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Exosomes Derived From Mesenchymal Stem Cells Ameliorate Renal Ischemic-Reperfusion Injury Through Inhibiting Inflammation and Cell Apoptosis

机译:通过抑制炎症和细胞凋亡来源于间充质干细胞的外泌体来改善肾缺血再灌注损伤

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This study aimed to investigate the underlying mechanism of mesenchymal stem cells (MSCs) on protection of renal ischemia reperfusion injury (IRI). Exosomes originated from MSCs (MSC-ex) were extracted according to the instructions of Total Exosome Isolation Reagent. Rats were divided into five groups: sham-operated, IRI, MSC, MSC-ex, and MSC-ex + RNAase group. MSCs or MSC-ex were injected via carotid artery. The renal function test and pathological detection were applied to determine the renoprotection of MSC-ex on IRI. Western blotting and quantitative reverse transcription polymerase chain reaction (RT-qPCR) were conducted to examine the levels of apoptosis-related proteins and inflammatory cytokines. Our results revealed that MSC-derived exosomes attenuated renal dysfunction, histologic damage, and decreased apoptosis. The expression levels of inflammatory cytokines, such as interleukin 6 (IL-6), tumor necrosis factor-α (TNF-α), nuclear factor kappa B (NF-κB), and interferon gamma (IFN-γ), were decreased by the MSC-ex treatment. The expression levels of caspase-9, cleaved caspase-3, Bax, and Bcl-2 caused by IR were also inhibited by MSC-ex. MSC-ex + RNAase group shared the similar pattern of changes with IRI group, likely due to the ability of RNA hydrolase to eliminate the function of exosomes. Our results demonstrated that exosomes originating from MSCs have protective effects on IRI via inhibiting cell apoptosis and inflammatory responses. Out findings may provide a new insight into therapeutic mechanism of MSCs on renal IRI.
机译:本研究旨在探讨间充质干细胞(MSCS)对肾缺血再灌注损伤(IRI)保护的潜在机制。根据全外分离试剂的说明,提取来自MSCs(MSC-ex)的外泌体。大鼠分为五组:假手术,IRI,MSC,MSC-EX和MSC-EX + RNA酶组。通过颈动脉注射MSCs或MSC-ex。应用肾功能试验和病理检测来确定IRI上MSC-ex的再压保护。进行蛋白质印迹和定量逆转录聚合酶链反应(RT-QPCR)以检查凋亡相关蛋白质和炎性细胞因子的水平。我们的研究结果表明,MSC衍生的外泌体减弱了肾功能紊乱,组织学损伤,细胞凋亡降低。炎症细胞因子的表达水平,例如白细胞介素6(IL-6),肿瘤坏死因子-α(TNF-α),核因子Kappa(NF-κB)和干扰素γ(IFN-γ)减少MSC-EX治疗。 Caspase-9的表达水平,由IR引起的Caspase-9,切割的Caspase-3,Bax和Bcl-2的表达水平也被MSC-ex抑制。 MSC-EX + RNA酶组与IRI组共享类似的变化模式,可能是由于RNA水解酶消除外来肌肉功能的能力。我们的结果表明,源自MSCs的外虫物体通过抑制细胞凋亡和炎症反应对IRI具有保护作用。结果可能对MSCS对肾IRI的治疗机制提供了新的洞察。

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