骨髓间充质干细胞移植可促进移植胰岛周围新生血管形成

Effect of bone mesenchymal stem cell transplantation on accelerating the vascularization surrounding transplant pancreatic islet

  • 摘要:
      目的  探讨胰岛移植联合骨髓间充质干细胞(MSC)移植能否促进移植胰岛周围新生血管形成。
      方法  以非肥胖糖尿病(NOD)小鼠作为受体,将NOD小鼠随机分为4组,联合移植组(6只)、单独胰岛移植组(6只)、单独MSC移植组(6只)、假性移植组(3只)。观察各组NOD小鼠移植后血糖和存活率的变化;采用5-乙炔基-2’脱氧尿苷(EdU)及dUTP缺口末端标记(TUNEL)方法,在胰岛移植后1、2、4周检测单独胰岛移植组和联合移植组移植胰岛的增殖与凋亡情况;采用光学显微镜(光镜)直接观察、组织化学及免疫组化的方法观察并定量分析,移植术后2、4、8周单独胰岛移植组和联合移植组移植胰岛的周围新生血管密度。
      结果  MSC联合移植与胰岛单独移植均能明显改善移植后小鼠的血糖水平,提高NOD小鼠的存活率。MSC联合移植可促进胰岛细胞再生,减少细胞凋亡。联合移植组移植胰岛周围血管密度明显大于单独胰岛移植组。
      结论  MSC可以促进移植胰岛周围新生血管生成,增加移植胰岛的血供,保护移植胰岛的功能与活性。

     

    Abstract:
      Objective  To investigate whether pancreatic islet transplantation in combination with bone mesenchymal stem cells (MSC) transplantation can promote the vascularization surrounding the transplant pancreatic islet.
      Methods  The non-obese diabetic (NOD) mice were utilized as the recipients and randomly divided into pancreatic islet transplantation combined with MSC transplantation group (co-transplantation group, n=6), pancreatic islet transplantation group (n=6), MSC transplantation group (n=6) and sham transplantation group (n=3). The variation in blood glucose level and survival rate post-transplantation of NOD mice in each group was observed. The proliferation and apoptosis of the transplant pancreatic islet in the pancreatic islet transplantation group and co-transplantation group at 1, 2 and 4 weeks after pancreatic islet transplantation were analyzed by 5-ethynyl-2'-deoxyuridine (EdU) and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL). The vascular density surrounding the transplanted pancreatic islet in the pancreatic islet transplantation group and co-transplantation group at postoperative 2, 4 and 8 weeks were observed under light microscope and quantitatively analyzed by histochemical and immunohistochemical staining.
      Results  Both MSC combined with pancreatic islet transplantation and pancreatic islet transplantation significantly improved the blood glucose level and enhanced the survival rate of NOD mouse models after transplantation. In addition, it could accelerate the regeneration of pancreatic islet cells and decrease cell apoptosis. MSC combined with pancreatic islet transplantation significantly enhanced the vascular density surrounding the transplant pancreatic islet compared with pancreatic islet transplantation alone.
      Conclusions  MSC transplantation can accelerate the vascularization surrounding the transplant pancreatic islet, increase the blood supply and protect the function and activity of the transplant pancreatic islet.

     

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