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首页> 外文期刊>Experimental and therapeutic medicine >Delivery of biotinylated IGF-1 with biotinylated self-assembling peptides combined with bone marrow stem cell transplantation promotes cell therapy for myocardial infarction
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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:用生物素化的自组装肽递送生物素化IGF-1,与骨髓干细胞移植联合促进心肌梗死的细胞疗法

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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 similar to 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:细胞疗法是一种有希望的心脏修复方法。本研究的目的是通过将生物素化的胰岛素样生长因子1(IGF-1)与生物素化的自组装肽(系环化IGF-1)与骨髓干细胞(BMSCs)移植联系进行治疗的可行性心力衰竭。合成束缚IGF-1,分析其对H9C2细胞的影响。逆转录定量聚合酶链反应和蛋白质印迹测定表明,束缚IGF-1没有显着影响AKT的表达和磷酸化,而它显着增加了心肌肌钙蛋白T的表达(P <0.01)。构建兔心肌梗死模型,将兔子分为四组:对照组(无处理),第1组(G1; BMSC移植),第2组(G2; BMSCs +非生物素化IGF-1)和第3组(G3 ; BMSCs +系环IGF-1)。在建模后4周,获得心脏组织进行分析。在对照组中,心肌纤维紊乱,大量炎症细胞渗透到心脏组织,并且相似的细胞凋亡与50%相似。然而,在G1,G2和G3中,肌肉细胞被批量迅速,并且观察到较小程度的心肌变性和炎症细胞浸润。与对照组相比,G1-G3中心肌细胞的细胞凋亡率显着降低(P <0.01)。此外,与G1和G2相比,G3的组织形态得到改善,凋亡心肌细胞的数量显着降低(P <0.01)。这些结果表明,具有束缚IGF-1 + BMSC的处理显着抑制细胞凋亡并诱导心脏成熟蛋白的表达。这些调查结果提供了一种新颖的深入了解如何用BMSC递送束缚IGF-1可以提高心力衰竭治疗患者的预后。

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