期刊文献+

自然杀伤细胞在屋尘螨致敏哮喘小鼠发病中的变化

The Effect of Natural Killer T Cells on the Pathogenesis of Allergic Asthma Challenged With House Dust Mite Extracts
原文传递
导出
摘要 目的探讨自然杀伤T(NKT)细胞在屋尘螨提取液(HDM)致敏哮喘小鼠发病机制中的作用。方法选择6~8周雌性无特定病原体(specific pathogen free,SPF)级BALB/C小鼠16只为研究对象,并随机分为研究组(n=8)和对照组(n=8)。研究组采用HDM致敏和激发以建立哮喘小鼠模型。对照组采用0.1mol/L磷酸盐缓冲液(PBS)替代HDM进行致敏和激发,建立小鼠模型。小鼠气道反应性测定采用肺阻抗法。支气管肺泡灌洗液(BALF)中白细胞介素(IL)-4、干扰素(IFN)-γ含量及血清总免疫球蛋白(Ig)E测定采用酶联免疫法(ELISA)。肺组织T-bet,GATA-3mRNA表达水平检测采用逆转录-聚合酶链反应(RT-PCR)法。NKT细胞及其成熟细胞比例检测采用流式细胞学技术。结果研究组小鼠气道反应性明显高于对照组,两组比较,差异有统计学意义(P<0.01)。两组小鼠BALF中细胞总数和嗜酸性粒细胞(EOC)计数比较,差异有统计学意义(P<0.01)。研究组小鼠BALF中IL-4和总IgE水平均显著高于对照组,而IFN-γ水平显著低于对照组,两组比较,差异均有统计学意义(P<0.01)。研究组小鼠T-bet mRNA水平、NKT及其成熟细胞比例明显低于对照组,而GATA-3mRNA水平显著高于对照组,两组比较,差异均有统计学意义(P<0.01)。两组小鼠NKT细胞及其成熟细胞比例与小鼠肺组织T-betmRNA表达水平呈显著正相关性关系(r=0.767,P<0.01;r=0.757,P<0.01),而与GATA-3mRNA表达水平则呈显著负相关性关系(r=-0.8871,P<0.01;r=-0.727,P<0.01)。结论 NKT细胞可能在屋尘螨致敏哮喘小鼠发病机制中起重要作用。 Objective To explore the effect of natural killer T (NKT) cells on the pathology of allergic asthma sensitized with house dust mite extracts(HDM). Methods A total, of 16 specific pathogen free (SPF) BALB/c mices were included in the study, and randomly divided into research group (n=8) and control group(n= 8). Research group was sensitized by HDM to generate the murine model of asthma. Control group was treated with phosphate buffered saline (PBS) instead of HDM. Airway hyperactivity (AHR) was analyzed by pulmonary impedance method. The level of IL-4 and IFN-'/ in bronchoalveolar lavage fluid(BALF) and the level of total IgE were detected by ELISA. The mRNA expression of T-bet and GATA-3 was measured hy RT-PCR. The number of NKT and the proportion of mature ceils were anal.yzed by flow cytometry. Results Compared to control group,AHR of research group was increased significantly (P〈0.01). The total ceils and eosinophiis (EOS) of BALF in research group were significantly higher than those of control group(P〈0.01). There had significant differences in the level of IL-4, IFN-γ and total IgE in BALF between two groups(P〈0.01). There also had significant differences in the mRNA expression of T-bet,GATA-3, the number of NKT cells and the proportion of mature cells between two groups (P% 0.01). The number of NKT cells and the proportion of mature cells had positive correlation with the expression of T-bet (r=0. 767,P〈0. 01;r=0. 757,P%0. 01),and had negative correlation with the expression of GATA-3(r=-0. 8871,P〈0.01 ;r= -0. 727 ,P%0.01L Conclusions The NKT ceils might play an important role in the pathology of murine model of asthma challenged with HDM extracts.
出处 《中华妇幼临床医学杂志(电子版)》 CAS 2013年第1期48-51,共4页 Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition)
基金 上海市科委基金资助项目(0841195310)~~
关键词 自然杀伤T细胞 哮喘 小鼠 natural killer T cells asthma mice
  • 相关文献

