Increased expression of secreted frizzled-related protein 4 in polycystic kidneys

J Am Soc Nephrol. 2009 Jan;20(1):48-56. doi: 10.1681/ASN.2008040345. Epub 2008 Oct 22.


Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disease associated with progressive renal failure. Although cyst growth and compression of surrounding tissue may account for some loss of renal tissue, the other factors contributing to the progressive renal failure in patients with ADPKD are incompletely understood. Here, we report that secreted frizzled-related protein 4 (sFRP4) is upregulated in human ADPKD and in four different animal models of PKD, suggesting that sFRP4 expression is triggered by a common mechanism that underlies cyst formation. Cyst fluid from ADPKD kidneys activated the sFRP4 promoter and induced production of sFRP4 protein in renal tubular epithelial cell lines. Antagonism of the vasopressin 2 receptor blocked both promoter activity and tubular sFRP4 expression. In addition, sFRP4 selectively influenced members of the canonical Wnt signaling cascade and promoted cystogenesis of the zebrafish pronephros. sFRP4 was detected in the urine of both patients and animals with PKD, suggesting that sFRP4 may be a potential biomarker for monitoring the progression of ADPKD. Taken together, these observations suggest a potential role for SFRP4 in the pathogenesis of ADPKD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cyst Fluid / physiology
  • Disease Models, Animal
  • Humans
  • Kidney / metabolism*
  • Mice
  • Morpholines / pharmacology
  • Nephrons / embryology
  • Polycystic Kidney Diseases / metabolism
  • Polycystic Kidney, Autosomal Dominant / etiology*
  • Polycystic Kidney, Autosomal Dominant / metabolism
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins / physiology*
  • Signal Transduction
  • Spiro Compounds / pharmacology
  • TRPP Cation Channels / physiology
  • Transcription Factors / physiology
  • Wnt Proteins / physiology
  • Xenopus
  • Zebrafish


  • Invs protein, mouse
  • Morpholines
  • Proto-Oncogene Proteins
  • SFRP4 protein, human
  • Spiro Compounds
  • TRPP Cation Channels
  • Transcription Factors
  • Wnt Proteins
  • polycystic kidney disease 2 protein
  • satavaptan