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自分泌 TGF-α与苯并(a)芘诱导的变应性哮喘中黏液产生和 MUC5AC 表达有关。

Autocrine TGF-alpha is associated with Benzo(a)pyrene-induced mucus production and MUC5AC expression during allergic asthma.

机构信息

Department of Pulmonary Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.

Department of Respiratory Medicine, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200062, PR China.

出版信息

Ecotoxicol Environ Saf. 2022 Aug;241:113833. doi: 10.1016/j.ecoenv.2022.113833. Epub 2022 Jul 4.

Abstract

OBJECTS

Benzo(a)pyrene (BaP), an environmental pollutant, is present in high concentrations in urban smog and cigarette smoke and has been reported to promote high mucin 5AC (MUC5AC) expression. Epithelium-derived inflammatory cytokines are considered an important modulator of mucus oversecretion and MUC5AC overexpression. Here, we investigated whether the effect of BaP on MUC5AC overexpression was associated with cytokine autocrine activity in vivo and in vitro.

METHODS

In vivo, BALB/c mice were treated with ovalbumin (OVA) in the presence or absence of BaP. Allergy-induced mucus production was assessed by Alcian Blue Periodic acid Schiff (AB-PAS) staining. The human airway epithelial cell line NCI-H292 was used in vitro. MUC5AC and transforming growth factor (TGF)-α mRNA levels were assessed with real-time quantitative PCR. The concentration of cytokines was measured by ELISA. The MUC5AC, p-ERK, ERK, p-EGFR and EGFR proteins were detected by Western blotting in cells or by immunohistochemistry in mouse lungs. Small-interfering RNAs were used for gene silencing.

RESULTS

TGF-α was overproduced in the supernatant of NCI-H292 cells treated with BaP. Knockdown of TGF-α expression inhibited the BaP-induced increase in MUC5AC expression and subsequent activation of the EGFR-ERK signalling pathway. Knocking down aryl hydrocarbon receptor (AhR) expression or treatment with an ROS inhibitor (N-acetyl-L-cysteine) could relieve the TGF-α secretion induced by BaP in epithelial cells. In an animal study, coexposure to BaP with OVA increased mucus production, MUC5AC expression and ROS-EGFR-ERK activation in the lung as well as TGF-α levels in bronchoalveolar lavage fluid (BALF). Furthermore, the concentration of TGF-α in BALF was correlated with MUC5AC mRNA levels. Additionally, TGF-α expression was found to be positively correlated with MUC5AC expression in the airway epithelial cells of smokers. Compared with non-smoker asthma patients, TGF-α serum levels were also elevated in smoker asthma patients.

CONCLUSION

Autocrine TGF-α was associated with BaP-induced MUC5AC expression in vitro and in vivo. BaP induced TGF-α secretion by activating AhR and producing ROS, which led to activation of the EGFR-ERK pathway.

摘要

目的

苯并(a)芘(BaP)是一种环境污染物,在城市烟雾和香烟烟雾中浓度很高,据报道可促进高粘蛋白 5AC(MUC5AC)表达。上皮细胞来源的炎症细胞因子被认为是粘液过度分泌和 MUC5AC 过度表达的重要调节剂。在这里,我们研究了 BaP 对 MUC5AC 过度表达的影响是否与体内和体外的细胞因子自分泌活性有关。

方法

体内,用卵清蛋白(OVA)处理 BALB/c 小鼠,存在或不存在 BaP。通过阿尔辛蓝过碘酸希夫(AB-PAS)染色评估过敏诱导的粘液产生。体外使用人气道上皮细胞系 NCI-H292。实时定量 PCR 评估 MUC5AC 和转化生长因子(TGF)-α mRNA 水平。通过 ELISA 测量细胞因子的浓度。通过 Western 印迹检测细胞中 MUC5AC、p-ERK、ERK、p-EGFR 和 EGFR 蛋白,或通过免疫组化检测小鼠肺中的 MUC5AC、p-ERK、ERK、p-EGFR 和 EGFR 蛋白。使用小干扰 RNA 进行基因沉默。

结果

BaP 处理的 NCI-H292 细胞上清液中 TGF-α 过度产生。TGF-α 表达的敲低抑制了 BaP 诱导的 MUC5AC 表达增加以及随后的 EGFR-ERK 信号通路激活。敲低芳香烃受体(AhR)表达或用 ROS 抑制剂(N-乙酰-L-半胱氨酸)处理可减轻上皮细胞中 BaP 诱导的 TGF-α 分泌。在动物研究中,BaP 与 OVA 共暴露增加了肺中的粘液产生、MUC5AC 表达和 ROS-EGFR-ERK 激活以及支气管肺泡灌洗液(BALF)中的 TGF-α 水平。此外,BALF 中的 TGF-α 浓度与 MUC5AC mRNA 水平相关。此外,在吸烟者的气道上皮细胞中发现 TGF-α 表达与 MUC5AC 表达呈正相关。与非吸烟者哮喘患者相比,吸烟者哮喘患者的 TGF-α 血清水平也升高。

结论

自分泌 TGF-α与体外和体内 BaP 诱导的 MUC5AC 表达有关。BaP 通过激活 AhR 和产生 ROS 诱导 TGF-α 分泌,从而激活 EGFR-ERK 通路。

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