Murine model of eosinophilic chronic rhinosinusitis with nasal polyposis inducing neuroinflammation and olfactory dysfunction

被引:2
|
作者
Huang, Wei-Hao [1 ]
Hung, Yu-Wen [2 ]
Hung, Wei [1 ,3 ]
Lan, Ming-Ying [1 ,3 ]
Yeh, Chien-Fu [1 ,3 ]
机构
[1] Taipei Vet Gen Hosp, Dept Otorhinolaryngol Head & Neck Surg, Sec 2,Shipai Rd, Taipei City 11217, Taiwan
[2] Yuanpei Univ Med Technol, Coll Med Technol & Nursing, Dept Nursing, Hsinchu, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Sch Med, Dept Otorhinolaryngol, Taipei, Taiwan
关键词
Eosinophilic chronic rhinosinusitis; nasal polyp; olfac- tory dysfunction; neuroinflammation; mouse model; olfactory sen- sory neuron; HOUSE-DUST-MITE; ASPERGILLUS PROTEASE; INFLAMMATION; REVEALS; MUCOSA;
D O I
10.1016/j.jaci.2024.02.021
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Chronic rhinosinusitis (CRS) is a common inflammatory condition affecting the nasal and paranasal sinus mucosa, often accompanied by olfactory dysfunction. Eosinophilic CRS with nasal polyps (ECRSwNP) is a subtype of CRS characterized by eosinophilic infiltration. Animal models for ECRSwNP with olfactory dysfunction are necessary for exploring potential therapeutic strategies. Objective: The aim of this study was to establish a mouse model of ECRSwNP combined with olfactory dysfunction in a shorter time frame using intranasal ovalbumin and Aspergillus protease (AP) administration. The efficacy of the model was validated by evaluating sinonasal inflammation, cytokine levels, olfactory function, and neuroinflammation in the olfactory bulb. Methods: Male BALB/c mice were intranasally administered ovalbumin and AP for 6 and 12 weeks to induce ECRSwNP. The resultant ECRSwNP mouse model underwent histologic assessment, cytokine analysis of nasal lavage fluid, olfactory behavioral tests, and gene expression profiling to identify neuroinflammatory markers within the olfactory bulb. Results: The developed mouse model exhibited substantial eosinophil infiltration, increased levels of inflammatory cytokines in nasal lavage fluid, and confirmed olfactory dysfunction through behavioral assays. Furthermore, olfactory bulb inflammation and reduced mature olfactory sensory neurons were observed in the model. Conclusion: This study successfully established a validated mouse model of ECRSwNP with olfactory dysfunction within a remarkably short span of 6 weeks, providing a valuable tool for condition. The model offers an efficient approach for future research in CRS with nasal polyps and olfactory dysfunction. (J Allergy Clin Immunol 2024;154:325-39.)
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页数:18
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