Department of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal Tumor, Nanfang Hospital, The First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong 510515, China.
Department of General Surgery, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, Jiangsu 210002, China.
Dis Markers. 2021 Sep 29;2021:7107705. doi: 10.1155/2021/7107705. eCollection 2021.
Overexpression of C-X-C motif chemokine receptor 4 (CXCR4) and intercellular cell adhesion molecule-1 (ICAM-1) may promote homing of mesenchymal stem cells (MSC). In this study, we treated ulcerative colitis animals with MSC preconditioned with or without H19 and compared the therapeutic effect of MSC and MSC-H19. We evaluated the regulatory relationship of H19 vs. miR-141/miR-139 and miR-141/miR-139 vs. ICAM-1/CXCR4. We established an ulcerative colitis mouse model to assess the effect of MSC and MSC-H19. H19 was found to bind to miR-141 and miR-139. The activity of H19 was strongly decreased in cells c-transfected with miR-141/miR-139 and WT H19. ICAM-1 was confirmed to be targeted by miR-141 and CXCR4 was targeted by miR-139. The H19 expression showed a negative regulatory relationship with the miR-141 and miR-139 expression but a positive regulatory relationship with the ICAM-1 and CXCR4 expression. In summary, the overexpression of H19 in MSC downregulated miR-139 and miR-141, thus increasing the activity of their targets ICAM-1 and CXCR4, respectively, to exhibit therapeutic effects in ulcerative colitis.
细胞间黏附分子-1(ICAM-1)和 C-X-C 基序趋化因子受体 4(CXCR4)的过表达可能促进间充质干细胞(MSC)归巢。在这项研究中,我们用预处理过或未预处理过 H19 的 MSC 治疗溃疡性结肠炎动物,并比较了 MSC 和 MSC-H19 的治疗效果。我们评估了 H19 与 miR-141/miR-139 以及 miR-141/miR-139 与 ICAM-1/CXCR4 的调节关系。我们建立了溃疡性结肠炎小鼠模型来评估 MSC 和 MSC-H19 的效果。发现 H19 与 miR-141 和 miR-139 结合。WT H19 与 miR-141/miR-139 共转染的细胞中 H19 的活性大大降低。证实 ICAM-1 是 miR-141 的靶标,而 CXCR4 是 miR-139 的靶标。H19 的表达与 miR-141 和 miR-139 的表达呈负相关,而与 ICAM-1 和 CXCR4 的表达呈正相关。总之,MSC 中 H19 的过表达下调了 miR-139 和 miR-141,从而分别增加了它们的靶标 ICAM-1 和 CXCR4 的活性,在溃疡性结肠炎中表现出治疗效果。