The urea transporter UT-A1 plays a predominant role in a urea-dependent urine-concentrating mechanism

被引:13
作者
Geng, Xiaoqiang [1 ]
Zhang, Shun [1 ]
He, Jinzhao [1 ]
Ma, Ang [1 ]
Li, Yingjie [1 ]
Li, Min [1 ]
Zhou, Hong [1 ]
Chen, Guangping [2 ]
Yang, Baoxue [1 ,3 ]
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Pharmacol, State Key Lab Nat & Biomimet Drugs, Beijing, Peoples R China
[2] Emory Univ, Sch Med, Dept Physiol, Atlanta, GA 30322 USA
[3] Minist Educ, Key Lab Mol Cardiovasc Sci, Beijing, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金; 北京市自然科学基金;
关键词
animal model; CRISPR; Cas9; gene knockout; kidney; renal physiology; UT-A1; urea transporter; diuresis; electrolyte metabolism; UT-A; MICE LACKING; MEMBRANE ACCUMULATION; WATER CHANNEL; MESSENGER-RNA; CLONING; LOCALIZATION; KNOCKOUT; GENE; PHOSPHORYLATION;
D O I
10.1074/jbc.RA120.013628
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Urea transporters are a family of urea-selective channel proteins expressed in multiple tissues that play an important role in the urine-concentrating mechanism of the mammalian kidney. Previous studies have shown that knockout of urea transporter (UT)-B, UT-A1/A3, or all UTs leads to urea-selective diuresis, indicating that urea transporters have important roles in urine concentration. Here, we sought to determine the role of UT-A1 in the urine-concentrating mechanism in a newly developed UT-A1?knockout mouse model. Phenotypically, daily urine output in UT-A1?knockout mice was nearly 3-fold that of WT mice and 82% of all-UT?knockout mice, and the UT-A1?knockout mice had significantly lower urine osmolality than WT mice. After 24-h water restriction, acute urea loading, or high-protein (40%) intake, UT-A1?knockout mice were unable to increase urine-concentrating ability. Compared with all-UT?knockout mice, the UT-A1?knockout mice exhibited similarly elevated daily urine output and decreased urine osmolality, indicating impaired urea-selective urine concentration. Our experimental findings reveal that UT-A1 has a predominant role in urea-dependent urine-concentrating mechanisms, suggesting that UT-A1 represents a promising diuretic target.
引用
收藏
页码:9893 / 9900
页数:8
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