Division of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Department of Biomedical Engineering, Draper Laboratory, Cambridge, Massachusetts, USA.
Tissue Eng Part B Rev. 2022 Aug;28(4):938-948. doi: 10.1089/ten.TEB.2021.0154. Epub 2021 Dec 8.
Unraveling the complex behavior of healthy and disease podocytes by analyzing the changes in their unique arrangement of foot processes, slit diaphragm, and the three-dimensional (3D) morphology is a long-standing goal in kidney-glomerular research. The complexities surrounding the podocytes' accessibility in animal models and growing evidence of differences between humans and animal systems have compelled researchers to look for alternate approaches to study podocyte behaviors. With the advent of bioengineered models, an increasingly powerful and diverse set of tools is available to develop novel podocyte culture systems. This review discusses the pertinence of various culture models of podocytes to study podocyte mechanisms in both normal physiology and disease conditions. While no one system comprehensively recapitulates podocytes' architecture, we emphasize how the existing systems can be exploited to answer targeted questions on podocyte structure and function. We highlight the distinct advantages and limitations of using these models to study podocyte behaviors and screen therapeutics. Finally, we discuss various considerations and potential engineering strategies for developing next-generation complex 3D culture models for studying podocyte behaviors . Impact Statement In various glomerular kidney diseases, there are numerous alterations in podocyte structure and function. Yet, many of these disease events and the required targeted therapies remain unknown, resulting in nonspecific treatments. The scientific and clinical communities actively search for new modes to develop structurally and functionally relevant podocyte culture systems to gain insights into various diseases and develop therapeutics. Current systems help in some ways but are not sufficient. A deeper understanding of these previous approaches is essential to advance the field, and importantly, bioengineering strategies can contribute a unique toolbox to establish next-generation podocyte systems.
通过分析足细胞独特的足突、裂孔隔膜排列和三维(3D)形态的变化来揭示健康和患病足细胞的复杂行为,这是肾脏肾小球研究中的一个长期目标。由于动物模型中足细胞的可及性复杂,以及人类和动物系统之间存在差异的证据越来越多,研究人员不得不寻找替代方法来研究足细胞行为。随着生物工程模型的出现,越来越多的强大而多样化的工具可用于开发新型足细胞培养系统。本文讨论了各种足细胞培养模型在研究正常生理和疾病条件下足细胞机制的相关性。虽然没有一个系统能够全面再现足细胞的结构,但我们强调了如何利用现有系统来回答关于足细胞结构和功能的特定问题。我们突出了使用这些模型研究足细胞行为和筛选治疗方法的独特优势和局限性。最后,我们讨论了开发用于研究足细胞行为的下一代复杂 3D 培养模型的各种考虑因素和潜在工程策略。
影响说明在各种肾小球肾脏疾病中,足细胞的结构和功能发生了许多改变。然而,许多这些疾病事件和所需的靶向治疗仍然未知,导致治疗方法缺乏特异性。科学界和临床界积极寻求新的模式来开发具有结构和功能相关性的足细胞培养系统,以深入了解各种疾病并开发治疗方法。目前的系统在某些方面有所帮助,但还不够。深入了解这些先前的方法对于推动该领域的发展至关重要,重要的是,生物工程策略可以为建立下一代足细胞系统提供独特的工具包。