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Cardiovascular, skeletal, and renal defects in mice with a targeted disruption of the Pkd1 gene

Boulter, Catherine, Mulroy, S., Webb, S., Fleming, S., Brindle, K. and Sandford, R. 2001. Cardiovascular, skeletal, and renal defects in mice with a targeted disruption of the Pkd1 gene. Proceedings of the National Academy of Sciences of the United States of America 98 (21) , pp. 12174-12179. 10.1073/pnas.211191098

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Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by cyst formation in the kidney, liver, and pancreas and is associated often with cardiovascular abnormalities such as hypertension, mitral valve prolapse, and intracranial aneurysms. It is caused by mutations in PKD1 or PKD2, encoding polycystin-1 and -2, which together form a cell surface nonselective cation ion channel. Pkd2−/− mice have cysts in the kidney and pancreas and defects in cardiac septation, whereas Pkd1del34 −/− and Pkd1L −/− mice have cysts but no cardiac abnormalities, although vascular fragility was reported in the latter. Here we describe mice carrying a targeted mutation in Pkd1 (Pkd1del17–21βgeo), which defines its expression pattern by using a lacZ reporter gene and may identify novel functions for polycystin-1. Although Pkd1del17–21βgeo +/− adult mice develop renal and hepatic cysts, Pkd1del17–21βgeo −/− embryos die at embryonic days 13.5–14.5 from a primary cardiovascular defect that includes double outflow right ventricle, disorganized myocardium, and abnormal atrio-ventricular septation. Skeletal development is also severely compromised. These abnormalities correlate with the major sites of Pkd1 expression. During nephrogenesis, Pkd1 is expressed in maturing tubular epithelial cells from embryonic day 15.5. This expression coincides with the onset of cyst formation in Pkd1del34 −/−, Pkd1L −/−, and Pkd2−/− mice, supporting the hypothesis that polycystin-1 and polycystin-2 interact in vivo and that their failure to do so leads to abnormalities in tubule morphology and function.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
Publisher: National Academy of Sciences
ISSN: 0027-8424
Last Modified: 04 Jun 2017 06:39
URI: http://orca-mwe.cf.ac.uk/id/eprint/63276

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