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Experimental Models to Study Podocyte Biology: Stock-Taking the Toolbox of Glomerular Research

机译:研究足细胞生物学的实验模型:评估肾小球研究工具箱

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摘要

Diseases affecting the glomeruli of the kidney, the renal filtration units, are a leading cause of chronic kidney disease and end-stage renal failure. Despite recent advances in the understanding of glomerular biology, treatment of these disorders has remained extraordinarily challenging in many cases. The use of experimental models has proven invaluable to study renal, and in particular, glomerular biology and disease. Over the past 15 years, studies identified different and very distinct pathogenic mechanisms that result in damage, loss of glomerular visceral epithelial cells (podocytes) and progressive renal disease. However, animal studies and, in particular, mouse studies are often protracted and cumbersome due to the long reproductive cycle and high keeping costs. Transgenic and heterologous expression models have been speeded-up by novel gene editing techniques, yet they still take months. In addition, given the complex cellular biology of the filtration barrier, certain questions may not be directly addressed using mouse models due to the limited accessibility of podocytes for analysis and imaging. In this review, we will describe alternative models to study podocyte biology experimentally. We specifically discuss current podocyte cell culture models, their role in experimental strategies to analyze pathophysiologic mechanisms as well as limitations with regard to transferability of results. We introduce current models in Caenorhabditis elegans, Drosophila melanogaster, and Danio rerio that allow for analysis of protein interactions, and principle signaling pathways in functional biological structures, and enable high-throughput transgenic expression or compound screens in multicellular organisms.
机译:影响肾脏肾小球(肾脏滤过单元)的疾病是慢性肾脏疾病和终末期肾衰竭的主要原因。尽管最近在肾小球生物学的理解上取得了进步,但是在许多情况下,对这些疾病的治疗仍然具有极大的挑战性。实验模型的使用已被证明对研究肾脏,尤其是肾小球生物学和疾病具有不可估量的价值。在过去的15年中,研究发现了不同且非常不同的致病机制,这些机制导致了损害,肾小球内脏上皮细胞(足细胞)丢失和进行性肾脏疾病。然而,由于长的生殖周期和高的饲养成本,动物研究,尤其是小鼠研究通常是长期的且繁琐的。新型基因编辑技术已加快了转基因和异源表达模型的开发,但仍需花费数月的时间。此外,鉴于过滤屏障的复杂细胞生物学特性,由于足细胞对分析和成像的可及性有限,某些问题可能无法使用小鼠模型直接解决。在这篇综述中,我们将描述通过实验研究足细胞生物学的替代模型。我们专门讨论当前的足细胞培养模型,它们在分析病理生理机制的实验策略中的作用以及对结果转移性的限制。我们在秀丽隐杆线虫,果蝇,果蝇中引入当前模型,这些模型可用于分析蛋白质相互作用以及功能性生物结构中的主要信号传导途径,并能在多细胞生物中实现高通量转基因表达或化合物筛选。

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