Moulin Pierre, Igarashi Takashi, Van der Smissen Patrick, Cosyns Jean-Pierre, Verroust Pierre, Thakker Rajesh V, Scheinman Steven J, Courtoy Pierre J, Devuyst Olivier
Division of Pathology, and Cell Unit, Christian de Duve Institute of Cellular Pathology, Université Catholique de Louvain, Brussels, Belgium.
Kidney Int. 2003 Apr;63(4):1285-95. doi: 10.1046/j.1523-1755.2003.00851.x.
Dent's disease is a proximal tubule (PT) disorder characterized by low-molecular-weight proteinuria (LWMP) that may be associated with hypercalciuria, nephrocalcinosis, and renal failure. It is caused by inactivating mutations of the renal chloride channel ClC-5, which colocalizes with the vacuolar H+-ATPase in PT cells and alpha-type intercalated cells. Examinations of knockout mice have established the role of ClC-5 in PT endocytosis, but the consequences of ClC-5 mutations on the polarity of H+-ATPase and other plasma membrane proteins remain unknown.
We have studied renal biopsies from eight patients with Dent's disease, due to inactivating ClC-5 mutations, by light and electron microscopy, and by immunohistochemical staining. All patients exhibited LMWP, and renal function ranged from normal to end-stage renal failure.
Light microscopy revealed either normal renal architecture or glomerulosclerosis, tubular dedifferentiation and atrophy, and mild interstitial fibrosis. Focal, hyaline casts, sometimes calcified, were identified at all stages. Electron microscopy did not reveal any ultrastructural abnormalities in PT cells, and the endocytic apparatus was apparently normal. However, immunohistochemical studies demonstrated a consistent inversion of H+-ATPase polarity in PT cells to a basolateral distribution contrasting with its apical location in the normal kidney. This inversion of polarity was specific for H+-ATPase and did not affect distribution of aminopeptidase, megalin, and Na+/K+-ATPase. Furthermore, apical H+-ATPase expression was absent in alpha-type intercalated cells.
ClC-5 mutations are associated with modifications in the polarity and expression of H+-ATPase, but not ultrastructural alterations in PT cells. These findings help further understanding of the role of ClC-5 and the pathophysiology of Dent's disease.
邓特氏病是一种近端肾小管(PT)疾病,其特征为低分子量蛋白尿(LWMP),可能伴有高钙尿症、肾钙质沉着症和肾衰竭。它由肾氯通道ClC-5的失活突变引起,该通道与PT细胞和α型闰细胞中的液泡H⁺-ATP酶共定位。对基因敲除小鼠的研究确定了ClC-5在PT内吞作用中的作用,但ClC-5突变对H⁺-ATP酶和其他质膜蛋白极性的影响仍不清楚。
我们通过光学显微镜、电子显微镜和免疫组织化学染色,研究了8例因ClC-5失活突变导致邓特氏病患者的肾活检组织。所有患者均表现出低分子量蛋白尿,肾功能从正常到终末期肾衰竭不等。
光学显微镜检查显示肾结构正常或存在肾小球硬化、肾小管去分化和萎缩以及轻度间质纤维化。在所有阶段均发现局灶性透明管型,有时伴有钙化。电子显微镜检查未发现PT细胞有任何超微结构异常,内吞装置显然正常。然而,免疫组织化学研究表明,PT细胞中H⁺-ATP酶极性持续反转至基底外侧分布,这与正常肾脏中其顶端位置形成对比。这种极性反转是H⁺-ATP酶特有的,不影响氨肽酶、巨膜蛋白和Na⁺/K⁺-ATP酶的分布。此外,α型闰细胞中不存在顶端H⁺-ATP酶表达。
ClC-5突变与H⁺-ATP酶的极性和表达改变有关,但与PT细胞的超微结构改变无关。这些发现有助于进一步理解ClC-5的作用和邓特氏病的病理生理学。