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大鼠肾脏中钠/硫酸根共转运体(NaSi-1)的免疫定位

Immunolocalization of Na/SO4-cotransport (NaSi-1) in rat kidney.

作者信息

Lötscher M, Custer M, Quabius E S, Kaissling B, Murer H, Biber J

机构信息

Institute of Physiology, University Zürich-Irchel, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.

出版信息

Pflugers Arch. 1996 Jul;432(3):373-8. doi: 10.1007/s004240050147.

Abstract

The proximal tubule is the major site for renal reabsorption of sulphate. A sodium-dependent transport system for sulphate (NaSi-1) has recently been identified from a rat kidney cortex cDNA library. Recent work demonstrated that NaSi-1 mRNA is expressed predominantly in proximal tubules. In the present work expression along the nephron of the Na/SO4-cotransporter NaSi-1 was studied by immunofluorescence. A polyclonal antibody was raised in rabbits against a fusion protein containing a 53-amino-acid polypeptide specific for the NaSi-1 sequence. The anti-NaSi-1 polyclonal antibody specifically detected a 68-kDa protein on Western blots and, by immunofluorescence specific staining, was observed in MDCK cells transfected with the NaSi-1 cotransporter. Using rat kidney cortex slices specific NaSi-1-related immunoreactivity was detected in proximal tubules and was restricted to the apical membrane. No immunoreactivity was observed in the other nephron segments. This was confirmed by Western blot analysis using proximal tubular apical and basolateral membranes isolated by free-flow electrophoresis. The results indicate that the Na/SO4-cotransporter NaSi-1 is expressed in the apical membrane of proximal tubular cells and is therefore likely to be involved in proximal reabsorption of sulphate.

摘要

近端小管是肾脏重吸收硫酸盐的主要部位。最近从大鼠肾皮质cDNA文库中鉴定出一种钠依赖性硫酸盐转运系统(NaSi-1)。最近的研究表明,NaSi-1 mRNA主要在近端小管中表达。在本研究中,通过免疫荧光研究了Na/SO4共转运体NaSi-1在肾单位中的表达。用含有对NaSi-1序列特异的53个氨基酸多肽的融合蛋白免疫家兔制备了多克隆抗体。抗NaSi-1多克隆抗体在蛋白质免疫印迹法中特异性检测到一种68 kDa的蛋白质,并且通过免疫荧光特异性染色,在转染了NaSi-1共转运体的MDCK细胞中观察到该抗体。使用大鼠肾皮质切片,在近端小管中检测到特异性的NaSi-1相关免疫反应性,且局限于顶端膜。在其他肾单位节段未观察到免疫反应性。通过使用自由流动电泳分离的近端小管顶端和基底外侧膜进行蛋白质免疫印迹分析证实了这一点。结果表明,Na/SO4共转运体NaSi-1在近端小管细胞的顶端膜中表达,因此可能参与近端硫酸盐的重吸收。

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