(556.16) Mechanical stretch-driven ROS generation stimulates endothelin production in neonatal pig renal epithelial and vascular endothelial cells

Poster Board Number: E108

Ravi Kumar (University of Tennessee Health Science Centre), Jeremiah Afolabi (University of Tennessee Health Science Centre), Praghalathan Kanthakumar (University of Tennessee Health Science Centre), Hitesh Soni (University of Tennessee Health Science Centre), Adebowale Adebiyi (University of Tennessee Health Science Centre)

The circulating level of endothelin (ET), a potent vasoactive peptide, decreases with postnatal age. ET is also of pathophysiological significance in the kidney. ET is generated via endothelin converting enzyme (ECE)-induced proteolytic processing of pro-molecule big ET to biologically active peptides. Hydrogen peroxide (H2O2), a reactive oxygen species (ROS), transactivates the promoter of ECE1. Oxyradicals contribute to kidney pathophysiology, but whether ROS regulates ET production in the kidneys remains unresolved. The present study shows that ECE1 is the predominant isoform in neonatal pig kidneys. We also demonstrated that H2O2 induces ECE1-dependent ET1-3 production in the neonatal pig renal proximal tubules (PT) and vascular endothelial cells (EC). A uniaxial stretch of neonatal pig PT and EC increased NADPH oxidase (NOX) 2 and 4 levels and stimulated H2O2 production. Mechanical stretch increased cellular ECE1 production in the PC and EC cells, which catalase mimetic EUK 134 and NOX inhibitor apocynin reversed. Mechanical stretch also triggered cellular ET1-3 generation in PT and EC. Mechanical stretch-induced ET1-3 production was attenuated by EUK 134, apocynin, and a selective ECE1 inhibitor CGS 35066. Short-term unilateral urinary tract obstruction (UUO), an inducer of the mechanical stretch of kidney cells and oxyradical production, increased ECE1-dependent ET1-3 production in neonatal pig kidneys. Despite removing the obstruction, acute UUO generated ROS, reduced kidney perfusion, and increased renal vascular resistance (RVR). UUO also elevated early biomarkers of acute kidney injury (AKI). Inhibition of ECE1 and ET receptors protected against UUO-induced increase in RVR and early AKI. These data suggest that mechanical stretch-driven ROS generation stimulates ET production in neonatal pig renal epithelial and vascular endothelial cells. ET then promotes AKI by causing renal hypoperfusion. This signaling pathway may underlie UUO-induced renal insufficiency in infants.

Dr. Adebiyi was supported by grants R01DK120595 and R01 DK127625 from the National Institute of Health.