期刊文献+

黄芪和地塞米松对哮喘失衡表达转录因子T—bet/GATA-3不同的调节作用 被引量:2

Different regulatory effect of Astragalus membranaceus and dexamethasone on imbalanced T cell-specific transcription factors T-bet and GATA-3 in asthma
原文传递
导出
摘要 目的观察T细胞特异转录因子T—bet/GATA-3在支气管哮喘中失衡表达,探讨黄芪和地塞米松对其不同的调节作用。方法40只雄性SPF级SD大鼠随机分为对照组、哮喘组、地塞米松组和黄芪组,20只雄性SPF级致敏SD大鼠脾脏中分离获得CD4^+T细胞,苏木精-伊红染色观察气道病理改变;酶联免疫吸附试验(ELISA)检测大鼠血清中IL-4、IL-5、IFN-γ含量;逆转录-聚合酶链反应(RT-PCR)检测IL-4、IL-5、IFN-γ、T—bet和GATA-3mRNA表达;Western blot法检测T—bet和GATA-3蛋白表达。结果肺组织中嗜酸粒细胞(EOS)、淋巴细胞、管壁面秽支气管管腔内周长(WA/Pi)和支气管平滑肌面积/支气管管腔内周长(ASM/Pi)哮喘组比对照组明显增多或增厚(P均〈0.01),地塞米松组和黄芪组明显低于哮喘组(P均〈0.01);血清中IL-4和IL-5含量,哮喘组高于对照组(P均〈0.01),地塞米松组和黄芪组均低于哮喘组(P均〈0.01),血清中IFN-γ含量哮喘组远低于对照组(P〈0.01),地塞米松组低于对照组(P〈0.01),但黄芪组明显高于哮喘组(P〈0.01)。在大鼠肺组织和致敏大鼠脾CD4^+T细胞中,IFN-γ mRNA、T-bet mRNA和蛋白表达哮喘组明显低于对照组(P均〈0.01),地塞米松组与哮喘组相似(P〉0.05),黄芪组与对照组相似,但明显高于哮喘组(P〈0.01);IL4和IL-5mRNA、GATA-3mRNA和蛋白表达,哮喘组异常高于对照组(P〈0.01),地塞米松组和黄芪组均明显低于哮喘组(P〈0.01);肺组织中T—bet/GATA-3蛋白表达量比值,哮喘组明显低于对照组(P〈0.01),地塞米松组与哮喘组相近(P〉0.05),黄芪组与对照组的比值相近(P〉0.05),明显高于哮喘组和地塞米松组(P均〈0.01)。结论T细胞特异转录因子T—bet/GATA-3在哮喘中失衡表达,黄芪抑制哮喘气道炎症可能通过双向调� Objective To investigate imbalanced T cell-specific transcription factors T-bet and GATA-3 in asthmatic rats, and to identify the different effects of astragalus and dexamethasone on them. Methods Forty male SD rats were randomly divided into a control group, an asthmatic group, a dexamethasone group, and an astragalus group, and were observed the change of airway histology. Two weeks after immunization, CD4^+ T cells were obtained from singled-cell suspension of spleen (after lysis of RBCs). The concentrations of IL-4, IL-5, IFN-γ in serum were measured by ELISA. The mRNA expressions of IL-4, IL-5, IFN-γ, T-bet and GATA-3 in the lungs and CD4 ^+ T cells were detected by RT-PCR, and the protein expressions of T-bet and GATA-3 in the lungs and CD4^+ T cells were detected by Western blot respectively. Results In the asthmatic group, the numbers of eosinophils and lymphocytes, the thicknesses of WA/Pi and ASM/Pi were (25.70 ± 2.50)/mm^2, (44.80 ± 5.69 )/mm^2, ( 12. 15 ± 1.47 ) mm, (6.82 ± 0.91 ) mm, and those of the control group were (2.40 ± 1.27 )/mm^2, (8.90 ± 1.97)/mm^2, (6.49 ±1.57) mm, (2.75 ±0. 62) mm, and those of the dexamethasone group were (6.70 ± 1. 89)/mm^2, (15. 80± 3.12) /mm^2, (8.02±1.35)mm, (3.38±0.65)mm, and those of the astragalus group were (11.20 ± 2.97)/mm^2 , ( 19.80 ± 4.59) /mm^2, ( 8.86 ± 0.96) mm, ( 3.96 ± 0. 61 ) mm. There were significant differences between the asthmatic group and the control group, the asthmatic group and the dexamethasone group, and the astragalus group ( P 〈 0.01 ). In the asthmatic group, the concentrations of IL-4, IL-5, IFN- γ in serum were (35.23 ±8.02) pg/ml, (32.03 ±3.99) pg/ml, ( 16.73 ±5.15) pg/ml, and those of the control group were ( 14.48 ± 1.68 ) pg/ml, ( 14.23 ± 0.97 ) pg/ml, (64.55 ± 14.04) pg/ml, and those of the dexamethasone group were ( 14.97±1.09) pg/ml, ( 16.13 ±2.36) pg/ml, ( 16.69 ± 4.05 ) pg/ml, those of
出处 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 2009年第10期907-913,共7页 Chinese Journal of Microbiology and Immunology
关键词 哮喘 转录因子 T淋巴细胞 黄芪 地塞米松 Asthma Transcription factors T lymphocyte Astragalus membranaceus Dexamethasone
  • 相关文献

