Drummond I A, Majumdar A, Hentschel H, Elger M, Solnica-Krezel L, Schier A F, Neuhauss S C, Stemple D L, Zwartkruis F, Rangini Z, Driever W, Fishman M C
Renal Unit, Massachusetts General Hospital, Charlestown MA 02129, USA.
Development. 1998 Dec;125(23):4655-67. doi: 10.1242/dev.125.23.4655.
The zebrafish pronephric kidney provides a simplified model of nephron development and epithelial cell differentiation which is amenable to genetic analysis. The pronephros consists of two nephrons with fused glomeruli and paired pronephric tubules and ducts. Nephron formation occurs after the differentiation of the pronephric duct with both the glomeruli and tubules being derived from a nephron primordium. Fluorescent dextran injection experiments demonstrate that vascularization of the zebrafish pronephros and the onset of glomerular filtration occurs between 40 and 48 hpf. We isolated fifteen recessive mutations that affect development of the pronephros. All have visible cysts in place of the pronephric tubule at 2-2.5 days of development. Mutants were grouped in three classes: (1) a group of twelve mutants with defects in body axis curvature and manifesting the most rapid and severe cyst formation involving the glomerulus, tubule and duct, (2) the fleer mutation with distended glomerular capillary loops and cystic tubules, and (3) the mutation pao pao tang with a normal glomerulus and cysts limited to the pronephric tubules. double bubble was analyzed as a representative of mutations that perturb the entire length of the pronephros and body axis curvature. Cyst formation begins in the glomerulus at 40 hpf at the time when glomerular filtration is established suggesting a defect associated with the onset of pronephric function. Basolateral membrane protein targeting in the pronephric duct epithelial cells is also severely affected, suggesting a failure in terminal epithelial cell differentiation and alterations in electrolyte transport. These studies reveal the similarity of normal pronephric development to kidney organogenesis in all vertebrates and allow for a genetic dissection of genes needed to establish the earliest renal function.
斑马鱼的前肾提供了一个简化的肾单位发育和上皮细胞分化模型,适用于遗传分析。前肾由两个带有融合肾小球以及成对的前肾小管和导管的肾单位组成。肾单位的形成发生在前肾导管分化之后,肾小球和肾小管均源自肾单位原基。荧光葡聚糖注射实验表明,斑马鱼前肾的血管生成和肾小球滤过的开始发生在受精后40至48小时。我们分离出了15个影响前肾发育的隐性突变。在发育2至2.5天时,所有突变体的前肾小管部位都出现了可见的囊肿。突变体分为三类:(1)一组12个突变体,其体轴弯曲存在缺陷,表现出涉及肾小球、肾小管和导管的最快速且严重的囊肿形成;(2)fleer突变体,其肾小球毛细血管环扩张且肾小管呈囊性;(3)pao pao tang突变体,其肾小球正常,囊肿仅限于前肾小管。对double bubble突变体进行了分析,它是扰乱整个前肾长度和体轴弯曲的突变的代表。囊肿形成在受精后40小时肾小球滤过建立时开始于肾小球,这表明存在与前肾功能开始相关的缺陷。前肾导管上皮细胞的基底外侧膜蛋白靶向也受到严重影响,这表明终末上皮细胞分化失败以及电解质转运发生改变。这些研究揭示了正常前肾发育与所有脊椎动物肾脏器官发生的相似性,并允许对建立最早肾功能所需的基因进行遗传剖析。