首页> 外文期刊>European Journal of Inflammation >Protective Effects of Mesenchymal Stem Cells with Transient Overexpression of Hmgb1 on Balloon-Induced Carotid Artery Injury:
【24h】

Protective Effects of Mesenchymal Stem Cells with Transient Overexpression of Hmgb1 on Balloon-Induced Carotid Artery Injury:

机译:Hmgb1短暂过表达的间充质干细胞对球囊诱发的颈动脉损伤的保护作用:

获取原文
       

摘要

Mesenchymal stem cells (MSC) play a crucial role in endothelial repair after artery injury. The high mobility group box 1 (HMGB1) is a key modulator of the homing of MSC to impaired artery and endothelialization. This study was aimed to determine whether balloon-induced carotid artery injury could be improved by transplantation with MSC modified by HMGB1. MSC were infected by adenoviral serotype 5 encoding recombinant green fluorescent protein (GFP) gene and HMGB1 (ad5GFP-HMGB1). The expression of HMGB1, vascular endothelial growth factor (VEGF) and proliferating cell nuclear antigen (PCNA) was detected in MSC using Real-time PCR, Western blot and semi-quantitative immunohistochemical assays. In vivo, reendothelialization was examined in rats subjected to carotid artery injury. The homing of MSC was observed under fluorescence microscopy, and the levels of serum tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP) was assessed by ELISA assay. As a result, compared with the MSC group, the expression of HMGB1, VEGF and PCNA was markedly increased, vascular reendothelialization was accelerated, and the levels of serum TNF-α and CRP were decreased in group ad5GFP and ad5GFP-HMGB1. Transplantation of MSC infected with adGFP-HMGB1 strengthened the MSC effect. Taken together, modification of HMGB1 can enhance the protective effects of MSC on balloon-induced carotid artery injury through up-regulation of VEGF and PCNA expression and inhibition of the inflammatory response. HMGB1 in MSC may represent a novel therapeutic target for the treatment of endothelial repair.
机译:间充质干细胞(MSC)在动脉损伤后的内皮修复中起着至关重要的作用。高迁移率族盒1(HMGB1)是MSC归巢到受损动脉和内皮化的关键调节剂。这项研究旨在确定通过HMGB1修饰的MSC移植能否改善球囊诱发的颈动脉损伤。 MSC被编码重组绿色荧光蛋白(GFP)基因和HMGB1(ad5GFP-HMGB1)的腺病毒血清型5感染。使用实时荧光定量PCR,Western印迹和半定量免疫组化方法检测MSC中HMGB1,血管内皮生长因子(VEGF)和增殖细胞核抗原(PCNA)的表达。在体内,在遭受颈动脉损伤的大鼠中检查了内皮再内皮化。在荧光显微镜下观察MSC的归巢,并通过ELISA法测定血清肿瘤坏死因子-α(TNF-α)和C反应蛋白(CRP)的水平。结果,与MSC组相比,ad5GFP和ad5GFP-HMGB1组中HMGB1,VEGF和PCNA的表达显着增加,血管内皮内皮细胞加速,血清TNF-α和CRP水平降低。被adGFP-HMGB1感染的MSC的移植增强了MSC的作用。综上所述,HMGB1的修饰可以通过上调VEGF和PCNA的表达并抑制炎症反应来增强MSC对球囊诱发的颈动脉损伤的保护作用。 MSC中的HMGB1可能代表了内皮修复的新型治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号