RGD Reference Report - Targeted disruption of Cd40 in a genetically hypertensive rat model attenuates renal fibrosis and proteinuria, independent of blood pressure. - Rat Genome Database

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Targeted disruption of Cd40 in a genetically hypertensive rat model attenuates renal fibrosis and proteinuria, independent of blood pressure.

Authors: Haller, Steven T  Kumarasamy, Sivarajan  Folt, David A  Wuescher, Leah M  Stepkowski, Stanislaw  Karamchandani, Manish  Waghulde, Harshal  Mell, Blair  Chaudhry, Muhammad  Maxwell, Kyle  Upadhyaya, Siddhi  Drummond, Christopher A  Tian, Jiang  Filipiak, Wanda E  Saunders, Thomas L  Shapiro, Joseph I  Joe, Bina  Cooper, Christopher J 
Citation: Haller ST, etal., Kidney Int. 2017 Feb;91(2):365-374. doi: 10.1016/j.kint.2016.08.015. Epub 2016 Sep 28.
RGD ID: 14398462
Pubmed: (View Article at PubMed) PMID:27692815
DOI: Full-text: DOI:10.1016/j.kint.2016.08.015

High blood pressure is a common cause of chronic kidney disease. Because CD40, a member of the tumor necrosis factor receptor family, has been linked to the progression of kidney disease in ischemic nephropathy, we studied the role of Cd40 in the development of hypertensive renal disease. The Cd40 gene was mutated in the Dahl S genetically hypertensive rat with renal disease by targeted-gene disruption using zinc-finger nuclease technology. These rats were then given low (0.3%) and high (2%) salt diets and compared. The resultant Cd40 mutants had significantly reduced levels of both urinary protein excretion (41.8 ± 3.1 mg/24 h vs. 103.7 ± 4.3 mg/24 h) and plasma creatinine (0.36 ± 0.05 mg/dl vs. 1.15 ± 0.19 mg/dl), with significantly higher creatinine clearance compared with the control S rats (3.04 ± 0.48 ml/min vs. 0.93 ± 0.15 ml/min), indicating renoprotection was conferred by mutation of the Cd40 locus. Furthermore, the Cd40 mutants had a significant attenuation in renal fibrosis, which persisted on the high salt diet. However, there was no difference in systolic blood pressure between the control and Cd40 mutant rats. Thus, these data serve as the first evidence for a direct link between Cd40 and hypertensive nephropathy. Hence, renal fibrosis is one of the underlying mechanisms by which Cd40 plays a crucial role in the development of hypertensive renal disease.



Gene Ontology Annotations    

Biological Process

Phenotype Annotations    

Mammalian Phenotype
Objects Annotated

Genes (Rattus norvegicus)
Cd40  (CD40 molecule)
Cd40em1Uthal  (CD40 molecule; ZFN induced mutant 1, Uthal)

Strains
SS-Cd40em1Uthal-/-  (NA)


Additional Information