| Literature DB >> 32461256 |
Xiaoqiang Geng1, Shun Zhang1, Jinzhao He1, Ang Ma1, Yingjie Li1, Min Li1, Hong Zhou1, Guangping Chen2, Baoxue Yang3,4.
Abstract
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.Entities:
Keywords: CRISPR/Cas9; UT-A1; animal model; diuresis; electrolyte metabolism; gene knockout; kidney; renal physiology; urea transporter
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Year: 2020 PMID: 32461256 PMCID: PMC7380188 DOI: 10.1074/jbc.RA120.013628
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157