Zhang Yueming, Li Qinyuan, Zhang Wen, Chen Weichao, Kong Zhenxuan, Zhang Guangli
Department of Respiratory Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children's Hospital of Chongqing Medical University, Chongqing, China; Department of Respiratory Medicine, Xi'an Children's Hospital, Xi'an, Shaanxi, China.
Department of Respiratory Medicine, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children's Hospital of Chongqing Medical University, Chongqing, China.
Int Immunopharmacol. 2025 Jul 16;163:115229. doi: 10.1016/j.intimp.2025.115229.
Ambient fine particulate matter (PM2.5) is believed to be closely connected to asthma severity. However, studies are needed to investigate the underlying mechanism of these findings. Our study attempted to confirm the role of NF-κB/NLRP3 pyroptosis in asthma exacerbation through in vivo and in vitro tests. We also analyzed the differentially expressed genes via RNA-Seq to investigate potential regulatory mechanisms.
We undertook in vivo and in vitro research to investigate the effects of PM2.5 on a mouse asthma model and the human bronchial epithelial cell line Beas-2b. Female BALB/c mice were sensitized with OVA to create a murine asthma model. HE staining and the EMAK system were used to assess airway inflammation and hyperresponsiveness in mouse lungs. We also measured IL-4, IL-5, IL-13, and OVA-specific IgE levels to assess the inflammatory effects of PM2.5 on both normal and OVA-induced asthmatic mice. Western blotting and immunohistochemistry were used to analyze the expression of major NF-κB and pyroptosis proteins. Human bronchial epithelial Beas-2b cells were treated with PM2.5, and the degree of pyroptosis was determined. RNA sequencing (RNA-Seq) was employed to identify differentially expressed genes and investigate potential regulatory mechanisms.
In vivo exposure to PM2.5 significantly increased HE staining scores in a mouse model of asthma. The levels of acetylcholine associated with enhanced airway responsiveness were lower in the PM2.5-exposed asthmatic group than in the control group. Compared with the asthmatic group, the BALF group presented considerably greater levels of IL-1β and IL-18. Compared with those in the asthmatic group, the protein expression levels of NLRP3, Caspase-1, GSDMD-N, cleaved Caspase-1p10, IL-1β, and p-NF-κBp65/NF-κBp65 in the lung tissues of the mice in the PM2.5 group were significantly greater than those in the asthmatic group. In vitro, PM2.5 causes pyroptosis and inflammation in Beas-2B human bronchial epithelial cells via the NF-κB/NLRP3 pathway. The TLR4 inhibitor TAK242 can partially block this effect.
In the OVA-induced asthma mouse model, PM2.5 activates the NF-κB/NLRP3 pathway and induces pyroptosis, thereby exacerbating airway inflammation and hyperreactivity. It may activate the NF-κB signalling cascade through the TLR4/MyD88 pathway, upregulate critical proteins in the pyroptosis pathway, and induce pyroptosis and inflammation in respiratory epithelial Beas-2b cells, exacerbating asthma.
环境细颗粒物(PM2.5)被认为与哮喘严重程度密切相关。然而,需要开展研究来探究这些发现的潜在机制。我们的研究试图通过体内和体外试验来证实核因子κB(NF-κB)/NLRP3炎性小体介导的细胞焦亡在哮喘加重中的作用。我们还通过RNA测序(RNA-Seq)分析差异表达基因,以探究潜在的调控机制。
我们进行了体内和体外研究,以探究PM2.5对小鼠哮喘模型和人支气管上皮细胞系Beas-2b的影响。用卵清蛋白(OVA)致敏雌性BALB/c小鼠以建立小鼠哮喘模型。采用苏木精-伊红(HE)染色和气道反应性监测系统评估小鼠肺部的气道炎症和高反应性。我们还检测了白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-13(IL-13)和OVA特异性免疫球蛋白E(IgE)水平,以评估PM2.5对正常小鼠和OVA诱导的哮喘小鼠的炎症作用。采用蛋白质免疫印迹法和免疫组织化学法分析主要NF-κB和细胞焦亡相关蛋白的表达。用PM2.5处理人支气管上皮Beas-2b细胞,并测定细胞焦亡程度。采用RNA测序(RNA-Seq)鉴定差异表达基因并探究潜在的调控机制。
在哮喘小鼠模型中,体内暴露于PM2.5显著增加了HE染色评分。与对照组相比,暴露于PM2.5的哮喘组中与气道反应性增强相关的乙酰胆碱水平较低。与哮喘组相比,支气管肺泡灌洗液(BALF)组中IL-1β和IL-18水平显著更高。与哮喘组相比,PM2.5组小鼠肺组织中NLRP3、半胱天冬酶-1(Caspase-1)、Gasdermin D-N端(GSDMD-N)、裂解的Caspase-1 p10、IL-1β以及磷酸化NF-κB p65/总NF-κB p65的蛋白表达水平显著高于哮喘组。在体外,PM2.5通过NF-κB/NLRP3途径诱导Beas-2B人支气管上皮细胞发生细胞焦亡和炎症反应。Toll样受体4(TLR4)抑制剂TAK242可部分阻断这种作用。
在OVA诱导的哮喘小鼠模型中,PM2.5激活NF-κB/NLRP3途径并诱导细胞焦亡,从而加剧气道炎症和高反应性。它可能通过TLR4/髓样分化因子88(MyD88)途径激活NF-κB信号级联反应,上调细胞焦亡途径中的关键蛋白,并诱导呼吸道上皮Beas-2b细胞发生细胞焦亡和炎症反应,从而加重哮喘。