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miR-146a 表达降低可增强酒精和烧伤损伤后的肠道炎症。

Reduced Expression of miR-146a Potentiates Intestinal Inflammation following Alcohol and Burn Injury.

机构信息

Biochemistry, Molecular and Cancer Biology Program, Loyola University Chicago Health Sciences Division, Maywood, IL.

Burn and Shock Trauma Research Institute, Loyola University Chicago Health Sciences Division, Maywood, IL.

出版信息

J Immunol. 2024 Mar 1;212(5):881-893. doi: 10.4049/jimmunol.2300405.

DOI:10.4049/jimmunol.2300405
PMID:38189569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10922766/
Abstract

MicroRNAs (miRNAs) are small noncoding RNA molecules that negatively regulate gene expression. Within the intestinal epithelium, miRNAs play a critical role in gut homeostasis, and aberrant miRNA expression has been implicated in various disorders associated with intestinal inflammation and barrier disruption. In this study, we sought to profile changes in intestinal epithelial cell miRNA expression after alcohol and burn injury and elucidate their impact on inflammation and barrier integrity. Using a mouse model of acute ethanol intoxication and burn injury, we found that small intestinal epithelial cell expression of miR-146a is significantly decreased 1 d following injury. Using in vitro studies, we show that reduced miR-146a promotes intestinal epithelial cell inflammation by promoting p38 MAPK signaling via increased levels of its target TRAF6 (TNFR-associated factor 6). Furthermore, we demonstrate that in vivo miR-146a overexpression significantly inhibits intestinal inflammation 1 d following combined injury and potentially supports intestinal barrier homeostasis. Overall, this study highlights the important impact that miRNA expression can have on intestinal homeostasis and the valuable potential of harnessing aberrant miRNA expression as a therapeutic target to control intestinal inflammation.

摘要

微小 RNA(miRNAs)是一种小的非编码 RNA 分子,可负向调控基因表达。在肠上皮细胞中,miRNAs 在肠道稳态中发挥着关键作用,异常的 miRNA 表达与各种与肠道炎症和屏障破坏相关的疾病有关。在这项研究中,我们试图描绘酒精和烧伤损伤后肠上皮细胞 miRNA 表达的变化,并阐明它们对炎症和屏障完整性的影响。我们使用急性乙醇中毒和烧伤损伤的小鼠模型发现,损伤后 1 天,小肠上皮细胞中 miR-146a 的表达明显降低。通过体外研究,我们表明,降低的 miR-146a 通过增加其靶标 TRAF6(TNFR 相关因子 6)的水平促进 p38 MAPK 信号传导,从而促进肠道上皮细胞炎症。此外,我们证明,体内 miR-146a 过表达可显著抑制联合损伤后 1 天的肠道炎症,并可能支持肠道屏障稳态。总的来说,这项研究强调了 miRNA 表达对肠道稳态的重要影响,并突显了利用异常 miRNA 表达作为治疗靶点来控制肠道炎症的潜在价值。