参考文献8

  • 1Anderson GP. Endotyping asthma: New insights into key pathogenic mechanisms in a complex, heterogeneous disease[J]. Lancet, 2008,372(9643):1107-1119.
  • 2卢燕鸣,曹兰芳.自然杀伤T细胞与支气管哮喘的研究进展[J].中华妇幼临床医学杂志(电子版),2011,7(4):305-308. 被引量:3
  • 3Ahn JH, Kim CH, Kim YH, et al. Inflammatory and remodeling events in asthma with ehronie exposure to house dust mites: A murine model[J]. J Korean Med Sci, 2007,22(6):1026-1033.
  • 4Li J, Sun B, Huang Y, et al. A multicentre study assessing the prevalence of sensitizations in patients with asthma and/or rhinitis in China[J]. Allergy, 2009,64(7) :1083-1092.
  • 5Bendelac A, Savage PB, Teyton L. The biology of NKT cells[J]. Annu Rev Immunol, 2007,25: 297-336.
  • 6Gadue P, Stein PL. NK T cell precursors exhibit differential cytokine regulation and require hk for efficient maturation[J]. J Immunol, 2002,169(5) :2397-2406.
  • 7Townsend MJ, Weinmann AS, Matsuda JL, et al. T-bet regulates the terminal maturation and homeostasis of NK and Valpha14i NKT cells[J]. Immunity, 2004,20(4) :477-494.
  • 8Matsuda JL, Zhang Q, Ndonye R, et al. T-bet concomitantly controls migration, survival, and effector functions during the development of Valpha14i NKT cells[J]. Blood, 2006, 107 (7) : 2797-2805.

二级参考文献22

  • 1Halder RC,Aguilera C, Maricic I,et al. TypeⅡ NKT cell-media- ted anergy induction in type Ⅰ NKT cells prevents inflammatory liver disease [J]. J ClinInvest, 2007, 117(8): 2302-2312.
  • 2Bendelac A, Savage P B, Teyton L. The biology of NKT cells[J]. Annu Rev Immunol, 2007,25: 297-336.
  • 3Godfrey D1, Stankovic S, Baxter AG. Raising the NKT cell family[J].Nat Immunol, 2010, 11(3):197-206.
  • 4Kronenberg M, Engel I. On the road:Progress in finding the u- nique pathway of invariant NKT cell differentiation [J]. Curr Opin Immunol, 2007, 19(2): 186- 193.
  • 5Godfrey DI, Berzins SP. Control points in NKT2 cell development [J]. Nat Revlmmunol, 2007, 7(7): 505-518.
  • 6Yu KO, Im JS, Molano A, et al. Modulation of CDla-restricted NKT cell responses by using N-acyl variants of (alphal)-galacm- sylceramides [J]. Proc NatlAead Sci USA, 2005, 102(9): 3383- 3338.
  • 7Ono 6K, Yanagawa Y, Minami K, etal. Thl or Th2 balance regu- lated by interaction between dendritic cells and NKT cells [J].Im- munol Res, 2007, 38 (1-3): 319 332.
  • 8Akbari O, Stock P, Meyer E, et al. Essential role of NKT cells producing 1L-4 and IL-13 in the development of allergn-induced air- way hyperreactivity[J]. Nat Med, 2003, 9(5): 582-588.
  • 9Meyer EH, Goya S, Akbari O, et al. Glycolipid activation of in- variant T cell receptor + NKT ceils is su{ficient to induce airway hyperreactivity independent of conventional CD4 + T cells [J]. Proc Natl Acad Sci USA, 2006, 103(8): 2782-2787.
  • 10Pichavant M, Goya S, Meyer EH, et al. Ozone exposure in a mouse model induces airway hyperreactivity that requires the pres- ence of natural killer T cells and IL-17 [J]. J Exp Med, 2008, 205(2): 385-393.

共引文献2

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