Pediatric Nephrology

, Volume 23, Issue 5, pp 733–741

Kidney cysts, pancreatic cysts, and biliary disease in a mouse model of autosomal recessive polycystic kidney disease

  • Scott S. Williams
  • Patricia Cobo-Stark
  • Leighton R. James
  • Stefan Somlo
  • Peter Igarashi
Original Article

DOI: 10.1007/s00467-007-0735-4

Cite this article as:
Williams, S.S., Cobo-Stark, P., James, L.R. et al. Pediatr Nephrol (2008) 23: 733. doi:10.1007/s00467-007-0735-4

Abstract

Mutations in PKHD1 cause autosomal recessive polycystic kidney disease (ARPKD). We produced a mouse model of ARPKD by replacing exons 1–3 of Pkhd1 with a lacZ reporter gene utilizing homologous recombination. This approach yielded heterozygous Pkhd1lacZ/+ mice, that expressed β-galactosidase in tissues where Pkhd1 is normally expressed, and homozygous Pkhd1lacZ/lacZ knockout mice. Heterozygous Pkhd1lacZ/+ mice expressed β-galactosidase in the kidney, liver, and pancreas. Homozygous Pkhd1lacZ/lacZ mice lacked Pkhd1 expression and developed progressive renal cystic disease involving the proximal tubules, collecting ducts, and glomeruli. In the liver, inactivation of Pkhd1 resulted in dilatation of the bile ducts and periportal fibrosis. Dilatation of pancreatic exocrine ducts was uniformly seen in Pkhd1lacZ/lacZ mice, with pancreatic cysts arising less frequently. The expression of β-galactosidase, Pkd1, and Pkd2 was reduced in the kidneys of Pkhd1lacZ/lacZ mice compared with wild-type littermates, but no changes in blood urea nitrogen (BUN) or liver function tests were observed. Collectively, these results indicate that deletion of exons 1–3 leads to loss of Pkhd1 expression and results in kidney cysts, pancreatic cysts, and biliary ductal plate malformations. The Pkhd1lacZ/lacZ mouse represents a new orthologous animal model for studying the pathogenesis of kidney cysts and biliary dysgenesis that characterize human ARPKD.

Keywords

Pkhd1 ARPKD Polycystic kidney disease Biliary ductal plate malformations 

Copyright information

© IPNA 2008

Authors and Affiliations

  • Scott S. Williams
    • 1
  • Patricia Cobo-Stark
    • 2
  • Leighton R. James
    • 2
  • Stefan Somlo
    • 3
  • Peter Igarashi
    • 1
    • 2
  1. 1.Department of PediatricsUniversity of Texas Southwestern Medical CenterDallasUSA
  2. 2.Department of Internal MedicineUniversity of Texas Southwestern Medical CenterDallasUSA
  3. 3.Departments of Internal Medicine and GeneticsYale University School of MedicineNew HavenUSA

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