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The Anti-Oxidative Role of Micro-Vesicles Derived from Human Wharton-Jelly Mesenchymal Stromal Cells through NOX2/gp91(phox) Suppression in Alleviating Renal Ischemia-Reperfusion Injury in Rats

机译:通过抑制NOX2 / gp91(phox)抑制人沃顿-果冻间质基质细胞衍生的微囊泡在减轻大鼠肾脏缺血再灌注损伤中的抗氧化作用。

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摘要

Oxidative stress is known as one of the main contributors in renal ischemia/reperfusion injury (IRI). Here we hypothesized that Micro-vesicles (MVs) derived from human Wharton Jelly mesenchymal stromal cells (hWJMSCs) could protect kidney against IRI through mitigating oxidative stress. MVs isolated from hWJMSCs conditioned medium were injected intravenously in rats immediately after unilateral kidney ischemia for 60 min. The animals were sacrificed at 24h, 48h and 2 weeks respectively after reperfusion. Our results show that the expression of NOX2 and reactive oxygen species (ROS) in injured kidney tissues was declined and the oxidative stress was alleviated in MVs group at 24h and 48h in parallel with the reduced apoptosis and enhanced proliferation of cells. IRI-initiated fibrosis was abrogated by MVs coincident with renal function amelioration at 2 weeks. NOX2 was also found down-regulated by MVs both in human umbilical vein endothelial cells (HUVEC) and NRK-52E cell line under hypoxia injury model in vitro. In conclusion, a single administration of hWJMSC-MVs might protect the kidney by alleviation of the oxidative stress in the early stage of kidney IRI through suppressing NOX2 expression. Moreover, it could reduce the fibrosis and improved renal function.
机译:氧化应激是肾脏缺血/再灌注损伤(IRI)的主要因素之一。在这里,我们假设,源自人沃顿氏果冻间充质基质细胞(hWJMSCs)的微囊泡(MVs)可以通过减轻氧化应激来保护肾脏抵抗IRI。从hWJMSCs条件培养基中分离的MV在单侧肾脏缺血60分钟后立即静脉内注射到大鼠中。再灌注后分别在24h,48h和2周处死动物。我们的研究结果表明,MVs组在24h和48h肾脏组织中NOX2和活性氧(ROS)的表达降低,氧化应激得到缓解,同时细胞凋亡减少,细胞增殖增强。在2周时,伴随肾功能改善的MV消除了IRI启动的纤维化。在体外缺氧损伤模型下,人脐静脉内皮细胞(HUVEC)和NRK-52E细胞系中的MV也均下调了NOX2。总之,单次施用hWJMSC-MVs可以通过抑制NOX2表达减轻肾脏IRI早期的氧化应激,从而保护肾脏。此外,它可以减少纤维化并改善肾功能。

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