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首页> 外文期刊>American Journal of Physiology >Ultrastructural localization of Na-K-2Cl cotransporter in thick ascending limb and macula densa of rat kidney.
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Ultrastructural localization of Na-K-2Cl cotransporter in thick ascending limb and macula densa of rat kidney.

机译:Na-K-2Cl协同转运蛋白在大鼠肾脏的粗大上升肢和黄斑部的超微结构定位。

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A bumetanide-sensitive Na-K-2Cl cotransporter, BSC-1, is believed to mediate the apical component of transcellular NaCl absorption in the thick ascending limb (TAL) of Henle's loop. To study its ultrastructural localization in kidney, we used an affinity-purified, peptide-derived polyclonal antibody against rat BSC-1. Immunoblots from rat kidney cortex and outer medulla revealed a solitary 161-kDa band in membrane fractions. Immunocytochemistry of 1-micrometer cryosections demonstrated strong BSC-1 labeling of the apical and subapical regions of medullary and cortical TAL cells. Notably, macula densa cells also exhibited distinct labeling. Distal convoluted tubules and other renal tubule segments were unlabeled. Immunoelectron microscopy demonstrated that BSC-1 labeling was associated with the apical plasma membrane and with subapical intracellular vesicles in medullary and cortical TAL and in macula densa cells. Smooth-surfaced TAL cells, in particular, had extensive BSC-1 labeling of intracellular vesicles. These results support the view that BSC-1 provides the apical pathway for NaCl transport across the TAL and that an extensive intracellular reservoir of BSC-1 is present in a subpopulation of TAL cells. Furthermore, the BSC-1 localization in the apical plasma membrane of macula densa cells is consistent with its proposed role in tubuloglomerular feedback.
机译:据认为,对布美他尼类药物敏感的Na-K-2Cl共转运蛋白BSC-1介导了Henle环的厚上升肢(TAL)中跨细胞NaCl吸收的根尖成分。为了研究其在肾脏中的超微结构定位,我们使用了针对大鼠BSC-1的亲和纯化的,肽源性多克隆抗体。来自大鼠肾皮质和髓质的免疫印迹显示膜级分中有一个单独的161-kDa条带。 1微米冰冻切片的免疫细胞化学分析显示,髓和皮质TAL细胞的根尖和根尖区域具有强烈的BSC-1标记。值得注意的是,黄斑DENSA细胞也表现出独特的标记。远曲小管和其他肾小管段未标记。免疫电子显微镜显示,BSC-1标记与髓质和皮层TAL中以及黄斑部黏膜细胞中的顶质膜和顶下细胞内囊泡有关。特别是表面光滑的TAL细胞具有广泛的BSC-1标记的细胞内囊泡。这些结果支持这样的观点,即BSC-1为NaCl穿过TAL的转运提供了顶端途径,并且在TAL细胞的亚群中存在大量的BSC-1的细胞内储库。此外,BSC-1定位于黄斑部牙髓细胞的顶质膜与其在肾小管肾小球反馈中的拟议作用一致。

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