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哮喘患者支气管黏膜的全基因组甲基化分析:与特应性的关系。

Genome-wide methylation profiling of the bronchial mucosa of asthmatics: relationship to atopy.

机构信息

Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, 1174, Jung Dong, Wonmi-Gu, Bucheon, Gyeonggi Do 420-021, Korea.

出版信息

BMC Med Genet. 2013 Mar 24;14:39. doi: 10.1186/1471-2350-14-39.

Abstract

BACKGROUND

Asthma is a common respiratory disease that is characterized by bronchial hyperresponsiveness and airway obstruction due to chronic airway inflammation. Atopic asthma is a typical IgE-mediated disease in which the enhanced production of IgE is driven by the activation of Th2 cells, which release a distinct pattern of cytokines, including interleukin 4 (IL4) and IL3, in response to specific antigen presentation. To evaluate the methylation status of the whole genomes of bronchial mucosa tissues from subjects who lacked or had sensitization to Dermatophagoides farina (Df) and Dermatophagoides pteronyssinus (Dp).

METHODS

The genome-wide DNA methylation levels in the bronchial mucosa tissues of atopic asthmatics (N=10), non-atopic asthmatics (N=7), and normal controls (N=7) were examined using microarrays.

RESULTS

In the bronchial mucosa of atopic asthmatics, hypermethylation was detected at 6 loci in 6 genes, while hypomethylation was detected at 49 loci in 48 genes compared to those of non-atopic asthmatics. Genes that were assigned the ontologies of multicellular organismal process, response to organic substance, hormone metabolic process, and growth factor receptor binding were hypomethylated. The methylation levels in the mucosa of asthmatics and normal controls were similar.

CONCLUSIONS

The bronchial mucosa of asthmatics who are atopic to Df or Dp have characteristic methylation patterns for 52 genes. The genes and pathways identified in the present study may be associated with the presence of atopy in asthmatics and therefore represent attractive targets for future research.

摘要

背景

哮喘是一种常见的呼吸道疾病,其特征是由于慢性气道炎症导致支气管高反应性和气道阻塞。特应性哮喘是一种典型的 IgE 介导的疾病,其中 IgE 的增强产生是由 Th2 细胞的激活驱动的,Th2 细胞在对特定抗原呈递的反应中释放出独特的细胞因子模式,包括白细胞介素 4(IL4)和白细胞介素 3(IL3)。为了评估对屋尘螨(Df)和粉尘螨(Dp)无致敏或致敏的受试者支气管黏膜组织的全基因组甲基化状态。

方法

使用微阵列检测特应性哮喘患者(N=10)、非特应性哮喘患者(N=7)和正常对照者(N=7)的支气管黏膜组织的全基因组 DNA 甲基化水平。

结果

与非特应性哮喘患者相比,特应性哮喘患者的支气管黏膜中,有 6 个基因的 6 个位点检测到超甲基化,48 个基因的 49 个位点检测到低甲基化。被分配到多细胞生物过程、对有机物质的反应、激素代谢过程和生长因子受体结合等本体论的基因被低甲基化。哮喘患者和正常对照者的黏膜甲基化水平相似。

结论

对 Df 或 Dp 特应性的哮喘患者的支气管黏膜具有 52 个基因的特征性甲基化模式。本研究中鉴定的基因和途径可能与哮喘患者特应性的存在有关,因此代表了未来研究的有吸引力的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d744/3616917/f6825586461d/1471-2350-14-39-1.jpg

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