Department of Medical Biochemistry and Biophysics, Karolinska Institutet, 171 77 Stockholm, Sweden.
J Am Soc Nephrol. 2011 Jun;22(6):1019-23. doi: 10.1681/ASN.2010121291. Epub 2011 May 12.
Podocytes do not remain fully differentiated when cultured, and they are difficult to image in vivo, making the study of podocyte biology challenging. Zebrafish embryos are transparent and develop a single, midline, pronephric glomerulus accessible for imaging and systematic functional analysis. Here, we describe a transgenic zebrafish line that expresses green fluorescence protein (GFP) from the zebrafish podocin promoter. The line recapitulates the endogenous pronephric podocin expression pattern, showing GFP expression exclusively in podocytes starting 2 days postfertilization. Using the podocyte GFP signal as a guide for dissection, we examined the pronephric glomerulus by scanning electron microscopy; the surface ultrastructure exhibited fine, interdigitating podocyte foot processes surrounding glomerular capillaries. To determine whether the GFP signal could serve as a direct readout of developmental abnormalities or injury to the glomerulus, we knocked down the podocyte-associated protein crb2b; this led to a loss of GFP signal. Thus, podocin-GFP zebrafish provide a model for ultrastructural studies and in vivo visualization and functional analysis of glomerular podocytes. This model should also be useful for high-throughput genetic or chemical analysis of glomerular development and function.
足细胞在培养时不会完全分化,并且在体内难以成像,这使得对足细胞生物学的研究具有挑战性。斑马鱼胚胎是透明的,并且发育出一个单一的、中线的、中肾肾小球,可用于成像和系统的功能分析。在这里,我们描述了一种表达绿色荧光蛋白(GFP)的转基因斑马鱼系,该蛋白由斑马鱼足细胞启动子驱动表达。该系重现了内源性中肾足细胞的表达模式,在受精后 2 天开始仅在足细胞中表达 GFP。我们使用足细胞 GFP 信号作为解剖的指导,通过扫描电子显微镜检查中肾肾小球;表面超微结构显示出精细的、相互交错的足细胞足突围绕着肾小球毛细血管。为了确定 GFP 信号是否可以作为肾小球发育异常或损伤的直接读出信号,我们敲低了与足细胞相关的蛋白 crb2b;这导致 GFP 信号的丢失。因此,足细胞 GFP 斑马鱼为肾小球足细胞的超微结构研究以及体内可视化和功能分析提供了一个模型。该模型也应该对肾小球发育和功能的高通量遗传或化学分析有用。