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在过敏性气道炎症中鉴定白细胞介素13诱导的表观遗传特征。

Identification of an interleukin 13-induced epigenetic signature in allergic airway inflammation.

作者信息

Ooi Aik T, Ram Sonal, Kuo Alan, Gilbert Jennifer L, Yan Weihong, Pellegrini Matteo, Nickerson Derek W, Chatila Talal A, Gomperts Brigitte N

出版信息

Am J Transl Res. 2012;4(2):219-28. Epub 2012 Apr 10.

Abstract

Epigenetic changes have been implicated in the pathogenesis of asthma. We sought to determine if IL13, a key cytokine in airway inflammation and remodeling, induced epigenetic DNA methylation and miRNAs expression changes in the airways in conjunction with its transcriptional gene regulation. Inducible expression of an IL13 transgene in the airways resulted in significant changes in DNA methylation in 177 genes, most of which were associated with the IL13 transcriptional signature in the airways. A large number of genes whose expression was induced by IL13 were found to have decreased methylation, including those involved in tissue remodeling (Olr1), leukocyte influx (Cxcl3, Cxcl5, CSFr2b), and the Th2 response (C3ar1, Chi3l4). Reciprocally, some genes whose expression was suppressed were found to have increased methylation (e.g. Itga8). In addition, miRNAs were identified with targets for lung development and Wnt signaling, amongst others. These results indicate that IL13 confers an epigenetic methylation and miRNA signature that accompanies its transcriptional program in the airways, which may play a critical role in airway inflammation and remodeling.

摘要

表观遗传变化与哮喘的发病机制有关。我们试图确定白细胞介素13(IL13),一种气道炎症和重塑中的关键细胞因子,在其转录基因调控的同时是否会诱导气道中表观遗传DNA甲基化和微小RNA(miRNA)表达的变化。气道中IL13转基因的可诱导表达导致177个基因的DNA甲基化发生显著变化,其中大多数与气道中的IL13转录特征相关。发现大量由IL13诱导表达的基因甲基化降低,包括那些参与组织重塑(Olr1)、白细胞流入(Cxcl3、Cxcl5、CSFr2b)和Th2反应(C3ar1、Chi3l4)的基因。相反,发现一些表达受抑制的基因甲基化增加(例如Itga8)。此外,还鉴定出了一些以肺发育和Wnt信号等为靶点的miRNA。这些结果表明,IL13赋予了一种表观遗传甲基化和miRNA特征,伴随其在气道中的转录程序,这可能在气道炎症和重塑中起关键作用。

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