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微生理肾小球滤过屏障:当前见解、创新与未来应用

Microphysiological Glomerular Filtration Barriers: Current Insights, Innovations, and Future Applications.

作者信息

Miran Manon, Ngo Kieu, Buob David, Debiec Hanna, Ronco Pierre, Perry Guillaume

机构信息

Sorbonne Université, Inserm, Common and Rare Kidney Diseases: from Molecular Events to Precision Medicine, CoRaKiD, Paris, F-75020, France.

Sorbonne Université, CNRS, Laboratoire de Réactivité de Surface, LRS, Paris, F-75005, France.

出版信息

Adv Biol (Weinh). 2025 Sep;9(9):e00108. doi: 10.1002/adbi.202500108. Epub 2025 Jul 7.

Abstract

Chronic kidney disease (CKD) affects over 850 million individuals worldwide, often progressing to stages requiring dialysis or kidney transplants. Central to kidney function is the glomerular filtration barrier (GFB), which selectively filters waste while retaining essential proteins. Traditional models, including animal studies and 2D cell cultures, fail to fully replicate the GFB's complexity, limiting CKD research. Recent developments in microphysiological systems (MPS), particularly microphysiological glomerular filtration barriers (MPGFB), provide more accurate in vitro models for studying kidney diseases and evaluating therapies. MPGFB systems use organ-on-chip technology to integrate podocytes and glomerular endothelial cells within confined microfluidic environments, closely mimicking GFB's dynamic in vivo conditions. This setup enables detailed permeability analysis, aiding in research on disease mechanisms and drug toxicity. Furthermore, using human-induced pluripotent stem cells in MPGFB platforms allows patient-specific studies, enhancing insights into genetic kidney disorders. This review first examines the GFB's structure and function, focusing on its cellular and extracellular matrix components. It then discusses biological and engineering approaches to MPGFB fabrication, covering materials, 3D design, and flow control. The review concludes with MPGFB applications in disease modeling and drug testing, and addresses improvements needed for refining MPGFB as a key tool in kidney disease research and treatment.

摘要

慢性肾脏病(CKD)影响着全球超过8.5亿人,常常会发展到需要透析或肾移植的阶段。肾小球滤过屏障(GFB)是肾功能的核心,它能选择性地滤过废物,同时保留重要蛋白质。包括动物研究和二维细胞培养在内的传统模型无法完全复制GFB的复杂性,限制了CKD研究。微生理系统(MPS),特别是微生理肾小球滤过屏障(MPGFB)的最新进展,为研究肾脏疾病和评估治疗方法提供了更精确的体外模型。MPGFB系统利用芯片器官技术,将足细胞和肾小球内皮细胞整合到受限的微流体环境中,紧密模拟GFB在体内的动态条件。这种设置能够进行详细的通透性分析,有助于疾病机制和药物毒性的研究。此外,在MPGFB平台中使用人类诱导多能干细胞可以进行针对患者的研究,增强对遗传性肾脏疾病的认识。本综述首先考察GFB的结构和功能,重点关注其细胞和细胞外基质成分。然后讨论MPGFB制造的生物学和工程方法,涵盖材料、三维设计和流量控制。综述最后介绍了MPGFB在疾病建模和药物测试中的应用,并探讨了将MPGFB完善为肾脏疾病研究和治疗关键工具所需的改进措施。

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