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本文引用的文献

1
UT-B1 mediates transepithelial urea flux in the rat gastrointestinal tract.UT-B1 介导大鼠胃肠道内的跨上皮尿素通量。
J Membr Biol. 2011 Feb;239(3):123-30. doi: 10.1007/s00232-010-9331-9. Epub 2010 Dec 3.
2
Protein kinase C regulates urea permeability in the rat inner medullary collecting duct.蛋白激酶 C 调控大鼠内髓集合管的尿素通透性。
Am J Physiol Renal Physiol. 2010 Dec;299(6):F1401-6. doi: 10.1152/ajprenal.00322.2010. Epub 2010 Sep 22.
3
Internalization of UT-A1 urea transporter is dynamin dependent and mediated by both caveolae- and clathrin-coated pit pathways.UT-A1 尿素转运体的内化是网格蛋白小窝和 caveolae 途径介导的,依赖于动力蛋白。
Am J Physiol Renal Physiol. 2010 Dec;299(6):F1389-95. doi: 10.1152/ajprenal.00718.2009. Epub 2010 Sep 22.
4
Genetic variants of human urea transporter-2 are associated with metabolic syndrome in Asian population.人类尿素转运蛋白-2 的遗传变异与亚洲人群的代谢综合征有关。
Clin Chim Acta. 2010 Dec 14;411(23-24):2009-13. doi: 10.1016/j.cca.2010.08.025. Epub 2010 Aug 23.
5
Vasopressin increases phosphorylation of Ser84 and Ser486 in Slc14a2 collecting duct urea transporters.血管加压素增加 Slc14a2 集合管尿素转运蛋白 Ser84 和 Ser486 的磷酸化。
Am J Physiol Renal Physiol. 2010 Sep;299(3):F559-67. doi: 10.1152/ajprenal.00617.2009. Epub 2010 Jun 24.
6
The N-terminal 81-aa fragment is critical for UT-A1 urea transporter bioactivity.N 端 81 个氨基酸的片段对 UT-A1 尿素转运体的生物活性至关重要。
J Epithel Biol Pharmacol. 2010;3:34-39. doi: 10.2174/1875044301003010034.
7
Functional characterization of the central hydrophilic linker region of the urea transporter UT-A1: cAMP activation and snapin binding.尿素转运蛋白 UT-A1 中心亲水连接区的功能特征:cAMP 激活和衔接蛋白结合。
Am J Physiol Cell Physiol. 2010 Jun;298(6):C1431-7. doi: 10.1152/ajpcell.00497.2009. Epub 2010 Mar 24.
8
Jk(a-b-) phenotype screening by the urea lysis test in Thai blood donors.在泰国献血者中通过尿素溶解试验进行 Jk(a-b-) 表型筛查。
Blood Transfus. 2010 Jan;8(1):17-20. doi: 10.2450/2009.0104-09.
9
Phosphorylation of UT-A1 on serine 486 correlates with membrane accumulation and urea transport activity in both rat IMCDs and cultured cells.UT-A1 丝氨酸 486 的磷酸化与大鼠 IMCD 和培养细胞中的膜积累和尿素转运活性相关。
Am J Physiol Renal Physiol. 2010 Apr;298(4):F935-40. doi: 10.1152/ajprenal.00682.2009. Epub 2010 Jan 13.
10
Expression of transporters involved in urine concentration recovers differently after cessation of lithium treatment.表达转运体参与尿液浓缩的恢复在锂治疗停止后不同。
Am J Physiol Renal Physiol. 2010 Mar;298(3):F601-8. doi: 10.1152/ajprenal.00424.2009. Epub 2009 Dec 23.

SLC14A 家族尿素转运体的新兴生理作用。

The emerging physiological roles of the SLC14A family of urea transporters.

机构信息

School of Biology & Environmental Science, College of Life Sciences, University College Dublin, Belfield, Dublin, Ireland.

出版信息

Br J Pharmacol. 2011 Dec;164(7):1780-92. doi: 10.1111/j.1476-5381.2011.01377.x.

DOI:10.1111/j.1476-5381.2011.01377.x
PMID:21449978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3246703/
Abstract

In mammals, urea is the main nitrogenous breakdown product of protein catabolism and is produced in the liver. In certain tissues, the movement of urea across cell membranes is specifically mediated by a group of proteins known as the SLC14A family of facilitative urea transporters. These proteins are derived from two distinct genes, UT-A (SLC14A2) and UT-B (SLC14A1). Facilitative urea transporters play an important role in two major physiological processes - urinary concentration and urea nitrogen salvaging. Although UT-A and UT-B transporters both have a similar basic structure and mediate the transport of urea in a facilitative manner, there are a number of significant differences between them. UT-A transporters are mainly found in the kidney, are highly specific for urea, have relatively lower transport rates and are highly regulated at both gene expression and cellular localization levels. In contrast, UT-B transporters are more widespread in their tissue location, transport both urea and water, have a relatively high transport rate, are inhibited by mercurial compounds and currently appear to be less acutely regulated. This review details the fundamental research that has so far been performed to investigate the function and physiological significance of these two types of urea transporters.

摘要

在哺乳动物中,尿素是蛋白质分解代谢的主要含氮产物,由肝脏产生。在某些组织中,尿素穿过细胞膜的运动是由一组被称为 SLC14A 家族的易化尿素转运蛋白特异性介导的。这些蛋白来源于两个不同的基因,UT-A(SLC14A2)和 UT-B(SLC14A1)。易化尿素转运蛋白在两个主要的生理过程中发挥重要作用——尿液浓缩和尿素氮回收。虽然 UT-A 和 UT-B 转运蛋白具有相似的基本结构,并且以易化的方式介导尿素的转运,但它们之间存在许多显著的差异。UT-A 转运蛋白主要存在于肾脏中,对尿素具有高度特异性,转运速率相对较低,并且在基因表达和细胞定位水平都受到高度调节。相比之下,UT-B 转运蛋白在组织中的分布更为广泛,既能转运尿素又能转运水,转运速率相对较高,受汞化合物抑制,目前似乎受到的调节不太敏感。本综述详细介绍了迄今为止为研究这两种类型的尿素转运蛋白的功能和生理意义而进行的基础研究。