Hu Binbin, Wang Yan, Zheng Guotong, Zhang Hailin, Ni Liyan
The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
World Allergy Organ J. 2021 Oct 1;14(9):100582. doi: 10.1016/j.waojou.2021.100582. eCollection 2021 Sep.
We wanted to investigate whether parasympathetic inhibition affected the expression of type 2 innate lymphoid cells (ILC2s) in the nasal mucosa of a mouse model of allergic rhinitis (AR).
Thirty male C57BL/6 mice were randomly divided into 3 groups: control group, AR group, AR-treated group. AR nasal symptoms were assessed on a semi-quantitative scale according to the frequencies of nose rubbing and sneezing and the degree of rhinorrhea. The expression of cytokines protein in serum was detected by enzyme linked immunosorbent assay (ELISA). The number of ILC2s in nasal mucosa was detected by immunofluorescence double staining assay. Quantitative real-time Polymerase Chain Reaction (qPCR) was used to detect the expression of ILC2-associated factor in nasal mucosa.
The symptom scores of the AR group were significantly higher than those of the control group and AR-treated group. The expression levels of mouse ovalbumin (OVA) specific IgE, IL4, IL5, and IL13 in the serum of AR group were significantly higher than those in the control group and AR-treated group. The number of ILC2s and the gene expression of ILC2s related factors GATA3, CD25 and CD90 (Thy1) in the nasal mucosa of the AR group were significantly higher than those of the control group and AR-treated group.
We found that parasympathetic inhibition relieved AR symptoms and inhibited immune response of AR mice. ILC2s play an important role in the occurrence and development of AR, and parasympathetic nerve inhibition reduced the number of ILC2s and inhibited the cytokines expression by ILC2s. Our data provide information on the mechanism of action of parasympathetic inhibition in AR.
我们想要研究副交感神经抑制是否会影响变应性鼻炎(AR)小鼠模型鼻黏膜中2型固有淋巴细胞(ILC2s)的表达。
30只雄性C57BL/6小鼠被随机分为3组:对照组、AR组、AR治疗组。根据蹭鼻和打喷嚏的频率以及鼻漏程度,采用半定量量表评估AR鼻症状。采用酶联免疫吸附测定(ELISA)检测血清中细胞因子蛋白的表达。采用免疫荧光双染色法检测鼻黏膜中ILC2s的数量。采用定量实时聚合酶链反应(qPCR)检测鼻黏膜中ILC2相关因子的表达。
AR组的症状评分显著高于对照组和AR治疗组。AR组血清中小鼠卵清蛋白(OVA)特异性IgE、IL4、IL5和IL13的表达水平显著高于对照组和AR治疗组。AR组鼻黏膜中ILC2s的数量以及ILC2s相关因子GATA3、CD25和CD90(Thy1)的基因表达显著高于对照组和AR治疗组。
我们发现副交感神经抑制可缓解AR症状并抑制AR小鼠的免疫反应。ILC2s在AR的发生和发展中起重要作用,副交感神经抑制减少了ILC2s的数量并抑制了ILC2s的细胞因子表达。我们的数据提供了关于副交感神经抑制在AR中作用机制的信息。