Ludwig-Peitsch Wiebke K
Department of Dermatology, Vivantes Klinikum im Friedrichshain, Landsberger Allee 49, 10249, Berlin, Germany.
Adv Exp Med Biol. 2017;1006:337-345. doi: 10.1007/978-4-431-56550-5_20.
The central function of renal glomeruli is plasma ultrafiltration for primary urine production. The glomerular filtration barrier consists of a fenestrated endothelium, the glomerular basement membrane and podocytes, mesenchymal-like cells with actin filament-rich protrusions, the "foot processes." Their architecture and function are maintained and regulated by actin and several actin-binding proteins, mutations of which can be causative of glomerular diseases. Since initial immunostaining experiments had demonstrated intense drebrin reactions in renal glomeruli, the distribution of this protein was studied in detail in the kidneys of diverse mammalian species. Double-label confocal laser scanning microscopy revealed drebrin enrichment in mesangial cells of human, bovine, murine, and rat kidneys. In Thy-1.1 nephritic rat glomeruli, the protein was concentrated in mesangial cell processes and upregulated during their formation and remodeling. In adult human and bovine kidneys, drebrin was additionally accumulated in the foot processes of podocytes, a finding confirmed by immunoelectron microscopy. By contrast, podocytes of rodent glomeruli contained significant amounts of drebrin only during early developmental stages. In cultured murine podocytes induced to form cell processes, however, drebrin was concentrated in these protrusions, partly in colocalization with other actin-binding proteins. Protein extracts from human and bovine kidneys comprised 20 S-complexes of drebrin and actin, so-called drebrosomes. In summary, drebrin has to be added to the list of actin-binding proteins regulating actin dynamics of mesangial cell processes and foot processes of podocytes. It will be important to determine its role in hereditary and acquired glomerulopathies.
肾小球的核心功能是进行血浆超滤以产生原尿。肾小球滤过屏障由有窗孔的内皮细胞、肾小球基底膜和足细胞组成,足细胞是一种间充质样细胞,具有富含肌动蛋白丝的突起,即“足突”。它们的结构和功能由肌动蛋白和几种肌动蛋白结合蛋白维持和调节,这些蛋白的突变可能导致肾小球疾病。由于最初的免疫染色实验已证明肾小球中有强烈的脑 drebrin 反应,因此对该蛋白在多种哺乳动物肾脏中的分布进行了详细研究。双标记共聚焦激光扫描显微镜显示,在人、牛、小鼠和大鼠肾脏的系膜细胞中脑 drebrin 富集。在 Thy-1.1 肾炎大鼠肾小球中,该蛋白集中在系膜细胞突起中,并在其形成和重塑过程中上调。在成年人类和牛的肾脏中,免疫电子显微镜证实脑 drebrin 还积聚在足细胞的足突中。相比之下,啮齿动物肾小球的足细胞仅在发育早期含有大量的脑 drebrin。然而,在诱导形成细胞突起的培养小鼠足细胞中,脑 drebrin 集中在这些突起中,部分与其他肌动蛋白结合蛋白共定位。人和牛肾脏的蛋白质提取物包含脑 drebrin 和肌动蛋白的 20 S 复合物,即所谓的 drebrosomes。总之,脑 drebrin 必须添加到调节系膜细胞突起和足细胞足突肌动蛋白动力学的肌动蛋白结合蛋白列表中。确定其在遗传性和获得性肾小球病中的作用将很重要。