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首页> 外文期刊>Cell transplantation >The Cytoprotective Effects of Human Endothelial Progenitor Cell-Conditioned Medium Against an Ischemic Insult Are Not Dependent on VEGF and IL-8
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The Cytoprotective Effects of Human Endothelial Progenitor Cell-Conditioned Medium Against an Ischemic Insult Are Not Dependent on VEGF and IL-8

机译:人内皮祖细胞条件培养基对缺血性损伤的细胞保护作用并不依赖于VEGF和IL-8

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摘要

Endothelial progenitor cells (EPCs) promote revascularization and tissue repair mainly by paracrine actions. In the present study, we investigated whether EPC-secreted factors in the form of conditioned medium (EPC-CM) can protect cultured brain microvascular endothelial cells against an ischemic insult. Furthermore, we addressed the type of factors that are involved in the EPC-CM-mediated functions. For that purpose, rat brain-derived endothelial cells (rBCEC4 cell line) were exposed to EPC-CM pretreated with proteolytic digestion, heat inactivation, and lipid extraction. Moreover, the involvement of VEGF and IL-8, as canonical angiogenic factors, was investigated by means of neutralizing antibodies. We demonstrated that EPC-CM significantly protected the rBCEC4 cells against an ischemic insult mimicked by induced oxygen glucose deprivation followed by reoxygenation. The cytoprotective effect was displayed by higher viable cell numbers and reduced caspase 3/7 activity. Heat inactivation, proteolytic digestion, and lipid extraction resulted in a significantly reduced EPC-CM-dependent increase in rBCEC4 viability, tube formation, and survival following the ischemic challenge. Notably, VEGF and IL-8 neutralization did not affect the actions of EPC-CM on rBCEC4 under both standard and ischemic conditions. In summary, our findings show that paracrine factors released by EPCs activate an angiogenic and cytoprotective response on brain microvascular cells and that the activity of EPC-CM relies on the concerted action of nonproteinaceous and proteinaceous factors but do not directly involve VEGF and IL-8.
机译:内皮祖细胞(EPC)主要通过旁分泌作用促进血运重建和组织修复。在本研究中,我们调查了条件培养基(EPC-CM)形式的EPC分泌因子是否可以保护培养的脑微血管内皮细胞免受缺血性损伤。此外,我们讨论了EPC-CM介导的功能所涉及的因素类型。为此,将大鼠脑源性内皮细胞(rBCEC4细胞系)暴露于经过蛋白水解消化,热灭活和脂质提取预处理的EPC-CM中。此外,通过中和抗体研究了作为典型血管生成因子的VEGF和IL-8的参与。我们证明,EPC-CM显着保护rBCEC4细胞免受由诱导的氧葡萄糖剥夺然后再充氧模仿的缺血性损伤。通过较高的活细胞数和降低的半胱天冬酶3/7活性来显示细胞保护作用。热失活,蛋白水解消化和脂质提取导致缺血挑战后,rBCEC4活力,管形成和存活的EPC-CM依赖性增加显着降低。值得注意的是,在标准和缺血条件下,VEGF和IL-8的中和作用均不影响EPC-CM对rBCEC4的作用。总之,我们的发现表明,EPC释放的旁分泌因子可激活脑微血管细胞的血管生成和细胞保护反应,而EPC-CM的活性依赖于非蛋白质和蛋白质因子的协同作用,但并不直接涉及VEGF和IL-8 。

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