首页> 外文期刊>International journal of molecular medicine >Extracellular vesicles derived from human placental mesenchymal stem cells alleviate experimental colitis in?mice by inhibiting inflammation and oxidative stress
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Extracellular vesicles derived from human placental mesenchymal stem cells alleviate experimental colitis in?mice by inhibiting inflammation and oxidative stress

机译:通过抑制炎症和氧化应激来减轻人胎盘间充质干细胞的细胞外囊泡缓解实验性结肠炎。

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Mesenchymal stem cells (MSCs) are pluripotent cells that can be applied to the treatment of immune disorders, including inflammatory bowel disease (IBD). The therapeutic effects of MSCs have been mostly attributed to the secretion of soluble factors with paracrine actions, such as extracellular vesicles (EVs), which may play a relevant role in the repair of damaged tissues. In the present study, a mouse model of colitis was induced with the use of trinitrobenzene sulfonic acid (TNBS). EVs derived from human placental mesenchymal stem cells (hP?MSCs) were used for the treatment of colitis by in?situ injection. Clinical scores were applied to verify the therapeutic effects of EVs on mice with colitis. Inflammation in the colon was evaluated by measuring the levels of various inflammatory cytokines. The content of reactive oxygen species (ROS) was detected by the use of molecular imaging methods for real?time tracking and the therapeutic effects of EVs on mucosal healing in mice with colitis were evaluated. The results revealed that the injection of EVs regulated the balance of pro?inflammatory and anti?inflammatory cytokines in colon tissue. Treatment with EVs also suppressed oxidative stress by decreasing the activity of myeloperoxidase (MPO) and ROS. Histological analysis further confirmed that the EVs significantly promoted mucosal healing, as re?ected by the promotion of the proliferation of colonic epithelial cells and the maintenance of tight junctions. Taken together, the findings of the present study demonstrated that EVs derived from hP?MSCs alleviated TNBS?induced colitis by inhibiting inflammation and oxidative stress. These findings may provide a novel theoretical basis for the EV?based treatment of IBD.
机译:间充质干细胞(MSCs)是多能细胞,可用于治疗免疫疾病,包括炎症性肠病(IBD)。 MSCs的治疗效果主要归因于邻静脉作用的可溶因子的分泌,例如细胞外囊泡(EVS),其在受损组织的修复中可能发挥相关作用。在本研究中,使用三硝基苯磺酸(TNB)诱导结肠炎的小鼠模型。来自人胎盘间充质干细胞(HP?MSCs)衍生的EVS用于通过In in in an in an instue注射液。应用临床评分以验证EVS对结肠炎小鼠的治疗效果。通过测量各种炎性细胞因子的水平来评估结肠炎症。通过使用用于实际的分子成像方法检测反应性氧物质(ROS)的含量,评估了在结肠炎粘膜下对小鼠粘膜愈合的时间跟踪和EV的治疗效果。结果表明,EVS的注射调节了炎症性和抗炎症细胞因子在结肠组织中的平衡。通过降低髓过氧化物酶(MPO)和ROS的活性,EVS的处理也抑制了氧化应激。组织学分析进一步证实,EVS显着促进了粘膜愈合,如促进结肠上皮细胞增殖和紧密交叉点的维持。在一起,本研究的发现证明了来自HP的EVS衍生自HP?MSCs通过抑制炎症和氧化应激而诱导结肠炎。这些发现可以为EV的重要理论依据提供基于IBD的待遇。

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