components of immune regu-lation [J]. Adv Exp Med Biol y20l 1,780 : 15 -26.
  • 7Mohamed JS, Lopez MA, Boriek AM. Mechanical stretch up - regulatesmicroRNA -26 a and induces human airway smooth muscle hypertrophyby suppressing glycogen synthase kinase - 3p [ J]. J Biol Chem,20J0,285(38).:29336 -29347.
  • 8Mattes J, Collison A,Plank M, et al. Antagonism of microRNA - 126suppresses the effector function of TH2 cells and the development of al-lergic airways disease [ J]. Proc Natl Acad Sci U S A ,2009 ,106 (44).;18704 -18709.
  • 9Polikepahad S,Knight JM,Naghavi A0,et al. Proinflammatory role forlet -7 microRNAS in experimental asthma[ J]. l Biol Chemf20J0 t2S5(39). :30139 -30149.
  • 10Morales JK,Falanga YT,Depcrynski A,et al. Mast cell homeostasis andthe JAK - STAT pathway [ J]. Genes Immun ,2010 J (8). :599 -608.

共引文献4

同被引文献43

引证文献4

二级引证文献33

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