NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE19058 Query DataSets for GSE19058
Status Public on Jan 25, 2011
Title Identification of cathepsin L as a potential sex-specific biomarker for renal damage
Organism Rattus norvegicus
Experiment type Expression profiling by array
Summary The renin-angiotensin system is a well-known regulator of blood pressure and plays an important role in the pathogenesis of cardiovascular disease and renal damage. Genetic factors, including single nucleotide polymorphisms and sex, are increasingly recognized as potential risk factors for the development of cardiovascular disease. Double transgenic rats (dTGR), harboring human renin and angiotensinogen genes, were used in this study to investigate potential sex differences influencing renal function and renal gene expression. dTGR males and females had comparable increases in blood pressure, whereas body weight, albuminuria/proteinuria and urine flow rate were higher in males. At eight weeks of age renal plasma flow and glomerular filtration rate were proportionally lower in males, and renal vascular resistance tended to be higher. Males developed more severe tubulointerstitial and vascular lesions. By the end of week eight, 40% of the males, but none of the females had died. Genome expression studies were performed with RNA from kidneys of 7-week-old male and female dTGR and control rats to further investigate the sex-related differences on a molecular level. Forty-five genes showed sex-dependent expression patterns in dTGR that were significantly different compared to controls. Cathepsin L, one of the genes differentially expressed between the sexes, was shown to be also strongly associated with the degree of renal injury. In dTGR, urinary CTSL at week 7 was higher in males (ng/24 hours: M 512 +/- 163, F 132 +/- 70). These results reveal a potential new biomarker for the personalized diagnosis and management of chronic kidney disease.
 
Overall design Four condition experiment, dTGR male vs Control male and dTGR female vs Control female. Biological replicates: 8 rats per condition
 
Contributor(s) Bauer Y, Hess P, Qiu C, Klenk A, Renault B, Wanner D, Studer R, Killer N, Stalder AK, Stritt M, Strasser DS, Farine H, Kauser K, Clozel M, Fischli W, Nayler O
Citation(s) 21357272
Submission date Nov 17, 2009
Last update date Dec 21, 2016
Contact name Axel Klenk
E-mail(s) axel.klenk@idorsia.com
Organization name Idorsia Pharmaceuticals Ltd.
Department Research Informatics
Street address Hegenheimermattweg 91
City Allschwil
ZIP/Postal code 4123
Country Switzerland
 
Platforms (1)
GPL4135 Agilent-014879 Whole Rat Genome Microarray 4x44K G4131F (Feature Number version)
Samples (31)
GSM471612 kidney_double-transgenic_rat_female_rep1
GSM471613 kidney_double-transgenic_rat_female_rep2
GSM471614 kidney_double-transgenic_rat_female_rep3
Relations
BioProject PRJNA120561

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE19058_RAW.tar 481.4 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap