Alcohol Research Program, Burn and Shock Trauma Research Institute, Department of Surgery, Loyola University Chicago Health Sciences Campus, Maywood, IL 60153, USA.; Integrative Cell Biology Program, Loyola University Chicago Health Sciences Campus, Maywood, IL 60153, USA.
Alcohol Research Program, Burn and Shock Trauma Research Institute, Department of Surgery, Loyola University Chicago Health Sciences Campus, Maywood, IL 60153, USA..
Biochim Biophys Acta Mol Basis Dis. 2017 Oct;1863(10 Pt B):2645-2653. doi: 10.1016/j.bbadis.2017.03.025. Epub 2017 Apr 9.
Ethanol exposure at the time of burn injury is a major contributor to post-burn pathogenesis. Many of the adverse effects associated with ethanol and burn injury are linked to an impaired intestinal barrier. The combined insult causes intestinal inflammation, resulting in tissue damage, altered tight junction expression, and increased intestinal permeability. MicroRNAs play a critical role in maintaining intestinal homeostasis including intestinal inflammation and barrier function. Specifically, miR-150 regulates inflammatory mediators which can contribute to gut barrier disruption. The present study examined whether ethanol and burn injury alter expression of microRNA processing enzymes (Drosha, Dicer, and Argonaute-2) and miR-150 in the small intestine. Male mice were gavaged with ethanol (~2.9g/kg) 4h prior to receiving a ~12.5% total body surface area full thickness burn. One or three days after injury, mice were euthanized and small intestinal epithelial cells (IECs) were isolated and analyzed for expression of microRNA biogenesis components and miR-150. Dicer mRNA and protein levels were not changed following the combined insult. Drosha and Argonaute-2 mRNA and protein levels were significantly reduced in IECs one day after injury; which accompanied reduced miR-150 expression. To further determine the role of miR-150 in intestinal inflammation, young adult mouse colonocytes were transfected with a miR-150 plasmid and stimulated with LPS (100ng/ml). miR-150 overexpression significantly reduced IL-6 and KC protein levels compared to vector control cells challenged with LPS. These results suggest that altered microRNA biogenesis and associated decrease in miR-150 likely contribute to increased intestinal inflammation following ethanol and burn injury.
乙醇暴露是烧伤后发病机制的主要原因之一。许多与乙醇和烧伤相关的不良反应都与受损的肠道屏障有关。联合损伤导致肠道炎症,导致组织损伤、紧密连接表达改变和肠道通透性增加。microRNA 在维持肠道内稳态中起着关键作用,包括肠道炎症和屏障功能。具体来说,miR-150 调节炎症介质,可能导致肠道屏障破坏。本研究探讨了乙醇和烧伤是否改变了小肠中 microRNA 加工酶(Drosha、Dicer 和 Argonaute-2)和 miR-150 的表达。雄性小鼠在接受约 12.5%全身体表面积全层烧伤前 4 小时给予乙醇(~2.9g/kg)灌胃。损伤后 1 或 3 天,处死小鼠并分离小肠上皮细胞(IECs),分析 microRNA 生物发生成分和 miR-150 的表达。联合损伤后 Dicer mRNA 和蛋白水平没有变化。损伤后 1 天,Drosha 和 Argonaute-2 mRNA 和蛋白水平显著降低,同时 miR-150 表达降低。为了进一步确定 miR-150 在肠道炎症中的作用,用 miR-150 质粒转染成年小鼠结肠细胞,并用 LPS(100ng/ml)刺激。与用 LPS 刺激的载体对照细胞相比,miR-150 过表达显著降低了 IL-6 和 KC 蛋白水平。这些结果表明,microRNA 生物发生的改变和相关的 miR-150 减少可能导致乙醇和烧伤后肠道炎症增加。