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作 者:莫冠文[1] 蔡绍曦[1] 赵海金[1] 李文军[2] 佟万成[1] 刘来昱[1]
机构地区:[1]南方医科大学南方医院呼吸科,广东广州510515 [2]南方医科大学公共卫生与热带医学学院,广东广州510515
出 处:《南方医科大学学报》2011年第2期239-243,共5页Journal of Southern Medical University
基 金:国家自然科学基金(30270593);中华医学会慢性呼吸道疾病专项基金(07010130021;08020460124);广东省科技计划基金(2005207007)~~
摘 要:目的探讨甲苯二异氰酸盐(TDI)对正常人支气管上皮细胞(16HBE)活性氧(ROS)生成及通透性的影响。方法应用改良的Son氏等方法制备TDI-人血清白蛋白(TDI-HSA)。四唑盐(MTT)比色法检测不同浓度的TDI-HSA对正常人支气管上皮细胞株16HBE活力的影响。实验分4组:以未加任何处理因素的16HBE为对照组,20、60、100μg/ml的TDI-HSA处理16HBE 24 h,通过2',7'-二氢二氯荧光黄双乙酸钠(DCFH-DA)细胞内ROS荧光染色,收集细胞后以流式细胞仪检测荧光强度。选择对ROS水平影响较大的100μg/ml的TDI-HSA处理16HBE 24 h。流式细胞仪定量检测抗氧化剂N-乙酰半胱氨酸(NAC)对TDI-HSA诱导ROS生成的影响,荧光显微镜观察照相。采用跨上皮电阻(TEER)法检测上皮单层细胞的通透性。结果 120μg/ml以下浓度的TDI-HSA对细胞活力无显著影响。ROS水平在对照组、20、60和100μg/ml组分别为:65.04±4.56,91.76±4.84,119.96±10.40,203.11±8.21。100μg/ml TDI-HSA组与对照组及20、60μg/ml组相比,16HBE的ROS水平显著升高(P<0.05)。对照组、100μg/ml TDI-HSA处理组、50 mmol/L NAC预处理组的细胞内ROS水平分别为:69.02±2.14,246.47±18.55,102.50±4.60;而TEER分别为:280.75±11.93,92.25±11.44,207.25±7.41。NAC可显著降低TDI-HSA诱导的ROS生成(P<0.05),改善氧化应激对单层细胞通透性的影响(P<0.05)。结论 TDI显著增加HBEROS的产生,其诱导的氧化应激部分参与支气管上皮细胞通透性的增加。这可能是TDI诱发哮喘的发病机制之一。Objective To investigate the effect of toluene diisocyanate(TDI) on the production of reactive oxygen species(ROS) and the permeability of human bronchial epithelial(HBE) cells.Methods TDI-human serum albumin(TDI-HSA) conjugate was prepared using a modified Son's method.MTT assay was used to assess HBE cell viability after exposure to different concentrations of TDI-HSA.The level of intracellular ROS of HBE cells was detected by flow cytometry with an oxidation-sensitive fluorescent probe 2',7'-dichlorofluorescein diacetate(DCFH-DA) uploading,and the permeability of cell monolayer was assessed by detecting the transepithelial electrical resistance(TEER).Results The exposure to 120 μg/ml TDI-HSA did not obviously affect the cell viability.Compared with the control group,the intracellular fluorescent intensity increased significantly in the cells exposed to 20,60,and 100 μg/ml TDI-HSA(P0.05).The intracellular ROS production increased significantly after 100 μg/ml TDI-HSA treatment(P0.05),but the increment in ROS production was significantly suppressed by pretreatment of the cells with N-acetylcysteine(NAC)(P0.05),which also enhanced the TEER decreased by TDI-HSA treatment(P0.05).Conclusion TDI enhances the permeability of HBE cell monolayer partially through a ROS-mediated pathway,suggesting the importance of oxidative stress in TDI-induced pulmonary diseases.
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