蛋白尿性肾病中巨膜蛋白和立方蛋白在近端小管的表达模式
Proximal Tubular Expression Patterns of Megalin and Cubilin in Proteinuric Nephropathies.
作者信息
Sun Jia, Hultenby Kjell, Axelsson Jonas, Nordström Johan, He Bing, Wernerson Annika, Lindström Karin
机构信息
Division of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Division of Clinical Research Center, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
出版信息
Kidney Int Rep. 2017 Mar 1;2(4):721-732. doi: 10.1016/j.ekir.2017.02.012. eCollection 2017 Jul.
INTRODUCTION
Receptor-mediated endocytosis is responsible for protein reabsorption in the proximal tubules. For albumin this process involves at least 2 interacting receptors, megalin and cubilin. Albumin is not usually present in the urine, indicating a highly efficient tubular reuptake under physiological conditions. However, early appearance of albuminuria may mean that the tubular system is overwhelmed by large quantities of albumin or that the function is impaired.
METHODS
To better understand the physiological role of megalin and cubilin in human renal disease, renal biopsies from 15 patients with a range of albuminuria and 3 healthy living donors were analyzed for proximal tubular expression of megalin and cubilin using immunohistochemistry (IHC) and semiquantitative immune-electron microscopy. Their expression in proteinuric zebrafish was also studied.
RESULTS
Megalin and cubilin were expressed in brush border and cytoplasmic vesicles. Patients with microalbuminuric IgA nephropathy and thin membrane disease had significantly higher megalin in proximal tubules, whereas those with macro- or nephrotic-range albuminuria had unchanged levels. Cubilin expression was significantly higher in all patients. In a proteinuric zebrafish nphs2 knockdown model, we found a dose-dependent increase in the expression of tubular megalin and cubilin in response to tubular protein uptake.
DISCUSSION
Megalin and cubilin show different expression patterns in different human diseases, which indicates that the 2 tubular proteins differently cooperate in cleaning up plasma proteins in kidney tubules.
引言
受体介导的内吞作用负责近端小管中的蛋白质重吸收。对于白蛋白而言,这一过程至少涉及两种相互作用的受体,即巨膜蛋白和 cubilin。白蛋白通常不存在于尿液中,这表明在生理条件下肾小管具有高效的重吸收功能。然而,蛋白尿的早期出现可能意味着肾小管系统被大量白蛋白 overwhelm,或者其功能受损。
方法
为了更好地了解巨膜蛋白和 cubilin 在人类肾脏疾病中的生理作用,我们使用免疫组织化学(IHC)和半定量免疫电子显微镜对 15 例不同蛋白尿水平的患者以及 3 名健康活体供者的肾活检组织进行了巨膜蛋白和 cubilin 在近端小管表达的分析。我们还研究了它们在蛋白尿斑马鱼中的表达。
结果
巨膜蛋白和 cubilin 在刷状缘和细胞质小泡中表达。微量白蛋白尿型 IgA 肾病和薄基底膜肾病患者近端小管中的巨膜蛋白水平显著更高,而大量蛋白尿或肾病范围蛋白尿患者的巨膜蛋白水平未发生变化。所有患者的 cubilin 表达均显著更高。在蛋白尿斑马鱼 nphs2 基因敲低模型中,我们发现肾小管中巨膜蛋白和 cubilin 的表达随着肾小管蛋白摄取呈剂量依赖性增加。
讨论
巨膜蛋白和 cubilin 在不同人类疾病中表现出不同的表达模式,这表明这两种肾小管蛋白在清除肾小管中的血浆蛋白方面发挥着不同的协同作用。