摘要
目的探讨白介素13受体α2(IL-13Rα2)与气道重塑的的关系。方法用OVA腹腔注射致敏SPF级BALB/c小鼠,雾化吸入激发制作哮喘模型,同时予地塞米松腹腔注射干预,最后一次致敏后24 h处死小鼠,观察并测量肺组织形态学改变,用RT-PCR和免疫组化法分别检测小鼠肺组织中IL-13Rα2 mRNA和蛋白的表达及TGF-β1 mRNA表达。结果哮喘小鼠与对照组、地塞米松组小鼠比较,支气管管壁(17.58±0.78)vs.(12.61±0.87)vs.(13.89±0.94)、平滑肌面积(6.71±0.83)vs.(4.61±0.46)vs.(5.62±0.53)均明显增加,P<0.01,RT-PCR发现肺组织中IL-13Rα2 mRNA(0.670±0.183)vs.(0.075±0.058)vs.(0.262±0.138)和TGF-β1 mRNA(0.704±0.168)vs.(0.317±0.140)vs.(0.358±0.098)明显增高,P<0.01,免疫组化发现IL-13Rα2蛋白表达(52.11±6.30)vs.(17.80±4.09)vs.(22.87±3.76)明显增高,P<0.01。结论 IL-13Rα2在哮喘小鼠肺组织表达增加,与气道重塑密切相关。
Objective To investigate the relationship between interleukin-13 receptor α2(IL-13Rα2) and airway remodeling. Methods SPF level BALB/c mice were injected with OVA intraperitoneal by sensitization, and inhalation stimulation, and dexamethasone intervention by intraperitoneal injection. Mice were sacrificed 24 h after the last sensitization. It was observed that morphological changes in mice lung tissue. IL-13 Rαt2 mRNA , TGF-β1 mRNA and IL-13 Rα2 protein expression in mice lung tissues were detected by reverse transcription-polymerase chain reaction (RT-PCR) and immunohistochemisty respectively. Results Compared with the control group, dexamethasone group, the bronchial wall of asthmatic mice became thicker ( 17.58 ± 0.78) vs. ( 12.61± 0.87) vs. ( 13.89 ±0.94), P 〈 0.01, and their smooth muscle area was much thicker too (6.71 ±0.83) vs. (4.61 ±0.46) vs. (5.62 ±0.53), P 〈0.01. RT-PCR found that IL-13R α2 mRNA (0. 670 ± 0. 183 ) vs. (0. 075 ± O. 058 ) vs. (0. 262±0. 138 ) and TGF-β1 mRNA (0. 704 ± 0. 168) vs. (0. 317 ± 0.140) vs. (0. 358 ± 0. 098) significantly increased in lung tissue, P 〈 0. 01, and immunohistochemistry showed that IL-13Rα 2 protein expression (52. 11 ± 6.30) vs. ( 17.80 ± 4.09) vs. ( 22.87 ±3.76 ) was evidently higher, P 〈 0.01. Conclusion The expression of IL-13 Rα2 in asthmatic mice lung tissue is increased, which has close relationship with airway remodeling.
出处
《中华肺部疾病杂志(电子版)》
CAS
2015年第1期30-33,共4页
Chinese Journal of Lung Diseases(Electronic Edition)
基金
国家自然科学基金青年科学基金项目(81302016)