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Updated: Feb 18, 2026

Murine Model of Allergen Induced Asthma
Published on: May 14, 2012
[Lung injury in ovalbumin-challenged asthma mice induced by high-dose PM2.5 and its mechanism]
Abstract:
Objective To investigate the degree of lung injury induced by different doses of particulate matter with diameters ≤2.5 microm (PM2.5) in asthmatic mice. Methods Male BALB/c mice were randomly divided into normal control group, ovalbumin (OVA) asthma group, 1, 5, 15 mg/mL PM2.5 treated OVA asthma group. The bronchoalveolar lavage fluid (BALF) was collected and the number of white blood cells was observed by Gimsa staining. ELISA was used to determine the concentrations of serum cytokines interferon γ (IFN-γ), interleukin 17 (IL-17) and IL-10 in the peripheral blood of mice. Real-time quantitative PCR was performed to detect the mRNA expression levels of Toll-like receptor 4 (TLR4), nuclear factor-κB (NF-κB) in peripheral blood mononuclear cells (PBMCs). The levels of T-bet, RORγt and FOXP3 were tested by Western blotting. The lung tissues were collected and the pathological changes were observed by HE staining. Results Compared with the normal control group, the OVA asthma group showed thickened alveolar septum, enlarged alveolar cavity and more obvious inflammatory cell infiltration, as well as significantly increased white blood cells associated with inflammatory response in the BALF. Whereas, compared with the OVA asthma group, the above mentioned changes in 15 mg/mL PM2.5 treated OVA asthma group were extremely obvious. ELISA showed that the levels of IFN-γ and IL-10 in the serum of the OVA asthma group were significantly lower than those in the control group, while IL-17 significantly increased. Compared with the OVA asthma group, the levels of IFN-γ and IL-10 in 15 mg/mL PM2-treated OVA asthma group significantly decreased, while the content of IL-17 significantly increased. Real-time quantitative PCR showed that the expressions of TLR4 and NF-κB in PBMCs of the OVA asthma group were significantly higher than those in the control group. In 15 mg/mL PM2.5-treated OVA asthma group, the levels of TLR4 and NF-κB increased significantly as compared with the OVA asthma group. Compared with the control group, the expressions of T-bet and FOXP3 proteins in the OVA asthma group were significantly lower than those in the control group, and the expression of RORγt protein was significantly increased. Compared with the OVA asthma group, the levels of T-bet and FOXP3 proteins were reduced a lot in 15 mg/mL PM2.5-treated OVA asthma group, while RORγt protein level was remarkably elevated. Conclusion The 15 mg/mL PM2.5 can obviously promote OVA-induced asthma and even lung injury by activating the TLR4/NF-κB signaling pathway.
Insights
High concentrations of fine particulate matter (PM2.5) worsen ovalbumin-induced asthma in mice. PM2.5 exposure exacerbates lung injury and inflammation by activating the Toll-like receptor 4 (TLR4)/nuclear factor-κB (NF-κB) pathway.
Area of Science:
- Environmental Health
- Immunology
- Pulmonology
Background:
- Asthma is a chronic respiratory disease characterized by airway inflammation.
- Particulate matter with diameters ≤2.5 microm (PM2.5) is a common air pollutant linked to respiratory issues.
- The impact of PM2.5 on asthma severity and lung injury requires further investigation.
Purpose of the Study:
- To investigate the effects of different doses of PM2.5 on lung injury in a mouse model of asthma.
- To elucidate the underlying molecular mechanisms, including the Toll-like receptor 4 (TLR4)/nuclear factor-κB (NF-κB) signaling pathway.
Main Methods:
- Ovalbumin (OVA)-induced asthma model in BALB/c mice.
- Exposure to varying concentrations of PM2.5 (0, 1, 5, 15 mg/mL).
- Analysis of bronchoalveolar lavage fluid (BALF), serum cytokines (IFN-γ, IL-17, IL-10), gene expression (TLR4, NF-κB), protein levels (T-bet, RORγt, FOXP3), and lung tissue histology (HE staining).
Main Results:
- PM2.5 exposure, particularly at 15 mg/mL, significantly worsened OVA-induced asthma symptoms and lung injury.
- Increased inflammatory cell infiltration, elevated IL-17, and decreased IFN-γ and IL-10 levels were observed with higher PM2.5 doses.
- PM2.5 exposure upregulated TLR4, NF-κB, and RORγt, while downregulating T-bet and FOXP3 expression.
Conclusions:
- PM2.5 significantly promotes OVA-induced asthma and lung injury in mice.
- The TLR4/NF-κB signaling pathway is implicated in PM2.5-induced exacerbation of asthma.
- These findings highlight the detrimental role of PM2.5 in respiratory health, particularly for individuals with asthma.
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