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首页> 外文期刊>Physiological Reports >A bell‐shaped pattern of urinary aquaporin‐2‐bearing extracellular vesicle release in an experimental model of nephronophthisis
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A bell‐shaped pattern of urinary aquaporin‐2‐bearing extracellular vesicle release in an experimental model of nephronophthisis

机译:肾小球肾炎的实验模型中呈铃状的尿液中含有水通道蛋白2的细胞外囊泡释放

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The DBA/2‐FG pcy (pcy) mouse is a model of human nephronophthisis, a recessive cystic kidney disease. Renal expression of aquaporin‐2 (AQP2), a water channel protein, has been shown to be altered in pcy mice. However, the relationship between the renal expression and its release in urinary extracellular vesicles (uEV‐AQP2), which account for most urinary AQP2, in pcy mice has remained largely unknown. In this study, we examined age‐related alterations of this relationship in pcy mice. In comparison with control mice, pcy mice after the age of 14?weeks showed defective urinary concentration ability with an increase in urinary volume. Interestingly, the release of uEV‐AQP2 increased progressively up to the age of 16?weeks, but at 21?weeks the release did not significantly differ from that in control mice (i.e., a bell‐shaped pattern was evident). Similar results were obtained for uEV marker proteins, including tumor susceptibility gene 101 (TSG101) protein and apoptosis‐linked gene 2‐interacting protein X (Alix). Immunoblot analysis revealed that renal AQP2 expression increased progressively from 11?weeks, and immunohistochemistry showed that this increase was possibly due to an increase in the number of AQP2‐positive cells. Analysis of mRNAs for seven types of AQP expressed in the kidney supported this notion. These data suggest that the level of uEV‐AQP2 does not simply mirror the renal expression of AQP2 and that the altered release of uEV‐AQP2 in pcy mice depends on the numbers of both renal AQP2‐positive cells and EVs released into the urine.
机译:DBA / 2-FG pcy(pcy)小鼠是人类肾炎的一种模型,这是一种隐性的囊性肾脏疾病。水通道蛋白Aquaporin-2(AQP2)的肾脏表达已在pcy小鼠中改变。然而,在pcy小鼠中,肾表达与其在尿液外囊泡(uEV-AQP2)中的释放之间的关系仍然很不明确,uEV-AQP2占尿液AQP2的大部分。在这项研究中,我们检查了pcy小鼠中这种关系的年龄相关变化。与对照小鼠相比,在14周后的pcy小鼠尿液浓缩能力下降,尿量增加。有趣的是,直到16周时,uEV-AQP2的释放逐渐增加,但是在21周时,其释放与对照组相比没有显着差异(即明显呈钟形)。 uEV标记蛋白也获得了相似的结果,包括肿瘤易感基因101(TSG101)蛋白和凋亡相关基因2相互作用蛋白X(Alix)。免疫印迹分析显示,肾脏AQP2表达从11周开始逐渐增加,免疫组织化学表明,这种增加可能是由于AQP2阳性细胞数量增加所致。对肾脏中表达的七种AQP的mRNA的分析支持了这一观点。这些数据表明uEV‐AQP2的水平不仅仅反映AQP2的肾脏表达,而且uCy小鼠uEV‐AQP2释放的改变取决于肾脏AQP2阳性细胞和尿液中释放的EV数量。

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