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A nephron model for study of drug-induced acute kidney injury and assessment of drug-induced nephrotoxicity

机译:一种用于研究药物诱导的急性肾损伤的肾功能术语和药物诱导的肾毒性评估

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摘要

Abstract In this study, we developed a multilayer microfluidic device to simulate nephron, which was formed by “glomerulus”, “Bowman's capsule”, “proximal tubular lumen” and “peritubular capillary”. In this microdevice, artificial renal blood flow was circulating and glomerular filtrate flow was single passing through, mimicking the behavior of a nephron. In this dynamic artificial nephron, we observed typical renal physiology, including the glomerular size-selective barrier, glomerular basement membrane charge-selective barrier, glucose reabsorption and para-aminohippuric acid secretion. To demonstrate the capability of our microdevice, we used it to investigate the pathophysiology of drug-induced acute kidney injury (AKI) and give assessment of drug-induced nephrotoxicity, with cisplatin and doxorubicin as model drugs. In the experiment, we loaded the doxorubicin or cisplatin in the “renal blood flow”, recorded the injury of primary glomerular endothelial cells, podocytes, tubular epithelial cells and peritubular endothelial cells by fluorescence imaging, and identified the time-dependence, dose-dependence and the death order of four types of renal cells. Then by measuring multiple biomarkers, including E-cadherin, VEGF, VCAM-1, Nephrin, and ZO-1, we studied the mechanism of cell injuries caused by doxorubicin or cisplatin. Also, we investigated the effect of BSA in the “renal blood flow” on doxorubicin-or-cisplatin-induced nephrotoxicity, and found that BSA enhanced the tight junctions between cells and eased cisplatin-induced nephrotoxicity. In addition, we compared the nephron model and traditional tubule models for assessment of drug-induced nephrotoxicity. And it can be inferred that our biomimetic microdevice simulated the complex, dynamic microenvironment of nephron, yielded abundant information about drug-induced-AKI at the preclinical stage, boosted the drug safety evaluation, and provided a reliable reference for clinical therapy.
机译:摘要在这项研究中,我们开发了一种多层微流体装置来模拟肾上的肾,其由“肾小球”,“鲍曼胶囊”,“近端管状腔”和“梗塞毛细血管”形成。在这种微生物中,人工肾血流循环,并且肾小球滤液流单独通过,模仿肾的行为。在这种动态人工肾上腺中,我们观察到典型的肾生理学,包括肾小球尺寸选择性屏障,肾小球基底膜充电选择性屏障,葡萄糖重吸收和对氨基生物酸分泌。为了展示我们的微型方法的能力,我们使用它来研究药物诱导的急性肾损伤(AKI)的病理生理学,并评估药物诱导的肾毒性,使顺铂和多柔比蛋白作为模型药物。在实验中,我们在“肾血流”中加载了多柔比蛋白或顺铂,通过荧光成像记录了初级肾小球内皮细胞,翼细胞,管状上皮细胞和梗死内皮细胞的损伤,并确定了时间依赖性剂量依赖性和四种类型的肾细胞的死亡顺序。然后通过测量多种生物标志物,包括E-Cadherin,VEGF,VCAM-1,Nephrin和ZO-1,我们研究了由多柔比星或顺铂引起的细胞损伤机制。此外,我们研究了BSA在“肾血流量”对多柔比星或顺铂诱导的肾毒性的影响,发现BSA增强了细胞之间的紧密交界,缓解了顺铂诱导的肾毒性。此外,我们比较了肾上模型和传统小管模型,用于评估药物诱导的肾毒性。可以推断,我们的仿生微细胞模拟了肾脏的复杂,动态的微环境,在临床前阶段产生了有关药物诱导的含量的丰富信息,提高了药物安全评估,并为临床治疗提供了可靠的参考。

著录项

  • 来源
    《Biomaterials》 |2018年第2018期|共13页
  • 作者单位

    State Key Laboratory of Fine Chemicals Department of Chemical Engineering &

    School of;

    Institute of Cancer Stem Cell Dalian Medical University;

    State Key Laboratory of Fine Chemicals Department of Chemical Engineering &

    School of;

    Dalian Institute of Chemical Physics Chinese Academy of Sciences;

    College of Stomatology Dalian Medical University;

    State Key Laboratory of Fine Chemicals Department of Chemical Engineering &

    School of;

    State Key Laboratory of Fine Chemicals Department of Chemical Engineering &

    School of;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程;
  • 关键词

    Nephron; Microfluidics; AKI; Nephrotoxicity;

    机译:肾上;微流体;aki;肾毒性;

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