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Delivery of biotinylated IGF-1 with biotinylated self-assembling peptides combined with bone marrow stem cell transplantation promotes cell therapy for myocardial infarction

机译:结合生物素化自组装肽的生物素化IGF-1的输送与骨髓干细胞移植的结合促进了心肌梗死的细胞治疗

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摘要

Cell therapy is a promising approach for cardiac repair. The aim of the present study was to determine the feasibility of using biotinylated insulin-like growth factor 1 (IGF-1) with biotinylated self-assembling peptides (tethered IGF-1) combined with bone marrow stem cells (BMSCs) transplantation for the treatment of heart failure. Tethered IGF-1 was synthesized and its effect on H9c2 cells was analyzed. Reverse transcription-quantitative polymerase chain reaction and western blot assays demonstrated that tethered IGF-1 did not significantly affect the expression and phosphorylation of AKT, whereas it significantly increased the expression of cardiac troponin T (P<0.01). A rabbit myocardial infarction model was constructed and rabbits were divided into four groups: Control group (no treatment), group 1 (G1; BMSC transplantation), group 2 (G2; BMSCs + non-biotinylated IGF-1) and group 3 (G3; BMSCs + tethered IGF-1). At 4 weeks after modeling, cardiac tissues were obtained for analysis. In the control group, myocardial fibers were disordered, a large number of inflammatory cells infiltrated the cardiac tissues, and apoptosis occurred in ~50% of cells. However, in G1, G2 and G3, muscle cells were well ordered, and a lesser degree of myocardial degeneration and inflammatory cell infiltration was observed. Compared with the control group, the apoptosis rates of myocardial cells in G1-G3 were significantly decreased (P<0.01). Furthermore, compared with G1 and G2, tissue morphology was improved in G3and the number of apoptotic myocardial cells was significantly decreased (P<0.01). These results suggest that treatment with tethered IGF-1 + BMSCs significantly suppresses cell apoptosis and induces the expression of cardiac maturation proteins. These findings provide a novel insight into how the delivery of tethered IGF-1 with BMSCs could potentially enhance the prognosis of patients with heart failure treatment.
机译:细胞疗法是一种有前途的心脏修复方法。本研究的目的是确定将生物素化胰岛素样生长因子1(IGF-1)与生物素化自组装肽(拴系IGF-1)结合骨髓干细胞(BMSCs)移植治疗的可行性。心力衰竭。合成了拴系的IGF-1,并分析了其对H9c2细胞的作用。逆转录定量聚合酶链反应和蛋白质印迹实验表明,拴系的IGF-1不会显着影响AKT的表达和磷酸化,而会显着增加心肌肌钙蛋白T的表达(P <0.01)。构建了兔心肌梗塞模型,将兔分为四组:对照组(不治疗),第1组(G1; BMSC移植),第2组(G2; BMSCs +非生物素化的IGF-1)和第3组(G3) ; BMSCs +系留的IGF-1)。建模后第4周,获取心脏组织进行分析。在对照组中,心肌纤维紊乱,大量炎性细胞渗入心脏组织,约50%的细胞发生凋亡。然而,在G1,G2和G3中,肌肉细胞排列良好,并且观察到程度较小的心肌变性和炎性细胞浸润。与对照组相比,G1-G3心肌细胞凋亡率明显降低(P <0.01)。此外,与G1和G2相比,G3的组织形态得到改善,凋亡的心肌细胞数量明显减少(P <0.01)。这些结果表明,用束缚的IGF-1 + BMSCs处理可显着抑制细胞凋亡并诱导心脏成熟蛋白的表达。这些发现提供了关于如何将束缚的IGF-1与BMSC一起递送的新见解,可以潜在地改善心力衰竭患者的预后。

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