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白细胞介素-13信号传导的基因变异与人类哮喘和特应性疾病

Genetic variants of IL-13 signalling and human asthma and atopy.

作者信息

Heinzmann A, Mao X Q, Akaiwa M, Kreomer R T, Gao P S, Ohshima K, Umeshita R, Abe Y, Braun S, Yamashita T, Roberts M H, Sugimoto R, Arima K, Arinobu Y, Yu B, Kruse S, Enomoto T, Dake Y, Kawai M, Shimazu S, Sasaki S, Adra C N, Kitaichi M, Inoue H, Yamauchi K, Tomichi N, Kurimoto F, Hamasaki N, Hopkin J M, Izuhara K, Shirakawa T, Deichmann K A

机构信息

University Children's Hospital, University of Freiburg, Freiburg, Germany.

出版信息

Hum Mol Genet. 2000 Mar 1;9(4):549-59. doi: 10.1093/hmg/9.4.549.

Abstract

Asthma and atopy show epidemiological association and are biologically linked by T-helper type 2 (T(h)2) cytokine-driven inflammatory mechanisms. IL-4 operates through the IL-4 receptor (IL-4R, a heterodimer of IL-4Ralpha and either gammac or IL-13Ralpha1) and IL-13 operates through IL-13R (a heterodimer of IL-4Ralpha and IL-13Ralpha1) to promote IgE synthesis and IgE-based mucosal inflammation which typify atopy. Recent animal model data suggest that IL-13 is a central cytokine in promoting asthma, through the stimulation of bronchial epithelial mucus secretion and smooth muscle hyper-reactivity. We investigated the role of common genetic variants of IL-13 and IL-13Ralpha1 in human asthma, considering IgE levels. A novel variant of human IL-13, Gln110Arg, on chromosome 5q31, associated with asthma rather than IgE levels in case-control populations from Britain and Japan [peak odds ratio (OR) = 2.31, 95% CI 1.33-4.00]; the variant also predicted asthma and higher serum IL-13 levels in a general, Japanese paediatric population. Immunohistochemistry demonstrated that both subunits of IL-13R are prominently expressed in bronchial epithelium and smooth muscle from asthmatic subjects. Detailed molecular modelling analyses indicate that residue 110 of IL-13, the site of the charge-modifying variants Arg and Gln, is important in the internal constitution of the ligand and crucial in ligand-receptor interaction. A non-coding variant of IL-13Ralpha1, A1398G, on chromosome Xq13, associated primarily with high IgE levels (OR = 3. 38 in males, 1.10 in females) rather than asthma. Thus, certain variants of IL-13 signalling are likely to be important promoters of human asthma; detailed functional analysis of their actions is needed.

摘要

哮喘与特应性在流行病学上存在关联,并且在生物学上通过2型辅助性T(Th2)细胞因子驱动的炎症机制相联系。白细胞介素-4(IL-4)通过IL-4受体(IL-4R,由IL-4Rα与γc或IL-13Rα1组成的异二聚体)发挥作用,而IL-13通过IL-13受体(由IL-4Rα与IL-13Rα1组成的异二聚体)发挥作用,以促进免疫球蛋白E(IgE)的合成以及以IgE为基础的黏膜炎症,后者是特应性的典型特征。最近的动物模型数据表明,IL-13通过刺激支气管上皮黏液分泌和平滑肌高反应性,在促进哮喘方面是一种核心细胞因子。我们研究了IL-13和IL-13Rα1的常见基因变异在人类哮喘中的作用,并考虑了IgE水平。位于5号染色体q31区域的人类IL-13的一种新变异体Gln110Arg,在英国和日本的病例对照人群中与哮喘相关,而不是与IgE水平相关[最高比值比(OR)=2.31,95%可信区间1.33 - 4.00];在一个日本普通儿科人群中,该变异体也预示着哮喘和更高的血清IL-13水平。免疫组织化学显示,IL-13R的两个亚基在哮喘患者的支气管上皮和平滑肌中均有显著表达。详细的分子建模分析表明,IL-13的第110位残基,即电荷修饰变异体精氨酸(Arg)和谷氨酰胺(Gln)所在的位点,在配体的内部结构中很重要,并且在配体-受体相互作用中起关键作用。位于X染色体q13区域的IL-13Rα1的一个非编码变异体A1398G,主要与高IgE水平相关(男性OR = 3.38,女性OR = 1.10),而不是与哮喘相关。因此,IL-13信号传导的某些变异体可能是人类哮喘的重要促进因素;需要对其作用进行详细的功能分析。

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