Hyperlipidemia-Associated Renal Damage Decreases Klotho Expression in Kidneys from ApoE Knockout Mice

• DOI: 10.1371/journal.pone.0083713
• Publication Date: 2013-12-30T21:26:01Z
• Authors: Cristina Sastre; Alfonso Rubio-Nav...; Irene Buendía; Carmen Gómez-Guer...; Julia Blanco; Sebastian Mas; Jesús Egido; Luis Miguel Blanc...; Alberto Ortiz; Juan Antonio Moreno
• Keywords: Male; 0301 basic medicine; Medicina; Science; Gene Expression; Hyperlipidemias; Epithelial cells; Kidney; Cell Line; Mice; 03 medical and health sciences; Apolipoproteins E; Animals; Klotho Proteins; Cells, Cultured; Glucuronidase; Inflammation; Mice, Knockout; Q; R; Kidneys; Lipid Metabolism; Diet; Lipoproteins, LDL; Disease Models, Animal; Cholesterol; Hyperlipidemia; Gene Expression Regulation; Oxidative stress; Medicine; Protein expression; Cytokines; Kidney Diseases; Inflammation Mediators; Research Article

Klotho is a renal protein with anti-aging properties that is downregulated in conditions related to kidney injury. Hyperlipidemia accelerates the progression of renal damage, but the mechanisms of the deleterious effects of hyperlipidemia remain unclear.We evaluated whether hyperlipidemia modulates Klotho expression in kidneys from C57BL/6 and hyperlipidemic apolipoprotein E knockout (ApoE KO) mice fed with a normal chow diet (ND) or a Western-type high cholesterol-fat diet (HC) for 5 to 10 weeks, respectively.In ApoE KO mice, the HC diet increased serum and renal cholesterol levels, kidney injury severity, kidney macrophage infiltration and inflammatory chemokine expression. A significant reduction in Klotho mRNA and protein expression was observed in kidneys from hypercholesteromic ApoE KO mice fed a HC diet as compared with controls, both at 5 and 10 weeks. In order to study the mechanism involved in Klotho down-regulation, murine tubular epithelial cells were treated with ox-LDL. Oxidized-LDL were effectively uptaken by tubular cells and decreased both Klotho mRNA and protein expression in a time- and dose-dependent manner in these cells. Finally, NF-κB and ERK inhibitors prevented ox-LDL-induced Klotho downregulation.Our results suggest that hyperlipidemia-associated kidney injury decreases renal expression of Klotho. Therefore, Klotho could be a key element explaining the relationship between hyperlipidemia and aging with renal disease.