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首页> 外文期刊>Journal of Advanced Pharmaceutical Technology Research >The enhancement apoptosis of osteosarcoma mesenchymal stem cells co-cultivation with peripheral blood mononuclear cells sensitized by secretome and granulocyte macrophage colony-stimulating factor
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The enhancement apoptosis of osteosarcoma mesenchymal stem cells co-cultivation with peripheral blood mononuclear cells sensitized by secretome and granulocyte macrophage colony-stimulating factor

机译:通过沉积物和粒细胞巨噬细胞菌落刺激因子致敏的外周血单核细胞综合培养骨质瘤间充质干细胞的增强凋亡

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摘要

The advanced, metastasis, and reccurent of osteosarcoma (OS) patients have a poor prognosis postaggresive surgery and chemotherapy. Peripheral blood mononuclear cells (PBMCs) as cell-based immunotherapy may successful in the OS treatment. To investigate the enhancement apoptosis of OS-mesenchymal stem cells (OS-MSCs) co-cultivated with PBMCs sensitized using the secretome and granulocyte macrophage colony-stimulating factor (GMCSF). This true experimental study with posttest only control group design and in vitro study. The sample was cultured OS-MSCs which confirmed by Cluster of Differentiation-133 using immunocytochemistry (ICC) and histopathology analysis. The sample divided into six groups accordingly: OS-MSC, OS-MSC + PMBC, OS-MSC + PMBC + Secretome, OS-MSC + PMBC + GMCSF, OS-MSC + PBMC + Secretome + GMCSF (n = 5/N = 30). The enhancement of OS-MSCs apoptosis was analyzed through Interleukin-2 (IL-2) level through the Enyzme-Linked Immunosorbent Assay examination, expression of Signal Transducers and Activators of Transcription (STAT)-3 and caspase-3 by ICC. One-way analysis of variance test and Tukey Honestly Significant Difference to analyze the difference between the groups (P 0.05). The highest of IL-2 level was found in the PBMC + Secretome + GMCSF group. The highest expression of caspase-3 was found in OS-MSC + PBMC + Secretome + GMCSF group with significant different between groups (P 0.05). There was insignificant difference of STAT-3 epxression and IL-2 level between groups (P 0.05). The co-cultivation of OS-MSCs and PBMSCs activated using secretome and GMCSF has a great ability to enhance OS-MSCs apoptosis.
机译:骨肉瘤(OS)患者的先进,转移和再循环患者预测性差异性差和化疗差。外周血单核细胞(PBMC)作为基于细胞的免疫疗法可能在OS治疗中取得成功。探讨用综合致敏的PBMC培养的OS-Mesenchyal干细胞(OS-MSCs)的增强细胞凋亡,所述PBMC使用综指和粒细胞巨噬细胞刺激因子(GMCSF)敏化。这种真正的实验研究与后塔控制组设计和体外研究。使用免疫细胞化学(ICC)和组织病理学分析,通过分化-133簇确认的培养OS-MSCs。相应地将样品分为六组:OS-MSC,OS-MSC + PMBC,OS-MSC + PMBC +秘密,OS-MSC + PMBC + GMCSF,OS-MSC + PBMC +秘密+ GMCSF(n = 5 / n = 30)。通过白细胞介素-2(IL-2)水平通过enyzME连接的免疫吸附测定检查,通过ICC的信号传感器和转录激活剂的表达(ICC的转录激活剂(STAT)-3和Caspase-3的激活剂分析OS-MSCs细胞凋亡的增强。方差试验的单向分析和簇生诚实地分析群体之间的差异(P <0.05)。在PBMC +秘密+ GMCSF组中发现了IL-2水平的最高。 Caspase-3的最高表达在OS-MSC + PBMC +批+ GMCSF组中发现,在组之间具有显着差异(P <0.05)。统计数据3 ePxression和IL-2之间存在微不足道的差异(P> 0.05)。使用局部和GMCSF激活OS-MSCs和PBMSCs的共培养具有较高的增强OS-MSCs细胞凋亡的能力。

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