UT-A1/A3 knockout mice show reduced fibrosis following unilateral ureteral obstruction.
Fitra RiantoAkihiro KumaCarla L EllisFaten HassounahEva L RodriguezXiaonan H WangJeff M SandsJanet D KleinPublished in: American journal of physiology. Renal physiology (2020)
Renal fibrosis is a major contributor to the development and progression of chronic kidney disease. A low-protein diet can reduce the progression of chronic kidney disease and reduce the development of renal fibrosis, although the mechanism is not well understood. Urea reabsorption into the inner medulla is regulated by inner medullary urea transporter (UT)-A1 and UT-A3. Inhibition or knockout of UT-A1/A3 will reduce interstitial urea accumulation, which may be beneficial in reducing renal fibrosis. To test this hypothesis, the effect of unilateral ureteral obstruction (UUO) was compared in wild-type (WT) and UT-A1/A3 knockout mice. UUO causes increased extracellular matrix associated with increases in transforming growth factor-β, vimentin, and α-smooth muscle actin (α-SMA). In WT mice, UUO increased the abundance of three markers of fibrosis: transforming growth factor-β, vimentin, and α-SMA. In contrast, in UT-A1/A3 knockout mice, the increase following UUO was significantly reduced. Consistent with the Western blot results, immunohistochemical staining showed that the levels of vimentin and α-SMA were increased in WT mice with UUO and that the increase was reduced in UT-A1/A3 knockout mice with UUO. Masson's trichrome staining showed increased collagen in WT mice with UUO, which was reduced in UT-A1/A3 knockout mice with UUO. We conclude that reduced UT activity reduces the severity of renal fibrosis following UUO.
Keyphrases
- transforming growth factor
- wild type
- chronic kidney disease
- epithelial mesenchymal transition
- extracellular matrix
- smooth muscle
- end stage renal disease
- liver fibrosis
- magnetic resonance imaging
- computed tomography
- small molecule
- physical activity
- metabolic syndrome
- microbial community
- skeletal muscle
- cell migration
- amino acid
- tissue engineering