Journal article
The Differential Effect of Apyrase Treatment and hCD39 Overexpression on Chronic Renal Fibrosis after Ischemia-Reperfusion Injury
V Roberts, DJ Campbell, B Lu, J Chia, PJ Cowan, KM Dwyer
Transplantation | LIPPINCOTT WILLIAMS & WILKINS | Published : 2017
Abstract
Background Renal ischemia-reperfusion injury (IRI) leads to acute kidney injury and renal fibrosis. CD39 is a key purinergic enzyme in the hydrolysis of adenosine triphosphate (ATP) and increased CD39 enzymatic activity protects from acute IRI but its effect on renal fibrosis is not known. Methods Using a mouse model of unilateral renal IRI, the effects of increased CD39 activity (using soluble apyrase and mice expressing human CD39 transgene) on acute and chronic renal outcomes were examined. Nucleotide (ATP, adenosine diphosphate, adenosine monophosphate) and nucleoside (adenosine and inosine) levels were quantified by high-performance liquid chromatography. Soluble apyrase reduced acute r..
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Funding Acknowledgements
This work was supported by funding from Perpetual. St Vincent's Institute of Medical Research is supported in part by the Victorian Government's Operational Infrastructure Support Program.