参考文献12

  • 1卞涛,殷凯生,金淑贤,孟自力,周锦勇,马秀琴,胡静静,德伟.支气管哮喘大鼠转录因子T-bet/GATA-3失衡表达与气道炎症的关系[J].中华结核和呼吸杂志,2006,29(3):176-180. 被引量:29
  • 2Chakir H,Wang H,Lefebwe DE,et al.T-bet/GATA-3 ratio as a measure of the Th1/Th2 cytokine profile in mixed cell population:predominant role of GATA-3.J Immunol Methods,2003,278(1-2):157-169. 被引量:1
  • 3Meyer EH,Dekruff RH,Umetsu DT.T cells and NKT cells in the pathogenesis of asthma.Annu Rey Med,2008,59(18):281-292. 被引量:1
  • 4Wegmann M.Th2 cells aa tagets for therapeutic intervention in allergic bronchial asthma.Expert Rev Mol Diagn,2009,9(1):85-100. 被引量:1
  • 5Szabo SJ,Kim ST,Costa GL,et al.A novel transcription factor,T-bet,directs Th1 lineage commitment.Cell,2000,100(6):655-669. 被引量:1
  • 6Amsen D,Antov A,Jankovic D,et al.Direct regulation of Gata3 expression determines the T helper differentiation potential of Notch.Immunity,2007,27(1):89-99. 被引量:1
  • 7Finotto S,Neurath MF,Glickman JN,et al.Development of spontaneous airway changes consistent with human asthma in mice lacking T-bet.Science,2002,295(11):336-338. 被引量:1
  • 8Park JW,Min HJ,Sohn JH,et al.Restoration of T-box-containing protein expressed in T cells expression in T cells protects aeainst allergen-induced asthma.J Allergy Clin Immunol,2009,123(2):479-485. 被引量:1
  • 9Lee CC,Huang HY,Chiang BL.Lentiviral-mediated GATA-3 RNAi decreases allergic airway inflanunation and hyperresponsiveness.Mol Ther,2008,16(1):60-65. 被引量:1
  • 10Lighvani AA,Frueht DM,Jankovic D,et al.T-bet is rapidly induced by interferon--gamma in lymphoid and myeloid cells.Proc Nad Acad Sci USA,2001,98(26):15137-15142. 被引量:1

