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机构地区:[1]山西大学环境医学与毒理学研究所环境毒理学研究室,太原030006
出 处:《中国公共卫生》2007年第12期1457-1459,共3页Chinese Journal of Public Health
基 金:国家自然科学基金(20677035)
摘 要:目的研究二氧化硫(SO2)衍生物染毒后人支气管上皮细胞(BEP2D)哮喘相关基因黏蛋白5AC(MUC5AC)和白介素-13(IL-13)表达的变化。方法以不同浓度SO2衍生物(0.000 1,0.001,0.01,0.1,1 mmol/L)对BEP2D细胞染毒,采用荧光实时定量RT-PCR、免疫细胞化学和酶联免疫吸附法(ELISA)等方法测定基因的表达。结果不同浓度SO2衍生物处理的BEP2D细胞中MUC5AC和IL-13 mRNA和蛋白表达比对照组明显增加;经0.1 mmol/L SO2衍生物处理后换新鲜培养基再孵育不同的时间,MUC5AC和IL-13 mRNA水平均显著增高,在更换新鲜培养基孵育4 h时达到峰值,24 h时虽然有所降低,但仍比对照组显著增高。结论SO2衍生物能增加EBP2D细胞MUC5AC和IL-13在转录和翻译水平上的表达,提示这可能是SO2加重哮喘疾病的原因之一。Objective To explore the effects of SO2 derivatives on MUC5AC and IL - 13 gene expressions in the human bronchial epithelial cells(BEP2D). Methods Using BEP2D cells, the mRNA and protein levels of MUC5AC and IL - 13 gene at different concentrations of SO2 derivatives(0.000 1,0. 001,0.1, 1 mmol/L) were measured by real - time RT - PCR technology and immunocytochemistry method, respectively. Results Different concentrations of SO2 derivatives exposure (0. 000 1,0.001,0.01, 0.1, 1 mmol/L) amd different post- exposure time(0.1 mmol/L SO2 derivatives) at 0, 5, 1, 4 and 24 h increased mRNA expressions of MUC5AC and IL - 13 in BEP2D cells compared with the control. Meanwhile, MUC5AC and IL - 13 protein levels in BEP2D cells were increased at different concentrations of SO2 derivatives exposure and different post - exposure time, peaking in 4 h post - exposure and increasing in 24 h post - exposure compared with the control. Conclusion SO2 derivatives exposure could increase the expressions of MUC5AC and IL - 13 genes on the transcription and translation levels in BEP2D cells, suggesting it might be one of the possible reasons that SO2 pollution aggravates asthma disease.
关 键 词:SO2衍生物 哮喘 黏蛋白(mucin MUC)5AC(MUC5AC) 白介素-13(IL-13) 人支气管上皮细胞(BEP2D)
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