机构地区:[1]南京医科大学第一附属医院呼吸科,210029 [2]南京医科大学生化实验室
出 处:《中华结核和呼吸杂志》2006年第3期176-180,共5页Chinese Journal of Tuberculosis and Respiratory Diseases
摘 要:目的探讨支气管哮喘(简称哮喘)转录因子T-bet/GATA-3表达量比值的变化及其与气道炎症的关系。方法24只雄性SD大鼠按随机数字表法分为对照组、哮喘组,每组12只。用动物肺功能仪测定大鼠气道反应性;用苏木精-伊红染色观察气道病理改变;用酶联免疫吸附测定(ELISA)法检测大鼠支气管肺泡灌洗液(BALF)中白细胞介素4(IL-4)、IL-5、γ干扰素(IFN-γ)含量;用逆转录-聚合酶链反应(RT-PCR)测定法检测肺组织中IL-4、IL-5、IFNγ-、T-bet和GATA-3 mRNA的表达水平;用免疫印迹(W estern b lot)法检测肺组织T-bet和GATA-3蛋白的表达水平。结果用同等剂量氯化乙酰胆碱(20、40、80、160μg/m l)激发时平均呼气阻力哮喘组分别为(6.26±0.85)、(11.55±3.09)、(28.74±5.94)、(3 710.83±197.49)cm H2O.m l-1.s-1,对照组分别为(1.51±0.18)、(2.15±0.36)、(6.08±1.06)、(37.17±6.12)cm H2O.m l-1.s-1,两组不同激素剂量比较差异有统计学意义(P均<0.01);肺组织中嗜酸粒细胞(EOS)、淋巴细胞数,管壁面积/支气管管腔内周长(WA/P i)和支气管平滑肌面积/支气管管腔内周长(ASM/P i)哮喘组分别为(26.0±1.6)个/mm2、(45.2±3.2)个/mm2、12.0±1.4、6.7±0.6,对照组分别为(2.9±1.2)个/mm2、(8.8±1.8)个/mm2、6.4±0.8、2.7±0.5,两组比较差异有统计学意义(P均<0.01);BALF中IL-4、IL-5和IFN-γ含量哮喘组为(23.4±0.7)pg/m l、(24.8±0.5)pg/m l和(21.7±1.1)pg/m l,对照组为(9.3±0.3)pg/m l、(12.5±0.3)pg/m l、(65.8±2.1)pg/m l,两组比较差异有统计学意义(P均<0.01);肺组织中IL-4、IL-5和IFN-γmRNA表达水平哮喘组分别为2.260±0.210、0.510±0.100、0.100±0.020,对照组分别为0.060±0.020、0.160±0.020、0.850±0.260,两组比较差异有统计学意义(P均<0.01)。肺组织中T-bet/GATA-3 mRNA表达量比值对照组为0.73±0.32,哮喘组为0.06±0.09,两组比较差异有统计学意义(P<0.01);肺组织中T-bet/GATA-3蛋白表达量比值哮喘组为0.09±0.04,对照组为0.75±0.25,两组Objective To identify the change of the mRNA and protein expression of T-bet and GATA-3 in lung tissues, and to investigate the association between the imbalanced T cell-specific transcription factors Tobet/GATA-3 and the airway inflammation in asthmatic rats. Methods Twenty-four male SD rats were randomly divided into a control group and an asthmatic group. Airway responsiveness was measured and the change of airway histology was observed. The concentrations of interleukin-4 (IL-4), IL-5 ,and interferon-γ (IFN-γ) in bronchoalveolar lavage fluid (BALF) were measured by enzyme-linked immunosorbent assay (ELISA). The mRNA and protein expressions of IL-4, IL-5, IFN-γ, T-bet and GATA-3 in the lungs were detected by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot respectively. Results The expiration resistance after injection of acetylcholine chloride (20, 40, 80, 160 μg/ml) in the asthmatic group was (6.26 ±0.85), (11.55 ±3.09), (28.74 ±5.94), (3 710. 83 ± 197.49)cm H2O·ml^-1· s^-1 respectively; and that in the control group was ( 1.51 ±0. 18), (2. 15 ±0. 36), (6.08 ± 1.06), (37. 17 ±6. 12)cm H2O·ml^-1 · s^-1 respectively; the difference being significant between the two groups (all P 〈0.01 ). In the asthmatic group, the numbers of eosinophils and lymphocytes, the thicknesses of WA/Pi and ASM/Pi were ( 26.0 ± 1.6 )/mm^2, ( 45.2 ± 3. 2 )/mm^2, 12.0±1.4, 6.7 ±0.6, respectively; and those of the control group were (2.9 ± 1.2)/mm^2, (8.8 ± 1.8)/mm^2 ,6.4 ±0. 8,2. 7 ±0. 5, respectively; all were significantly different between the two groups ( all P 〈0. 01). In the asthmatic group, the concentrations of IL-4, IL-5, and IFN-γ in BALF were (23.4 ±0. 7) pg/ml, (24. 8 ± 0. 5 ) pg/ml, (21.7 ± 1.1 ) pg/ml, respectively, and those of the control group were (9. 3 ± 0. 3) pg/ml, ( 12. 5 ± 0. 3 ) pg/ml, (65. 8 ± 2. 1 ) pg/ml, respectively; all were significantly differ
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