BALB/c和C57BL/6小鼠局部变应性鼻炎模型免疫应答的初步研究

IF 2.5 3区 医学 Q1 OTORHINOLARYNGOLOGY
Qidi Zhang, Wanting Zhu, Zhixin Zou, Wenting Yu, Pei Gao, Ying Wang, Jianjun Chen
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引用次数: 3

摘要

背景:BALB/c和C57BL/6是过敏症研究中常用的小鼠品系。本研究在局部变应性鼻炎模型中研究了这两种小鼠株的免疫学差异。方法:18只BALB/c和18只C57BL/6小鼠鼻内注射不同剂量的卵清蛋白(OVA),连续8周(每株小鼠分为3个亚组,25 mg/mL组、0.25 mg/mL组和PBS组)。观察过敏症状、ova特异性血清抗体(IgE、IgG1、IgG2a)、脾培养上清细胞因子(IL-4、IFN-γ、IL-10)、局部鼻黏膜嗜酸性粒细胞浸润及杯状细胞的变化。应用RNA-seq技术检测局部鼻黏膜差异基因表达。结果:在相同剂量的OVA刺激下,C57BL/6组过敏症状加重比BALB/c组更明显。BALB/c血清IgE、IgG1、IgG2a逐渐升高,C57BL/6血清IgE、IgG1抗体减少,IgG2a抗体不升高。BALB/c脾细胞培养上清IL-4、IL-10随剂量增加而升高,IFN-γ在中剂量组显著升高,而IL-4、IL-10、IFN-γ在C57BL/6组无升高。两种小鼠嗜酸性粒细胞和杯状细胞的浸润与剂量成正比,C57BL/6高于BALB/c。RNA-seq结果显示,与BALB/c相比,C57BL/6的先天免疫应答、免疫系统过程功能、Jun kinase (JNK)通路和MAPKK通路上调。导致两种变应性鼻炎小鼠免疫反应差异的核心基因为Kng2、Kng1、Gnb3、Lpar3、Lpar1、Pik3r1、Pf4、Apob、Rps9和fbx2。结论:BALB/c小鼠与C57BL/6小鼠的免疫应答存在显著差异。BALB/c小鼠出现轻微的局部过敏性炎症反应和较强的全身免疫反应。相比之下,C57BL/6小鼠具有较强的局部过敏性炎症反应和相对较轻的全身免疫反应。可根据研究目的选择不同的小鼠品系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Preliminary Study in Immune Response of BALB/c and C57BL/6 Mice with a Locally Allergic Rhinitis Model.

Background: BALB/c and C57BL/6 mouse strains are commonly used in allergy research. The current study investigated the immunological differences between these two mouse strains with a locally allergic rhinitis model.

Methods: Eighteen BALB/c and eighteen C57BL/6 mice received different doses of ovalbumin (OVA) intranasally for eight weeks (each mouse strain has three subgroups, 25 mg/mL group, 0.25 mg/mL group, and the PBS group). The allergic symptoms, OVA-specific serum antibody (IgE, IgG1, IgG2a), cytokines (IL-4, IFN-γ, IL-10) in the splenic culture supernatant, infiltrating eosinophils and goblet cells in local nasal mucosa were measured. RNA-seq technology was applied to detect differential gene expression in the local nasal mucosa.

Results: With the same dose of OVA stimulation, the exacerbation of allergic symptoms was more pronounced in C57BL/6 than in BALB/c. BALB/c serum IgE, IgG1, and IgG2a gradually increased, and C57BL/6 produced fewer serum antibodies IgE and IgG1, while IgG2a never increased. BALB/c spleen cell culture supernatant IL-4 and IL-10 increased with increasing dose, and IFN-γ increased significantly in the intermediate dose group, while IL-4, IL-10, and IFN-γ did not increase in C57BL/6. The infiltration of eosinophils and goblet cells in both mice was proportional to the dose, while C57BL/6 was elevated more than BALB/c. RNA-seq suggested that the innate immune response, immune system process function, Jun kinase (JNK) pathway, and MAPKK pathway were upregulated in C57BL/6 compared to BALB/c. The core genes responsible for the differential immune response in both mice with allergic rhinitis were Kng2, Kng1, Gnb3, Lpar3, Lpar1, Pik3r1, Pf4, Apob, Rps9, and Fbxo2.

Conclusion: There are significant differences in the immunologic responses between BALB/c mice and C57BL/6 mice. BALB/c mice developed mild local allergic inflammatory reactions and strong systemic immune responses. In contrast, C57BL/6 mice had stronger local allergic inflammatory responses and relatively mild systemic immune responses. Different mice strains can be selected according to the research purpose.

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来源期刊
CiteScore
5.60
自引率
11.50%
发文量
82
审稿时长
4-8 weeks
期刊介绍: The American Journal of Rhinology & Allergy is a peer-reviewed, scientific publication committed to expanding knowledge and publishing the best clinical and basic research within the fields of Rhinology & Allergy. Its focus is to publish information which contributes to improved quality of care for patients with nasal and sinus disorders. Its primary readership consists of otolaryngologists, allergists, and plastic surgeons. Published material includes peer-reviewed original research, clinical trials, and review articles.
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