The role of estrogen receptors and house dust mite-induced DNA methylation in a mouse model.

IF 3.8 2区 医学 Q1 PHYSIOLOGY
Sarah Commodore, Carolyn Damilola Ekpruke, Rachel Alford, Omar A Borges-Sosa, Dustin Rousselle, Maksat Babayev, Chukwudike Igwe, Christopher M Hemmerich, Douglas B Rusch, Patricia Silveyra
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Abstract

Asthma is a chronic respiratory disease affecting over 230 million people worldwide, with higher prevalence in women. Environmental allergens such as house dust mite (HDM) trigger airway inflammation and hyperresponsiveness (AHR), yet the epigenetic mechanisms underlying these responses remain poorly understood. Furthermore, the role of estrogen receptors in the context of asthma is understudied. We aimed to investigate whether estrogen receptor-specific DNA methylation contributes to HDM-induced airway remodeling and hyperresponsiveness. Male and female C57BL/6J wild-type mice and estrogen receptor α and β knockout mice (Esr1-/- and Esr2-/-) were exposed to HDM or phosphate-buffered saline for 5 wk. DNA methylation and RNA sequencing data were obtained from snap-frozen whole lung tissues. HDM exposure resulted in widespread differential methylation of genes associated with inflammation and AHR, including Itgal, Tmem267, Rap1b, Bmf, Mid1, Fgd1, Ddx4, Comtd1, Filip1l, Grb10, and Chst7. Notably, the absence of estrogen receptor β (in Esr2-/- mice) produced the most pronounced methylation patterns, particularly in females. Pathway enrichment analysis revealed asthma-relevant processes such as extracellular matrix remodeling, leukocyte adhesion and migration, airway smooth muscle contraction, and inflammatory signaling. Integration of methylation and gene expression data confirmed significant correlations (P < 0.05) for Itgal, Rap1b, and Tmem267, and a marginal correlation for Chst7 (P < 0.1), implicating these genes in allergic asthma pathogenesis. Our findings demonstrate that HDM exposure induces sex-specific epigenetic changes mediated by estrogen receptor status, highlighting a potential mechanism for increased asthma susceptibility in women. These results can inform estrogen receptor-targeted treatment strategies for allergic airway diseases.NEW & NOTEWORTHY Understanding estrogen receptor-mediated epigenetic regulation provides a foundation for developing sex-specific interventions for asthma, addressing the higher prevalence and severity observed in women. In this study, we demonstrate that exposure to house dust mite in the mouse lung is associated with epigenetic alterations in genes linked to airway hyperresponsiveness and lung inflammation. These alterations were dependent on the presence or absence of estrogen receptors.

雌激素受体和屋尘螨诱导的DNA甲基化在小鼠模型中的作用。
哮喘是一种慢性呼吸系统疾病,影响全球2.3亿多人,女性患病率更高。环境过敏原如屋尘螨(HDM)引发气道炎症和高反应性(AHR),然而这些反应背后的表观遗传机制仍然知之甚少。此外,雌激素受体在哮喘中的作用尚未得到充分研究。我们的目的是研究雌激素受体特异性DNA甲基化是否有助于hdm诱导的气道重塑和高反应性。将雄性和雌性C57BL/6J野生型小鼠和雌激素受体α和β敲除小鼠(Esr1-/-和Esr2-/-)暴露于HDM或磷酸盐缓冲盐水中5周。从快速冷冻的全肺组织中获得DNA甲基化和RNA测序数据。HDM暴露导致与炎症和AHR相关的基因广泛的差异甲基化,包括Itgal、Tmem267、Rap1b、Bmf、Mid1、Fgd1、Ddx4、comt1、filip11、Grb10和Chst7。值得注意的是,雌激素受体β的缺失(在Esr2-/-小鼠中)产生了最明显的甲基化模式,尤其是在雌性小鼠中。通路富集分析揭示了哮喘相关的过程,如细胞外基质重塑、白细胞粘附和迁移、气道平滑肌收缩和炎症信号。整合甲基化和基因表达数据证实了显著的相关性(pItgal, Rap1b和Tmem267)和Chst7的边际相关性(p
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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