Transcriptome analysis of a rat PKD model: Importance of genes involved in extracellular matrix metabolism

• DOI: 10.1038/sj.ki.5000309
• Publication Date: 2006-03-15T17:14:55Z
• Authors: M. Riera; S. Burtey; M. Fontés
• Keywords: Polycystic Kidney Diseases; 0303 health sciences; polycystic kidney disease; Transcription, Genetic; extracellular matrix; Gene Expression Profiling; fibrosis; Gene Expression; Han:SPRD rats; Rats, Mutant Strains; Extracellular Matrix; Rats; Rats, Sprague-Dawley; Disease Models, Animal; 03 medical and health sciences; Gene Expression Regulation; fibronectin; Nephrology; Animals; Female; microarrays; Oligonucleotide Array Sequence Analysis

Transcriptome analysis of a rat polycystic kidney disease (PKD) model: importance of genes involved in extracellular matrix metabolism. PKD is a common genetic cause of chronic renal failure, and is characterized by the accumulation of fluid-filled cysts in the kidneys and other organs. Abnormalities in the expression of selected genes thought to be involved in cystogenesis have been described, but no systematic analysis of the global transcriptomal pattern has been reported. With this aim, a rat oligomicroarray was used to identify variations in gene expression in Han:Sprague-Dawley Cy/Cy rats, an animal model presenting a severe PKD phenotype. Some upregulated genes were validated using real-time polymerase chain reaction in Cy/Cy and Cy/+ rats. Among the 350 genes identified as being upregulated, we found about 30 genes involved in extracellular matrix metabolism. These genes encoded proteins or peptides that could be implicated into two different biological processes: molecules involved in fibrosis and proteins involved in adhesion to the extracellular matrix. In heterozygotes, some genes (glypican 3, fibronectin 1) were already upregulated in early stages of the disease. We conclude that differential regulation of genes linked to extracellular matrix metabolism may be one of the first events leading to tubule enlargement and subsequent cyst formation in PKD.