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Tie2通路及基因在哮喘和变应性结膜炎中可能作用的研究

Investigation of the Possible Role of Tie2 Pathway and Gene in Asthma and Allergic Conjunctivitis.

作者信息

Gál Zsófia, Gézsi András, Molnár Viktor, Nagy Adrienne, Kiss András, Sultész Monika, Csoma Zsuzsanna, Tamási Lilla, Gálffy Gabriella, Bálint Bálint L, Póliska Szilárd, Szalai Csaba

机构信息

Department of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.

Institute of Genomic Medicine and Rare Disorders, Semmelweis University, Budapest, Hungary.

出版信息

Front Genet. 2020 Feb 27;11:128. doi: 10.3389/fgene.2020.00128. eCollection 2020.

Abstract

Tie2, coded by the gene, is a tyrosine kinase receptor and plays a central role in vascular stability. It was suggested that variations in the gene might influence the susceptibility to asthma and allergic conjunctivitis. The aim of this study was to further investigate these suggestions, involving different populations and to study the Tie2 related pathway on a mouse model of asthma. The discovery, stage I cohort involved 306 patients with moderate and severe allergic rhinitis, the stage II study consisted of four cohorts, namely, adult and pediatric asthmatics and corresponding controls. Altogether, there were 1,258 unrelated individuals in these cohorts, out of which 63.9% were children and 36.1% were adults. In stage I, 112 SNPs were screened in the gene of the patients in order to search for associations with asthma and allergic conjunctivitis. The top associated SNPs were selected for association studies on the replication cohorts. The rs3824410 SNP was nominally associated with a reduced risk of asthma in the stage I cohort and with severe asthma within the asthmatic population (p=0.009; OR=0.48) in the replication cohort. In the stage I study, 5 SNPs were selected in conjunctivitis. Due to the low number of adult patients with conjunctivitis, only children were involved in stage II. Within the asthmatic children, the rs622232 SNP was associated with conjunctivitis in boys in the dominant model (p=0.004; OR=4.76), while the rs7034505 showed association to conjunctivitis in girls (p=0.012; OR=2.42). In the lung of a mouse model of asthma, expression changes of 10 Tie2 pathway-related genes were evaluated at three points in time. Eighty percent of the selected genes showed significant changes in their expressions at least at one time point during the process, leading from sensitization to allergic airway inflammation. The expressions of both the gene and its ligands showed a reduced level at all time points. In conclusion, our results provide additional proof that the Tie2 pathway, the gene and its variations might have a role in asthma and allergic conjunctivitis. The gene and its associated pathways can be potential therapeutic targets in both diseases.

摘要

Tie2由该基因编码,是一种酪氨酸激酶受体,在血管稳定性中起核心作用。有人提出该基因的变异可能会影响哮喘和过敏性结膜炎的易感性。本研究的目的是进一步调查这些观点,涉及不同人群,并在哮喘小鼠模型上研究与Tie2相关的通路。发现阶段,I期队列包括306例中重度过敏性鼻炎患者,II期研究由四个队列组成,即成人和儿童哮喘患者及相应对照组。这些队列中共有1258名无亲属关系的个体,其中63.9%为儿童,36.1%为成人。在I期,在患者的该基因中筛选了112个单核苷酸多态性(SNP),以寻找与哮喘和过敏性结膜炎的关联。选择最相关的SNP用于在复制队列上进行关联研究。rs3824410 SNP在I期队列中与哮喘风险降低名义上相关,在复制队列的哮喘人群中与重度哮喘相关(p = 0.009;OR = 0.48)。在I期研究中,在结膜炎中选择了5个SNP。由于成人结膜炎患者数量较少,II期仅纳入儿童。在哮喘儿童中,rs622232 SNP在显性模型中与男孩的结膜炎相关(p = 0.004;OR = 4.76),而rs7034505与女孩的结膜炎相关(p = 0.012;OR = 2.42)。在哮喘小鼠模型的肺中,在三个时间点评估了10个与Tie2通路相关基因的表达变化。在从致敏到过敏性气道炎症的过程中,80%的选定基因至少在一个时间点显示出表达的显著变化。该基因及其配体的表达在所有时间点均显示出降低水平。总之,我们的结果提供了额外的证据,表明Tie2通路、该基因及其变异可能在哮喘和过敏性结膜炎中起作用。该基因及其相关通路可能是这两种疾病的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b597/7057532/2436f126f678/fgene-11-00128-g001.jpg

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