Induction of reactive oxygen species by mechanical stretch drives endothelin production in neonatal pig renal epithelial cells

• Published in: Redox biology Vol. 55; p. 102394
• Main Authors: Kumar, Ravi, Soni, Hitesh, Afolabi, Jeremiah M., Kanthakumar, Praghalathan, Mankuzhy, Pratheesh D., Iwhiwhu, Samson A., Adebiyi, Adebowale
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.09.2022; Elsevier
• Subjects: Acute kidney injury; Endothelin; Endothelin converting enzyme; Hydrogen peroxide; Mechanical stretch; Neonatal pigs; Research Paper; Urinary tract obstruction; Neonatal pigs; Hydrogen peroxide; Endothelin; PT; IHC; Endothelin converting enzyme; rUUO; LVGCC; H2O2; RVR; DMEM; FBS; tRBF; Urinary tract obstruction; AKI; SR; TRPC3; Acute kidney injury; ECE; SOC; ROC; qRT-PCR; SMC; DAG; IP3; UUO; ET; Mechanical stretch; ROS; MAP
• ISSN: 2213-2317; 2213-2317
• DOI: 10.1016/j.redox.2022.102394

Vasoactive endothelin (ET) is generated by ET converting enzyme (ECE)-induced proteolytic processing of pro-molecule big ET to biologically active peptides. H2O2 has been shown to increase the expression of ECE1 via transactivation of its promoter. The present study demonstrates that H2O2 triggered ECE1-dependent ET1-3 production in neonatal pig proximal tubule (PT) epithelial cells. A uniaxial stretch of PT cells decreased catalase, increased NADPH oxidase (NOX)2 and NOX4, and increased H2O2 levels. Stretch also increased cellular ECE1, an effect reversed by EUK-134 (a synthetic superoxide dismutase/catalase mimetic), NOX inhibitor apocynin, and siRNA-mediated knockdown of NOX2 and NOX4. Short-term unilateral ureteral obstruction (UUO), an inducer of renal tubular cell stretch and oxidative stress, increased renal ET1-3 generation and vascular resistance (RVR) in neonatal pigs. Despite removing the obstruction, UUO-induced increase in RVR persisted, resulting in early acute kidney injury (AKI). ET receptor (ETR)-operated Ca2+ entry in renal microvascular smooth muscle (SM) via transient receptor potential channel 3 (TRPC3) channels reduced renal blood flow and increased RVR. Although acute reversible UUO (rUUO) did not change protein expression levels of ETR and TRPC3 in renal microvessels, inhibition of ECE1, ETR, and TRPC3 protected against renal hypoperfusion, RVR increase, and early AKI. These data suggest that mechanical stretch-driven oxyradical generation stimulates ET production in neonatal pig renal epithelial cells. ET activates renal microvascular SM TRPC3, leading to persistent vasoconstriction and reduction in renal blood flow. These mechanisms may underlie rUUO-induced renal insufficiency in infants. [Display omitted]