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.
You-Jin KimSe-Hyun OhJeong Hoon LimJang Hee ChoHee-Yeon JungChan Duck KimSun Hee ParkTae-Hwan KwonYong Lim KimPublished in: Nutrients (2023)
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.
Keyphrases
- high fat diet
- insulin resistance
- adipose tissue
- induced apoptosis
- robot assisted
- high fat diet induced
- oxidative stress
- cell cycle arrest
- single cell
- fatty acid
- mouse model
- editorial comment
- poor prognosis
- metabolic syndrome
- skeletal muscle
- multiple sclerosis
- type diabetes
- stem cells
- endoplasmic reticulum stress
- signaling pathway
- cell therapy
- dna damage
- mesenchymal stem cells
- cell death
- gene expression
- protein protein
- mass spectrometry
- transcription factor
- dna methylation
- high glucose
- long non coding rna
- drug induced