Department of Critical Care Medicine, The First Affiliated Hospital of Sun Yat-sen University , Guangzhou, China.
Bioengineered. 2020 Dec;11(1):1334-1349. doi: 10.1080/21655979.2020.1851476.
Regulatory mechanisms of microRNAs (miRNAs) in the development of intestinal sepsis are unclear. This study investigated the role of rno-miR-146b-5p in sepsis-induced intestinal injury. A rat sepsis model was created using the cecal ligation and puncture method. The expression profiles of miRNA and mRNA in sepsis rats were examined using miRNA and mRNA sequencing; rno-miR-146b was selected for further investigation. The mimics and inhibitors of rno-miR-146b-5p were transfected into IEC-6 cells and then with or without lipopolysaccharide (LPS) treatment, and the expressions of Kruppel-like factor 4 (Klf4) and Cyclin D2 (Ccnd2) were assessed by quantitative real-time transcriptase-polymerase chain reaction (qRT-PCR) and western blotting. Next, cell counting kit-8 assay was used to detect cell viability, and scratch wound healing assay was used to assess cell migration. In sepsis rat model, crypt cell proliferation was inhibited and crypt cell apoptosis was increased. Compared with the sham control, results of miRNA and mRNA sequencing showed that there were 17 miRNAs and 1617 mRNAs that were upregulated and 123 miRNAs and 1917 mRNAs that were downregulated in the sepsis model group. The network diagrams and qRT-PCR validation indicated that rno-miR-146b-5p may inhibit the expression of Klf4. By adjusting the expression of rno-miR-146b-5p in IEC-6 cells with or without LPS treatment, we found that increased expression of rno-miR-146b-5p inhibited cell proliferation and migration and inhibited the expression of Ccnd2. rno-miR-146b-5p may play a vital role in the development of sepsis intestinal injury through targeting Klf4 expression and affecting promoter activity of Ccnd2.
miRNAs(miRNA)在肠败血症发展中的调控机制尚不清楚。本研究探讨了 rno-miR-146b-5p 在脓毒症诱导的肠损伤中的作用。采用盲肠结扎穿孔法建立大鼠脓毒症模型。采用 miRNA 和 mRNA 测序检测脓毒症大鼠中 miRNA 和 mRNA 的表达谱;选择 rno-miR-146b 进行进一步研究。将 rno-miR-146b-5p 的模拟物和抑制剂转染至 IEC-6 细胞,然后用或不用脂多糖(LPS)处理,并通过定量实时转录酶聚合酶链反应(qRT-PCR)和蛋白质印迹法评估 Kruppel 样因子 4(Klf4)和细胞周期蛋白 D2(Ccnd2)的表达。接下来,使用细胞计数试剂盒-8 检测细胞活力,划痕愈合实验评估细胞迁移。在脓毒症大鼠模型中,隐窝细胞增殖受到抑制,隐窝细胞凋亡增加。与假手术对照组相比,miRNA 和 mRNA 测序结果显示,在脓毒症模型组中有 17 个 miRNA 和 1617 个 mRNA 上调,123 个 miRNA 和 1917 个 mRNA 下调。网络图和 qRT-PCR 验证表明,rno-miR-146b-5p 可能抑制 Klf4 的表达。通过调节 LPS 处理前后 IEC-6 细胞中 rno-miR-146b-5p 的表达,我们发现 rno-miR-146b-5p 表达增加抑制细胞增殖和迁移,并抑制 Ccnd2 的表达。rno-miR-146b-5p 可能通过靶向 Klf4 表达并影响 Ccnd2 启动子活性在脓毒症肠损伤的发展中发挥重要作用。