首页> 外文期刊>Stem cells translational medicine. >Erythropoietin Stimulates Endothelial Progenitor Cells to Induce Endothelialization in an Aneurysm Neck After Coil Embolization by Modulating Vascular Endothelial Growth Factor
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Erythropoietin Stimulates Endothelial Progenitor Cells to Induce Endothelialization in an Aneurysm Neck After Coil Embolization by Modulating Vascular Endothelial Growth Factor

机译:促红细胞生成素通过调节血管内皮生长因子刺激线圈栓塞后在血管瘤颈中刺激内皮祖细胞诱导内皮化。

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This study explored a new approach to enhance aneurysm (AN) neck endothelialization via erythropoietin (EPO)-induced endothelial progenitor cell (EPC) stimulation. Results suggest that EPO enhanced the endothelialization of a coiled embolization AN neck by stimulating EPCs via vascular endothelial growth factor modulation. Thus, the promotion of endothelialization with EPO provides an additional therapeutic option for preventing the recurrence of ANs. Endovascular coil embolization is an attractive therapy for cerebral ANs, but recurrence is a main problem affecting long-term outcomes. In this study, we explored a new approach to enhance AN neck endothelialization via EPO-induced EPC stimulation. Ninety adult male Sprague-Dawley rats were selected for an in vivo assay, and 60 of them underwent microsurgery to create a coiled embolization AN model. The animals were treated with EPO, and endothelial repair was assessed via flow cytometry, immunofluorescence, electronic microscopy, cytokine detection, and routine blood work. EPO improved the viability, migration, cytokine modulation, and gene expression of bone marrow-derived EPCs and the results showed that EPO increased the number of circulating EPCs and improved endothelialization compared with untreated rats (p < .05). EPO had no significant effect on the routine blood work parameters. In addition, the immunofluorescence analysis showed that the number of KDR+ cells in the AN neck was elevated in the EPO-treated group (p < .05). Further study demonstrated that EPO promoted EPC viability and migration in vitro. The effects of EPO may be attributed to the modulation of vascular endothelial growth factor (VEGF). In particular, EPO enhanced the endothelialization of a coiled embolization AN neck by stimulating EPCs via VEGF modulation. Thus, the promotion of endothelialization with EPO provides an additional therapeutic option for preventing the recurrence of ANs.Erythropoietin (EPO) is involved in erythropoiesis and related conditions and is reported to enhance stem-cell mobilization from bone marrow while elevating stem-cell viability and function. In this study, EPO was also found to stimulate endothelial progenitor cells to induce the endothelialization of a coiled embolic aneurysm neck via vascular endothelial growth factor modulation. Endothelialization induction provides an additional therapeutic opportunity during vascular inner layer repair and remodeling. The results provide important information on the unique role EPO plays during vascular repair and remodeling.
机译:这项研究探索了通过促红细胞生成素(EPO)诱导的内皮祖细胞(EPC)刺激来增强动脉瘤(AN)颈动脉内皮化的新方法。结果表明,EPO通过血管内皮生长因子的调控刺激EPCs,从而增强了螺旋状栓塞AN颈部的内皮化。因此,用EPO促进内皮化为防止AN的复发提供了另外的治疗选择。血管内线圈栓塞术对脑AN是一种有吸引力的疗法,但复发是影响长期预后的主要问题。在这项研究中,我们探索了一种通过EPO诱导的EPC刺激增强AN颈部内皮化的新方法。选择了90只成年雄性Sprague-Dawley大鼠进行体内试验,其中60只接受了显微外科手术以创建螺旋栓塞AN模型。用EPO治疗动物,并通过流式细胞仪,免疫荧光,电子显微镜,细胞因子检测和常规血液检查评估内皮修复。 EPO改善了骨髓来源的EPC的活力,迁移,细胞因子调节和基因表达,结果表明,与未治疗的大鼠相比,EPO增加了循环EPC的数量并改善了内皮化作用(p <.05)。 EPO对常规血液工作参数无明显影响。此外,免疫荧光分析表明,在EPO处理组中,AN颈部的KDR +细胞数量增加了(p <.05)。进一步的研究表明,EPO促进了体外EPC的活力和迁移。 EPO的作用可能归因于血管内皮生长因子(VEGF)的调节。特别地,EPO通过经由VEGF调节刺激EPC来增强螺旋状栓塞AN颈部的内皮化。因此,EPO促进内皮化为防止ANs复发提供了另一种治疗选择。促红细胞生成素(EPO)参与促红细胞生成和相关疾病,据报道可增强骨髓的干细胞动员能力,同时提高干细胞的活力和功能。在这项研究中,还发现EPO可刺激内皮祖细胞通过血管内皮生长因子调节来诱导螺旋状栓塞动脉瘤颈的内皮化。血管内皮诱导在血管内层修复和重塑过程中提供了额外的治疗机会。这些结果提供了有关EPO在血管修复和重塑过程中发挥独特作用的重要信息。

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