Overexpression of klotho protein modulates uninephrectomy-induced compensatory renal hypertrophy by suppressing IGF-I signals

Biochem Biophys Res Commun. 2011 Apr 1;407(1):39-43. doi: 10.1016/j.bbrc.2011.02.089. Epub 2011 Feb 24.

Abstract

The klotho gene is highly expressed in the distal convoluted tubule of the kidney, while its encoded protein has many physiological and pathophysiological renal roles. We investigated the effect of klotho protein on physiological compensatory renal hypertrophy after nephrectomy in klotho transgenic (KLTG) mice. Renal hypertrophy was suppressed in KLTG mice compared with wild-type mice, and this was associated with suppression of insulin growth factor-1 (IGF-1) signaling by klotho protein. In vitro, IGF-1 signaling was suppressed in human proximal tubular cells transfected with the klotho plasmid. Our data suggest that klotho modulates compensatory renal hypertrophy after nephrectomy via suppression of the IGF-1 signaling pathway, indicating a novel physiological role for klotho protein in the kidney.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Glucuronidase / genetics
  • Glucuronidase / physiology*
  • Humans
  • Hypertrophy / genetics
  • Hypertrophy / pathology
  • Insulin-Like Growth Factor I / antagonists & inhibitors*
  • Insulin-Like Growth Factor I / metabolism
  • Kidney / pathology*
  • Kidney / physiopathology
  • Kidney Glomerulus / pathology
  • Kidney Glomerulus / physiopathology
  • Kidney Tubules, Proximal / metabolism
  • Kidney Tubules, Proximal / pathology
  • Klotho Proteins
  • Mice
  • Mice, Transgenic
  • NADPH Oxidases / metabolism
  • Nephrectomy
  • Signal Transduction
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • insulin-like growth factor-1, mouse
  • Insulin-Like Growth Factor I
  • NADPH Oxidases
  • TOR Serine-Threonine Kinases
  • Glucuronidase
  • Klotho Proteins