Cyclooxygenase-2, prostaglandin E2, and prostanoid receptor EP2 in fluid flow shear stress-mediated injury in the solitary kidney

• Published in: American journal of physiology. Renal physiology 2014-12, Vol.307 (12), p.F1323-F1333
• Main Authors: Srivastava, Tarak, Alon, Uri S, Cudmore, Patricia A, Tarakji, Belal, Kats, Alexander, Garola, Robert E, Duncan, R Scott, McCarthy, Ellen T, Sharma, Ram, Johnson, Mark L, Bonewald, Lynda F, El-Meanawy, Ashraf, Savin, Virginia J, Sharma, Mukut
• Format: Article
• Language: English
• Subjects: Albuminuria - enzymology; Albuminuria - physiopathology; Animals; Cell Line; Cyclooxygenase 2 - genetics; Cyclooxygenase 2 - metabolism; Cyclooxygenase Inhibitors - pharmacology; Dinoprostone - metabolism; Disease Models, Animal; Kidney Glomerulus - blood supply; Kidney Glomerulus - drug effects; Kidney Glomerulus - enzymology; Kidney Glomerulus - pathology; Male; Mice; Mice, 129 Strain; Nephrectomy; Podocytes - metabolism; Podocytes - pathology; Receptors, Prostaglandin E, EP2 Subtype - genetics; Receptors, Prostaglandin E, EP2 Subtype - metabolism; Renal Circulation - drug effects; Renal Insufficiency, Chronic - enzymology; Renal Insufficiency, Chronic - etiology; Renal Insufficiency, Chronic - genetics; Renal Insufficiency, Chronic - pathology; Renal Insufficiency, Chronic - physiopathology; RNA, Messenger - metabolism; Signal Transduction; Stress, Mechanical; Time Factors; Up-Regulation
• ISSN: 1522-1466
• DOI: 10.1152/ajprenal.00335.2014

Hyperfiltration subjects podocytes to increased tensile stress and fluid flow shear stress (FFSS). We showed a 1.5- to 2.0-fold increase in FFSS in uninephrectomized animals and altered podocyte actin cytoskeleton and increased synthesis of prostaglandin E2 (PGE2) following in vitro application of FFSS. We hypothesized that increased FFSS mediates cellular changes through specific receptors of PGE2. Presently, we studied the effect of FFSS on cultured podocytes and decapsulated isolated glomeruli in vitro, and on solitary kidney in uninephrectomized sv129 mice. In cultured podocytes, FFSS resulted in increased gene and protein expression of cyclooxygenase (COX)-2 but not COX-1, prostanoid receptor EP2 but not EP4, and increased synthesis and secretion of PGE2, which were effectively blocked by indomethacin. Next, we developed a special flow chamber for applying FFSS to isolated glomeruli to determine its effect on an intact glomerular filtration barrier by measuring change in albumin permeability (Palb) in vitro. FFSS caused an increase in Palb that was blocked by indomethacin (P < 0.001). Finally, we show that unilateral nephrectomy in sv129 mice resulted in glomerular hypertrophy (P = 0.006), increased glomerular expression of COX-2 (P < 0.001) and EP2 (P = 0.039), and increased urinary albumin excretion (P = 0.001). Activation of the COX-2-PGE2-EP2 axis appears to be a specific response to FFSS in podocytes and provides a mechanistic basis for alteration in podocyte structure and the glomerular filtration barrier, leading to albuminuria in hyperfiltration-mediated kidney injury. The COX-2-PGE2-EP2 axis is a potential target for developing specific interventions to ameliorate the effects of hyperfiltration-mediated kidney injury in the progression of chronic kidney disease.