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Hypoxic preconditioning‐induced autophagy enhances survival of engrafted endothelial progenitor cells in ischaemic limb

机译:缺氧预处理诱导的自噬可提高缺血肢体中植入的内皮祖细胞的存活率

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摘要

Recent clinical studies have suggested that endothelial progenitor cells (EPCs) transplantation provides a modest benefit for treatment of the ischaemic diseases such as limb ischaemia. However, cell‐based therapies have been limited by poor survival of the engrafted cells. This investigation was designed to establish optimal hypoxia preconditioning and evaluate effects of hypoxic preconditioning‐induced autophagy on survival of the engrafted EPCs. Autophagy of CD34+ VEGFR‐2+ EPCs isolated from rat bone marrow increased after treatment with 1% O2. The number of the apoptotic cells in the hypoxic cells increased significantly after autophagy was inhibited with 3‐methyladenine. According to balance of autophagy and apoptosis, treatment with 1% O2 for 2 hrs was determined as optimal preconditioning for EPC transplantation. To examine survival of the hypoxic cells, the cells were implanted into the ischaemic pouch of the abdominal wall in rats. The number of the survived cells was greater in the hypoxic group. After the cells loaded with fibrin were transplanted with intramuscular injection, blood perfusion, arteriogenesis and angiogenesis in the ischaemic hindlimb were analysed with laser Doppler‐based perfusion measurement, angiogram and the density of the microvessels in histological sections, respectively. Repair of the ischaemic tissue was improved significantly in the hypoxic preconditioning group. Loading the cells with fibrin has cytoprotective effect on survival of the engrafted cells. These results suggest that activation of autophagy with hypoxic preconditioning is an optimizing strategy for EPC therapy of limb ischaemia.
机译:最近的临床研究表明,内皮祖细胞(EPC)移植为缺血性疾病(如肢体缺血)的治疗提供了适度的益处。但是,基于细胞的疗法受到移植细胞存活率低的限制。这项研究旨在建立最佳的缺氧预处理条件,并评估缺氧预处理诱导的自噬对移植的EPC存活的影响。用1%O2处理后,从大鼠骨髓中分离出的CD34 + VEGFR-2 + EPC的自噬增加。用3-甲基腺嘌呤抑制自噬后,低氧细胞中凋亡细胞的数量显着增加。根据自噬和细胞凋亡的平衡,确定1%O2处理2小时是EPC移植的最佳预处理。为了检查缺氧细胞的存活,将细胞植入大鼠腹壁的缺血小袋中。低氧组的存活细胞数量更多。肌肉注射移植有纤维蛋白的细胞后,分别通过基于激光多普勒的灌注测量,组织学切片中的血管造影和微血管密度分析缺血后肢的血液灌注,动脉生成和血管生成。缺氧预处理组缺血组织的修复明显改善。用纤维蛋白加载细胞对移植细胞的存活具有细胞保护作用。这些结果表明,缺氧预处理激活自噬是肢体缺血EPC治疗的一种优化策略。

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