Albumin downregulates Klotho in tubular cells

Nephrol Dial Transplant. 2018 Oct 1;33(10):1712-1722. doi: 10.1093/ndt/gfx376.

Abstract

Background: Kidney tubular cells are the main sources of Klotho, a protein with phosphaturic action. Genetic Klotho deficiency causes premature cardiovascular aging in mice. Human chronic kidney disease (CKD) is characterized by acquired Klotho deficiency. Despite the lack of uremic toxin accumulation, Category G1 CKD [(normal glomerular filtration rate (GFR)] is already associated with decreased Klotho and with premature cardiovascular aging.

Methods: We have explored whether albuminuria, a criterion to diagnose CKD when GFR is normal, may directly decrease Klotho expression in human CKD, preclinical models and cultured tubular cells.

Results: In a CKD cohort, albuminuria correlated with serum phosphate after adjustment for GFR, age and sex. In this regard, urinary Klotho was decreased in patients with pathological albuminuria but preserved GFR. Proteinuria induced in rats by puromycin aminonucleoside and in mice by albumin overload was associated with interstitial inflammation and reduced total kidney Klotho messenger ribonucleic acid (mRNA) expression. Western blot disclosed reduced kidney Klotho protein in proteinuric rats and mice and immunohistochemistry localized the reduced kidney Klotho expression to tubular cells in proteinuric animals. In cultured murine and human tubular cells, albumin directly decreased Klotho mRNA and protein expression. This was inhibited by trichostatin A, an inhibitor of histone deacetylases, but unlike cytokine-induced Klotho downregulation, not by inhibitors of nuclear factor kappa-light-chain-enhancer of activated B cells.

Conclusions: In conclusion, albumin directly decreases Klotho expression in cultured tubular cells. This may explain, or at least contribute to, the decrease in Klotho and promote fibroblast growth factor 23 resistance in early CKD categories, as observed in preclinical and clinical proteinuric kidney disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Albumins / pharmacology*
  • Albuminuria / etiology
  • Albuminuria / metabolism*
  • Albuminuria / pathology
  • Animals
  • Cells, Cultured
  • Cohort Studies
  • Cytokines / metabolism
  • Disease Models, Animal
  • Down-Regulation
  • Female
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism
  • Gene Expression Regulation / drug effects*
  • Glomerular Filtration Rate
  • Glucuronidase / genetics
  • Glucuronidase / metabolism*
  • Humans
  • Inflammation / etiology
  • Inflammation / metabolism*
  • Inflammation / pathology
  • Kidney Tubules / drug effects
  • Kidney Tubules / metabolism*
  • Kidney Tubules / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Proteinuria / etiology
  • Proteinuria / metabolism
  • Proteinuria / pathology
  • Rats
  • Rats, Wistar
  • Renal Insufficiency, Chronic / complications
  • Renal Insufficiency, Chronic / physiopathology*

Substances

  • Albumins
  • Cytokines
  • Fibroblast Growth Factors
  • fibroblast growth factor 23
  • Glucuronidase
  • klotho protein