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Renoprotective Effect of Human Umbilical Cord–Derived Mesenchymal Stem Cells in Immunodeficient Mice Suffering from Acute Kidney Injury

机译:人脐肾脏的保护作用脐血间充质干免疫缺陷小鼠痛苦细胞急性肾损伤

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摘要

It is unknown whether human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) can improve the renal function of patients suffering from acute kidney injury. Moreover, before beginning clinical trials, it is necessary to investigate this renoprotective effect of hUC-MSCs in a xenogeneic model of acute kidney injury. However, no previous studies have examined the application of hUC-MSCs to immunodeficient mice suffering from acute kidney injury. The objectives of this study were to examine whether hUC-MSCs could improve renal function in nonobese diabetic-severe combined immune deficiency (NOD-SCID) mice suffering from acute kidney injury, and to investigate the mechanism(s) for hUC-MSCs to improve renal function in this xenogeneic model. Early (3 hr) and late (12 hr) administrations of hUC-MSCs (106 cells) were performed via the external jugular vein into NOD-SCID mice suffering from either folic acid (FA) (250 mg/kg body weight) or vehicle. The results showed that early administration of hUC-MSCs improved the renal function of NOD-SCID mice suffering from FA-induced acute kidney injury, as evidenced by decreased serum urea nitrogen and serum creatinine levels, as well as a reduced tubular injury score. The beneficial effects of hUC-MSCs were through reducing apoptosis and promoting proliferation of renal tubular cells. These benefits were independent of inflammatory cytokine effects and transdifferentiation. Furthermore, this study is the first one to show that the reduced apoptosis of renal tubular cells by hUC-MSCs in this xenogeneic model is mediated through the mitochondrial pathway, and through the increase of Akt phosphorylation.
机译:尚不清楚人脐带间充质干细胞(hUC-MSC)是否可以改善患有急性肾损伤的患者的肾功能。此外,在开始临床试验之前,有必要在急性肾损伤的异种模型中研究hUC-MSC的这种肾脏保护作用。但是,以前没有研究检查过hUC-MSC在患有急性肾损伤的免疫缺陷小鼠中的应用。这项研究的目的是检查hUC-MSCs是否可以改善患有急性肾损伤的非肥胖糖尿病-重症合并免疫缺陷(NOD-SCID)小鼠的肾功能,并研究hUC-MSCs改善其机制该异种模型中的肾功能。通过颈外静脉将hUC-MSC(10 6 细胞)的早期(3 hr)和晚期(12 hr)给药到患有叶酸(FA)(250)的NOD-SCID小鼠中mg / kg体重)或媒介物。结果表明,早期给予hUC-MSC可改善FA诱导的急性肾损伤的NOD-SCID小鼠的肾功能,这可通过降低血清尿素氮和血清肌酐水平,以及降低肾小管损伤评分来证明。 hUC-MSC的有益作用是通过减少凋亡和促进肾小管细胞的增殖。这些益处与炎性细胞因子作用和转分化无关。此外,这项研究是第一个表明在这种异种模型中,hUC-MSCs减少肾小管细胞凋亡的途径是通过线粒体途径和通过增加Akt磷酸化介导的。

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