Kim J, Tisher C C, Linser P J, Madsen K M
Division of Nephrology, Hypertension and Transplantation, University of Florida, Gainesville 32610.
J Am Soc Nephrol. 1990 Sep;1(3):245-56. doi: 10.1681/ASN.V13245.
At least two configurations of intercalated cells, type A and type B, are present in the cortical collecting duct. Intercalated cells are rich in carbonic anhydrase. However, it is not known whether there are differences in the level and subcellular distribution of this enzyme between type A and type B intercalated cells. The purpose of this study was to determine the relative content and intracellular distribution of carbonic anhydrase II in the various subpopulations of intercalated cells in the rat collecting duct. A rabbit polyclonal antibody directed against mouse erythrocyte carbonic anhydrase II was employed to localize carbonic anhydrase, II by light and electron microscopy by an indirect immunoperoxidase method. A Western immunoblot analysis of homogenates of rat kidney cortex and medulla with the carbonic anhydrase II antibody revealed a single polypeptide band at 29 kDa corresponding to the molecular size of carbonic anhydrase II. By both light and electron microscopy, carbonic anhydrase II immunoreactivity was present in all intercalated cells but the intensity of staining was much greater in type A than in type B cells. In addition, immunostaining in type A cells was especially pronounced in the apical cytoplasm and apical microprojections whereas in type B cells, immunostaining was more diffuse throughout the cytoplasm. A third configuration of intercalated cell with diffuse immunostaining for carbonic anhydrase II was occasionally observed in the connecting segment. Very weak immunostaining was present in principal cells, whereas connecting tubule cells and inner medullary collecting duct cells were negative for carbonic anhydrase II.(ABSTRACT TRUNCATED AT 250 WORDS)
皮质集合管中存在至少两种类型的闰细胞,即A型和B型。闰细胞富含碳酸酐酶。然而,尚不清楚A型和B型闰细胞中该酶的水平和亚细胞分布是否存在差异。本研究的目的是确定大鼠集合管中闰细胞各亚群中碳酸酐酶II的相对含量和细胞内分布。使用针对小鼠红细胞碳酸酐酶II的兔多克隆抗体,通过间接免疫过氧化物酶法,在光镜和电镜下定位碳酸酐酶II。用碳酸酐酶II抗体对大鼠肾皮质和髓质匀浆进行Western免疫印迹分析,结果显示在29 kDa处有一条单一的多肽条带,对应于碳酸酐酶II的分子大小。光镜和电镜观察均显示,所有闰细胞中均存在碳酸酐酶II免疫反应性,但A型细胞的染色强度远高于B型细胞。此外,A型细胞的免疫染色在顶端细胞质和顶端微突起中尤为明显,而在B型细胞中,免疫染色在整个细胞质中更为弥散。在连接段偶尔可观察到第三种类型的闰细胞,其对碳酸酐酶II呈弥散性免疫染色。主细胞中存在非常微弱的免疫染色,而连接小管细胞和内髓集合管细胞对碳酸酐酶II呈阴性。(摘要截取自250字)