Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts; and Program in Membrane Biology and Division of Nephrology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts; and.
Am J Physiol Cell Physiol. 2014 Oct 1;307(7):C597-605. doi: 10.1152/ajpcell.00154.2014. Epub 2014 Jun 18.
A reduction or loss of plasma membrane aquaporin 2 (AQP2) in kidney principal cells due to defective vasopressin (VP) signaling through the VP receptor causes excessive urine production, i.e., diabetes insipidus. The amount of AQP2 on the plasma membrane is regulated by a balance of exocytosis and endocytosis and is the rate limiting step for water reabsorption in the collecting duct. We describe here a systematic approach using high-throughput screening (HTS) followed by in vitro and in vivo assays to discover novel compounds that enhance vasopressin-independent AQP2 membrane expression. We performed initial chemical library screening with a high-throughput exocytosis fluorescence assay using LLC-PK1 cells expressing soluble secreted yellow fluorescent protein and AQP2. Thirty-six candidate exocytosis enhancers were identified. These compounds were then rescreened in AQP2-expressing cells to determine their ability to increase AQP2 membrane accumulation. Effective drugs were then applied to kidney slices in vitro. Three compounds, AG-490, β-lapachone, and HA14-1 increased AQP2 membrane accumulation in LLC-PK1 cells, and both AG-490 and β-lapachone were also effective in MDCK cells and principal cells in rat kidney slices. Finally, one compound, AG-490 (an EGF receptor and JAK-2 kinase inhibitor), decreased urine volume and increased urine osmolality significantly in the first 2-4 h after a single injection into VP-deficient Brattleboro rats. In conclusion, we have developed a systematic procedure for identifying new compounds that modulate AQP2 trafficking using initial HTS followed by in vitro assays in cells and kidney slices, and concluding with in vivo testing in an animal model.
由于抗利尿激素(VP)信号通过 VP 受体的缺陷导致肾脏主细胞的质膜水通道蛋白 2(AQP2)减少或丧失,会导致过多的尿液产生,即尿崩症。质膜上 AQP2 的数量受胞吐作用和内吞作用的平衡调节,是集合管中水重吸收的限速步骤。我们在这里描述了一种使用高通量筛选(HTS)然后进行体外和体内测定的系统方法,以发现增强抗利尿激素非依赖性 AQP2 膜表达的新型化合物。我们使用表达可溶性分泌型黄色荧光蛋白和 AQP2 的 LLC-PK1 细胞进行了高内涵胞吐荧光测定的初始化学文库筛选。鉴定出 36 种候选的胞吐作用增强剂。然后,将这些化合物在表达 AQP2 的细胞中重新筛选,以确定它们增加 AQP2 膜积累的能力。有效的药物随后应用于体外的肾切片。三种化合物,AG-490、β-拉帕醌和 HA14-1,增加了 LLC-PK1 细胞中 AQP2 的膜积累,AG-490 和 β-拉帕醌在 MDCK 细胞和大鼠肾切片中的主细胞中也有效。最后,一种化合物,AG-490(一种表皮生长因子受体和 JAK-2 激酶抑制剂),在单次注射到 VP 缺乏的 Brattleboro 大鼠后 2-4 小时内显著减少尿量并增加尿渗透压。总之,我们已经开发了一种系统程序,用于使用初始 HTS 然后在细胞和肾切片中进行体外测定,最后在动物模型中进行体内测试来鉴定调节 AQP2 运输的新型化合物。