Getwan Maike, Lienkamp Soeren S
Department of Medicine, Renal Division, Medical Center-Faculty of Medicine, University of Freiburg, Hugstetter Str. 55, 79106, Freiburg, Germany.
BIOSS Centre of Biological Signalling Studies, University of Freiburg, Schänzlestr. 18, 79104, Freiburg, Germany.
Cell Tissue Res. 2017 Jul;369(1):143-157. doi: 10.1007/s00441-017-2611-2. Epub 2017 Apr 11.
Xenopus is a versatile model organism increasingly used to study organogenesis and genetic diseases. The rapid embryonic development, targeted injections, loss- and gain-of-function experiments and an increasing supply of tools for functional in vivo analysis are unique advantages of the Xenopus system. Here, we review the vast array of methods available that have facilitated its transition into a translational model. We will focus primarily on how these methods have been employed in the study of kidney development, renal function and kidney disease. Future advances in the fields of genome editing, imaging and quantitative 'omics approaches are likely to enable exciting and novel applications for Xenopus to deepen our understanding of core principles of renal development and molecular mechanisms of human kidney disease. Thus, using Xenopus in clinically relevant research diversifies the narrowing pool of "standard" model organisms and provides unique opportunities for translational research.
非洲爪蟾是一种用途广泛的模式生物,越来越多地用于研究器官发生和遗传疾病。非洲爪蟾系统的独特优势包括胚胎发育迅速、靶向注射、功能丧失和功能获得实验,以及用于体内功能分析的工具供应不断增加。在这里,我们回顾了大量可用的方法,这些方法促进了它向转化模型的转变。我们将主要关注这些方法如何应用于肾脏发育、肾功能和肾脏疾病的研究。基因组编辑、成像和定量“组学”方法领域的未来进展可能会为非洲爪蟾带来令人兴奋的新应用,以加深我们对肾脏发育核心原理和人类肾脏疾病分子机制的理解。因此,在临床相关研究中使用非洲爪蟾使日益狭窄的“标准”模式生物库更加多样化,并为转化研究提供了独特的机会。