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

Research output: Contribution to journalArticle

39 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)733-741
Number of pages9
JournalPediatric Nephrology
Volume23
Issue number5
DOIs
StatePublished - May 1 2008

Keywords

  • ARPKD
  • Biliary ductal plate malformations
  • Pkhd1
  • Polycystic kidney disease

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Nephrology

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