Li Gehui, Xu Min, Wang Hao, Qi Xiaofei, Wang Xiaoguang, Li Yong, Sun Jing, Li Yuantao
Department of Anesthesiology, Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, Guangdong 518028, P.R. China.
Department of Anesthesiology, Xiangyang No.1 People's Hospital, Hubei University of Medicine, Xiangyang, Hubei 441000, P.R. China.
Exp Ther Med. 2021 Sep;22(3):937. doi: 10.3892/etm.2021.10369. Epub 2021 Jul 1.
Previous studies have shown that microRNAs (miRs), such as miR-146a play an important role in the pathogenesis of intestinal ischemia/reperfusion (I/R)-induced injury; however, the role of miR-146a in intestinal I/R-induced acute lung injury has not been elucidated. An intestinal I/R-induced injury mouse model was established in the present study by clamping the superior mesenteric artery and expression levels of miR-146a in intestinal and lung tissue samples were evaluated using reverse transcription-quantitative PCR (RT-qPCR). Intestinal and lung histopathological characteristics in mice with intestinal I/R-induced injury were assessed by hematoxylin and eosin staining, and mRNA and protein expression levels in intestinal and lung tissue samples were evaluated using RT-qPCR and western blotting, respectively. miR-146a expression was significantly downregulated in the intestinal and lung tissue samples of mice with intestinal I/R-induced injury. Intestinal I/R injury-induced histopathological changes in the lung and intestines, and pulmonary edema in mice transduced with an adenoviral miR-146a-overexpression vector (the miR-146a overexpression group) were alleviated. mRNA expression levels of TNF-α, IL-1β, IFN-γ and TGF-β1, and protein expression levels of TNF receptor-associated factor 6, phosphorylated-p65 NF-κB, cleaved caspase-3 and cleaved caspase-9 in lung and intestinal tissue samples were downregulated in I/R-miR-146a-overexpressing mice, compared with those from the I/R-negative control group. Thus, the present study identified that pre-treatment with the miR-146a overexpression vector alleviated intestinal I/R-induced acute lung injury in mice.
先前的研究表明,微小RNA(miR),如miR-146a,在肠道缺血/再灌注(I/R)诱导的损伤发病机制中发挥重要作用;然而,miR-146a在肠道I/R诱导的急性肺损伤中的作用尚未阐明。在本研究中,通过夹闭肠系膜上动脉建立了肠道I/R诱导损伤的小鼠模型,并使用逆转录定量PCR(RT-qPCR)评估肠道和肺组织样本中miR-146a的表达水平。通过苏木精和伊红染色评估肠道I/R诱导损伤小鼠的肠道和肺组织病理学特征,并分别使用RT-qPCR和蛋白质印迹法评估肠道和肺组织样本中的mRNA和蛋白质表达水平。在肠道I/R诱导损伤的小鼠的肠道和肺组织样本中,miR-146a表达明显下调。用腺病毒miR-146a过表达载体转导的小鼠(miR-146a过表达组)中,肠道I/R损伤诱导的肺和肠道组织病理学变化以及肺水肿得到缓解。与I/R阴性对照组相比,I/R-miR-146a过表达小鼠的肺和肠道组织样本中TNF-α、IL-1β、IFN-γ和TGF-β1的mRNA表达水平以及TNF受体相关因子6、磷酸化-p65 NF-κB、裂解的caspase-3和裂解的caspase-9的蛋白质表达水平均下调。因此,本研究确定用miR-146a过表达载体预处理可减轻小鼠肠道I/R诱导的急性肺损伤。