二级参考文献26

  • 1王德昌,李秀如.黄芪多糖Fb对人血淋巴细胞免疫功能的影响[J].中华肿瘤杂志,1989,11(3):180-183. 被引量:21
  • 2汤颖,娄探奇,成彩联,彭晖,关伟明.实验性IgA肾病模型的改进[J].中山大学学报(医学科学版),2006,27(2):184-187. 被引量:110
  • 3蔡小燕,许艳丽,林小军,傅君舟,秦曙光,李剑文.黄芪注射液对系统性红斑狼疮患者细胞凋亡和免疫功能的影响[J].中国中西医结合杂志,2006,26(5):443-445. 被引量:26
  • 4Hsu SI, Ramirez SB, Winn MP, et al. Evidence for genetic factors in the development and progression of IgA nephropathy. Kidney Int, 2000,57 : 1818-1835. 被引量:1
  • 5Woodroffe AJ, Gormly AA, Clarkson AR. Experimental cirrhosis and deposition of glomerular IgA immune complexes. Contrid Nephrol, 1984, 40:51-54. 被引量:1
  • 6Hsu SI, Ramirez SB ,Winn MP, et al. Evidence for genetic factors in the development and progression of IgA nephropathy. Kidney Int ,2000,57 : 1818-1835. 被引量:1
  • 7Ebihara I, Hirayama K, Yamamoto S, et al. Th2 predominance at the single-cell level in patients with IgAnephropathy. Nephrol Dial Transplant,2001,16 : 1783-1789. 被引量:1
  • 8Kjerruf M, Gdic D, Kopf M, et al. Induction of gut mucosal immune rerponses: importance of genetic background and Th1/ Th2 cross regulation. Seand J Immunal, 1998,47:401-407. 被引量:1
  • 9Ballardie FW, Gordon MT, Sharpe PT, et al. Intrarenal cytokine mRNA expression and location in normal and IgA nephropathy tissue: TGF , TGF, IGF-1, IL-4 and IL-6. Nephrol Dial Transplant, 1994,9 : 1545-1552. 被引量:1
  • 10Schena FP, Gesualdo L, Grandaliano G, et al. Progression of renal damage in human glomerulonephritides: Is there sleight of hand in winning the game. Kidney Int, 1997, 52 : 1439-1457. 被引量:1

共引文献37

同被引文献15

  • 1Haldar P, Brightling CE, Hargadon B, Gupta S, Monteiro W, Sousa A, et al. Mepolizumab and exacerbations of refractory eosinophilic asthma[J]. N Engl J Med, 2009, 360(10) : 973-984. 被引量:1
  • 2Bao Z, Guan S, Cheng C, Wu S, Wong SH, Kemeny DM, et al. A novel antiiuflammatory role for andrographolide in asthma via inhibition of the nuclear faetor-kappaB pathway [ J ]. Am J Respir Crit Care Med, 2009, 179(8) : 657-665. 被引量:1
  • 3Park S J, Lee KS, Kim SR, Min KH, Choe YH, Moon H, et al. Peroxisome proliferator-activated receptor gamma agonist down-regulates IL-17 expression in a murine model of allergic airway inflammation [ J ]. J Immunol, 2009, 183 (5) : 3259-3267. 被引量:1
  • 4Huang JJ, Joh JW, Fuentebella J, Patel A, Nguyen T, Seki S, et al. Eotaxin and FGF enhance signaling through an extracellular signal-related kinase (ERK) -dependent pathway in the pathogenesis of eosinophilic esophagitis [ J ]. Allergy Asthma Clin hnmunol, 2010, 6(1): 25. 被引量:1
  • 5Barnes PJ. New therapies for asthma: is there any progress? [ J ]. Trends Pharmacol Sci, 2010, 31(7): 335-343. 被引量:1
  • 6Hamid Q, Tulic M. Immunobiology of asthma [ J ]. Annu Rev Physiol, 2009, 71: 489-507. 被引量:1
  • 7Queto T, Gaspar-Elsas MI, Masid-de-Brito D, Vasconcelos ZF, Ferraris FK, Penido C, ct al. Cysteinyl-leukotriene type 1 receptors transduce a critical signal for the up-regulation of eosinophilopoiesis by interleukin-13 and eotaxin in murine bone marrow [ J ]. J Leukoc Biol, 2010, 87(5) : 885-893. 被引量:1
  • 8Abu-Ghefreh AA, Canatan H, Ezeamuzie CI. In vitro and in vivo anti-inflammatory effects of andrographolide [ J ]. Int Immunopharmacol, 2009, 9(3): 313-318. 被引量:1
  • 9Chandrasekaran CV, Gupta A, Agarwal A. Effect of an extract of Andrographis paniculata leaves on inflammatory and allergic mediators in vitro [ J ]. J Ethnopharmacol, 2010, 129 (2) : 203-207. 被引量:1
  • 10Dougherty RH, Fahy JV. Acute exacerbations of asthma : epidemiology, biologyand the exacerbation-prone phenotype[ J]. Clin Exp Allergy, 2009, 39(2) : 193-202. 被引量:1

引证文献2

二级引证文献13

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