Defence Institute of Physiology and Allied Sciences, Delhi, India.
Department of Botany, University of Delhi, Delhi, India.
Thromb Res. 2022 Jul;215:5-13. doi: 10.1016/j.thromres.2022.04.018. Epub 2022 May 2.
DNA methylation regulates gene expression by inhibiting transcription factor binding to promoter and regulatory regions. Acute hypoxia during altitude exposure is associated with decreased natural anticoagulants and morbid thrombotic events. Thrombomodulin (TM) is a high affinity thrombin binding receptor protein, vital for vascular homeostasis. The purpose of this study is to determine gene expression regulation via methylation of TM gene in high altitude hypoxia induced deep vein thrombosis (DVT) patients.
Percent 5-methyl cytosine analysis showed increased methylation in high altitude DVT patients (HAP) as compared to high altitude control (HAC) and seal level control (Control) subjects, while TM protein and mRNA levels were decreased in high altitude DVT patients as compared to other two groups. Bisulfite sequencing analysis indicated increased methylation in TM promoter in high altitude DVT patients compared to high altitude controls. Flow cytometry analysis showed decreased TM expression in hypoxia induced primary human umbilical vein endothelial cells (HUVECs). Treatment with specific DNA methyltransferase (DNMT) inhibitor-decitabine during hypoxia, restored TM expression. in vitro global methylation assay showed increased methylation in hypoxia group. Specific concentration of decitabine in hypoxia decreased global methylation showing a direct correlation between DNMTs and methylation. Selective dose of decitabine restored TM levels in HUVECs. DNMT1 and DNMT3B proteins showed to mediate the overall expression of TM.
TM emerged as a potential candidate for methylation in high altitude DVT patients, regulated by hypoxia-induced epigenetic mechanism. Hypoxia culminates in methylation of DNA sequences in the promoter region of TM gene and increased the expression of DNMT1 and DNMT3B per se in primary HUVECs. Critical DNA methylation events were found to be compromised in high altitude DVT patients.
DNA 甲基化通过抑制转录因子与启动子和调节区域的结合来调节基因表达。在海拔高度暴露期间的急性缺氧与天然抗凝剂减少和病态血栓形成事件有关。血栓调节蛋白(TM)是一种高亲和力的凝血酶结合受体蛋白,对血管稳态至关重要。本研究的目的是确定通过 TM 基因在高原缺氧诱导的深静脉血栓形成(DVT)患者中的甲基化来调节基因表达。
5-甲基胞嘧啶分析显示,与高原对照组(HAC)和海豹水平对照组(Control)相比,高原 DVT 患者(HAP)的甲基化增加,而与其他两组相比,高原 DVT 患者的 TM 蛋白和 mRNA 水平降低。亚硫酸氢盐测序分析表明,与高原对照组相比,高原 DVT 患者的 TM 启动子中甲基化增加。流式细胞术分析显示,缺氧诱导的原代人脐静脉内皮细胞(HUVEC)中 TM 表达降低。在缺氧期间用特异性 DNA 甲基转移酶(DNMT)抑制剂地西他滨治疗,恢复了 TM 表达。体外全甲基化测定显示缺氧组中甲基化增加。在缺氧组中,地西他滨的特定浓度降低了全甲基化,表明 DNMTs 与甲基化之间存在直接相关性。在 HUVECs 中,地西他滨的选择性剂量恢复了 TM 水平。DNMT1 和 DNMT3B 蛋白被证明介导 TM 的整体表达。
TM 成为高原 DVT 患者甲基化的潜在候选物,受缺氧诱导的表观遗传机制调节。缺氧导致 TM 基因启动子区域的 DNA 序列甲基化,并增加了原发性 HUVEC 中 DNMT1 和 DNMT3B 本身的表达。在高原 DVT 患者中发现关键的 DNA 甲基化事件受到损害。