Literature DB >> 24674586

Case study: polycystic livers in a transgenic mouse line.

Jamie Lovaglio1, James E Artwohl2, Christopher J Ward3, Thomas Gh Diekwisch4, Yoshihiro Ito4, Jeffrey D Fortman1.   

Abstract

Three mice (2 male, 1 female; age, 5 to 16 mo) from a mouse line transgenic for keratin 14 (K14)-driven LacZ expression and on an outbred Crl:CD1(ICR) background, were identified as having distended abdomens and livers that were diffusely enlarged by numerous cysts (diameter, 0.1 to 2.0 cm). Histopathology revealed hepatic cysts lined by biliary type epithelium and mild chronic inflammation, and confirmed the absence of parasites. Among 21 related mice, 5 additional affected mice were identified via laparotomy. Breeding of these 5 mice (after 5 mo of age) did not result in any offspring; the K14 mice with polycystic livers failed to reproduce. Affected male mice had degenerative testicular lesions, and their sperm was immotile. Nonpolycystic K14 control male mice bred well, had no testicular lesions, and had appropriate sperm motility. Genetic analysis did not identify an association of this phenotype with the transgene or insertion site.

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Year:  2014        PMID: 24674586      PMCID: PMC3997289     

Source DB:  PubMed          Journal:  Comp Med        ISSN: 1532-0820            Impact factor:   0.982


  34 in total

1.  Polycystic liver disease: new insights into disease pathogenesis.

Authors:  Tatyana Masyuk; Nicholas LaRusso
Journal:  Hepatology       Date:  2006-05       Impact factor: 17.425

Review 2.  Polycystic kidney disease: genes, proteins, animal models, disease mechanisms and therapeutic opportunities.

Authors:  V E Torres; P C Harris
Journal:  J Intern Med       Date:  2007-01       Impact factor: 8.989

3.  Long-distance genome walking using the long and accurate polymerase chain reaction.

Authors:  G S Min; J R Powell
Journal:  Biotechniques       Date:  1998-03       Impact factor: 1.993

4.  Paternal age and its effects on reproduction in C57BL/6NNia mice.

Authors:  T A Parkening; T J Collins; W W Au
Journal:  J Gerontol       Date:  1988-05

5.  Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesion.

Authors:  B K Yoder; W G Richards; C Sommardahl; W E Sweeney; E J Michaud; J E Wilkinson; E D Avner; R P Woychik
Journal:  Am J Pathol       Date:  1997-06       Impact factor: 4.307

6.  A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD).

Authors:  Markus Moser; Sonja Matthiesen; Jutta Kirfel; Hubert Schorle; Carsten Bergmann; Jan Senderek; Sabine Rudnik-Schöneborn; Klaus Zerres; Reinhard Buettner
Journal:  Hepatology       Date:  2005-05       Impact factor: 17.425

Review 7.  Polycystic disease of the liver.

Authors:  Gregory T Everson; Matthew R G Taylor; R Brian Doctor
Journal:  Hepatology       Date:  2004-10       Impact factor: 17.425

8.  Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.

Authors:  J H Moyer; M J Lee-Tischler; H Y Kwon; J J Schrick; E D Avner; W E Sweeney; V L Godfrey; N L Cacheiro; J E Wilkinson; R P Woychik
Journal:  Science       Date:  1994-05-27       Impact factor: 47.728

Review 9.  Intraflagellar transport and cilia-dependent renal disease: the ciliary hypothesis of polycystic kidney disease.

Authors:  Gregory J Pazour
Journal:  J Am Soc Nephrol       Date:  2004-10       Impact factor: 10.121

10.  Adult polycystic liver and kidney diseases are separate entities.

Authors:  P J Karhunen; M Tenhu
Journal:  Clin Genet       Date:  1986-07       Impact factor: 4.438

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