Impact of Ring Finger Protein 20 and Its Downstream Regulation on Renal Tubular Injury in a Unilateral Nephrectomy Mouse Model Fed a High-Fat Diet

Nutrients. 2023 Nov 29;15(23):4959. doi: 10.3390/nu15234959.

Abstract

Abnormal lipid metabolism increases the relative risk of kidney disease in patients with a single kidney. Using transcriptome analysis, we investigated whether a high-fat diet leads to abnormalities in lipid metabolism and induces kidney cell-specific damage in unilateral nephrectomy mice. Mice with unilateral nephrectomy fed a high-fat diet for 12 weeks exhibited progressive renal dysfunction in proximal tubules, including lipid accumulation, vacuolization, and cell damage. Ring finger protein 20 (RNF20) is a ligase of nuclear receptor corepressor of peroxisome proliferator-activated receptors (PPARs). The transcriptome analysis revealed the involvement of RNF20-related transcriptome changes in PPAR signaling, lipid metabolism, and water transmembrane transporter under a high-fat diet and unilateral nephrectomy. In vitro treatment of proximal tubular cells with palmitic acid induced lipotoxicity by altering RNF20, PPARα, and ATP-binding cassette subfamily A member 1 (ABCA1) expression. PPARγ and aquaporin 2 (AQP2) expression decreased in collecting duct cells, regulating genetic changes in the water reabsorption process. In conclusion, a high-fat diet induces lipid accumulation under unilateral nephrectomy via altering RNF20-mediated regulation and causing functional damage to cells as a result of abnormal lipid metabolism, thereby leading to structural and functional kidney deterioration.

Keywords: kidney damage; lipid metabolism; peroxisome proliferator-activated receptor signaling; ring finger protein 20.

MeSH terms

  • Animals
  • Aquaporin 2 / metabolism
  • Diet, High-Fat* / adverse effects
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Diseases* / metabolism
  • Lipid Metabolism / physiology
  • Lipids
  • Mice
  • Nephrectomy / adverse effects
  • PPAR alpha / metabolism
  • Ubiquitin-Protein Ligases* / genetics
  • Ubiquitin-Protein Ligases* / metabolism
  • Water / metabolism

Substances

  • Aquaporin 2
  • Lipids
  • PPAR alpha
  • RNF20 protein, mouse
  • Ubiquitin-Protein Ligases
  • Water