Role of Klotho in Osteoporosis and Renal Osteodystrophy

Abstract

The most significant findings from the last period are the following. 1) We are the first to show that Klotho is expressed in proximal tubules and that in vivo deletion of Klotho from proximal tubules leads to reduced urinary phosphate wasting (AIM 2). Three mouse models were established to confirm our findings. It seems, however, that there is an interrelationship between proximal and distal tubules since deletion of Klotho from either target tissue leads only to a mild phenotype, so compensatory mechanisms are suggested. 2) In AIM3 we found that Klotho expression in bone forming cells is required to induce FGF23 transcription upon renal failure. Such findings can ultimately lead to therapeutic interventions to block the increase in FGF23 production during renal failure. Here two mouse models resulted in similar results, so we are very confident about our results.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2015
Accession Number
AD1005934

Entities

People

  • Beate Lanske

Organizations

  • Harvard University

Tags

DTIC Thesaurus Topics

  • Bone Diseases
  • Cells
  • Department Of Defense
  • Diseases And Disorders
  • Genes
  • Genetics
  • Health Services
  • Kidney Diseases
  • Osteoblasts
  • Osteogenesis
  • Osteoporosis
  • Spine
  • Surgery

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