We investigated the role of heme oxygenase-1 (HO-1), a powerful anti-inflammatory and anti-oxidant enzyme, in modulating cigarette smoke (CS)-induced mucus secretion. In both rats and mice, 5-day CS exposure increased HO-1 expression and activity, mucus secretion, MUCIN 5AC (MUC5AC) gene and protein expression, and local inflammation, along with up-regulation of dual oxidase 1 gene expression and both the activity and phosphorylation of the epidermal growth factor receptor, which is involved in MUC5AC induction. Pharmacological induction of HO-1 prevented these actions and inhibition of HO-1 expression by a specific siRNA potentiated them. In French participants to the European Community Respiratory Health Survey II (n = 210, 30 to 53 years of age, 50% males) exposed to CS, a significant increase in the percentage of participants with chronic sputum was observed in those harboring at least one allele with a long (GT)(n) in the HO-1 promoter gene (>33 repeats), which is associated with a low level of HO-1 protein expression, compared with those with a short number of (GT)n repeats (21.7% versus 8.6%, P = 0.047). No such results were observed in those who had never smoked (n = 297). We conclude that HO-1 has a significant protective effect against airway mucus hypersecretion in animals and humans exposed to CS.

译文

:我们研究了血红素加氧酶-1(HO-1),一种强大的抗炎和抗氧化酶,在调节香烟烟雾(CS)诱导的粘液分泌中的作用。在大鼠和小鼠中,暴露5天CS均会增加HO-1的表达和活性,黏液分泌,MUCIN 5AC(MUC5AC)基因和蛋白质的表达以及局部炎症,以及双氧化酶1基因表达的上调以及两者的共同作用。参与MUC5AC诱导的表皮生长因子受体的活性和磷酸化。 HO-1的药理学诱导阻止了这些作用,并通过增强它们的特异性siRNA抑制了HO-1的表达。在参加CS的欧洲共同体呼吸健康调查II(n = 210,年龄在30至53岁,男性占50%)的法国参与者中,至少有一个患有慢性痰的参与者中,慢性痰参与者的百分比显着增加HO-1启动子基因中长(GT)(n)的等位基因(> 33个重复),与短(GT)n重复数短的等位基因相比,与HO-1蛋白表达水平低相关(21.7%对8.6%,P = 0.047)。在从未吸烟的人群中未观察到此类结果(n = 297)。我们得出的结论是,HO-1对暴露于CS的动物和人类中的气道粘液过度分泌具有显着的保护作用。

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