Tissue Distribution, Expression and Regulation of Urea Transporters.

Q1 Biochemistry, Genetics and Molecular Biology
Nannan Li, Janet D Klein, Jeff M Sands, Baoxue Yang
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引用次数: 0

Abstract

UT-A and UT-B families of urea transporters consist of multiple isoforms with the majority of the isoforms located in the kidney. UT-B (Slc14A1) in kidney is primarily located in the descending vasa recta. The UT-A (Slc14A2) urea transporter family comprises six distinct isoforms, three of which are predominantly found in the kidney. Specifically, UT-A1 and UT-A3 are located in the inner medullary collecting duct (IMCD), while UT-A2 is situated in the thin descending limb. These transporters play a crucial role in the renal concentration of urine. The regulation of renal urea transporter activity involves acute modifications through phosphorylation and subsequent translocation to the plasma membrane. In response to stimulation by vasopressin or hypertonicity, UT-A1 and UT-A3 accumulate in the IMCD plasma membrane. Chronic regulation of IMCD urea transporters involves hormonal modulation of protein expression levels, such as adrenal steroids, low-protein diets, electrolyte abnormalities, aging or other pathologic conditions. This chapter provides a brief overview of the tissue distribution, expression of the urea transporter isoforms, locations in the kidney, and regulation of urea transporters.

尿素转运蛋白的组织分布、表达和调控。
尿素转运蛋白UT-A和UT-B家族由多种异构体组成,其中大多数异构体位于肾脏。UT-B (Slc14A1)在肾脏中主要位于直降血管。UT-A (Slc14A2)尿素转运蛋白家族包括六种不同的亚型,其中三种主要存在于肾脏中。具体来说,UT-A1和UT-A3位于髓内集管(IMCD),而UT-A2位于薄降支。这些转运蛋白在肾脏尿液浓度中起着至关重要的作用。肾尿素转运蛋白活性的调节涉及通过磷酸化和随后的转运到质膜的急性修饰。在抗利尿激素或高渗性刺激下,UT-A1和UT-A3在IMCD质膜中积累。IMCD尿素转运体的慢性调节涉及蛋白质表达水平的激素调节,如肾上腺类固醇、低蛋白饮食、电解质异常、衰老或其他病理条件。本章简要介绍了组织分布、尿素转运蛋白异构体的表达、肾脏中的位置以及尿素转运蛋白的调控。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sub-cellular biochemistry
Sub-cellular biochemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
5.90
自引率
0.00%
发文量
33
期刊介绍: The book series SUBCELLULAR BIOCHEMISTRY is a renowned and well recognized forum for disseminating advances of emerging topics in Cell Biology and related subjects. All volumes are edited by established scientists and the individual chapters are written by experts on the relevant topic. The individual chapters of each volume are fully citable and indexed in Medline/Pubmed to ensure maximum visibility of the work.
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