Cholesterol affects flow-stimulated cyclooxygenase-2 expression and prostanoid secretion in the cortical collecting duct
Authors:
- 1 June 2015
- journal article
- research article
- Published by American Physiological Society in American Journal of Physiology-Renal Physiology
- Vol. 308 (11) , F1229-F1237
Abstract
Essential hypertension (eHTN) is associated with hypercholesterolemia, but how cholesterol contributes to eHTN is unknown. Recent evidence demonstrates that short-term dietary cholesterol ingestion induces epithelial Na channel (ENaC)-dependent Na absorption with a subsequent rise in blood pressure (BP), implicating cholesterol in salt-sensitive HTN. Prostaglandin E2 (PGE2), an autocrine/paracrine molecule, is induced by flow in endothelia to vasodilate the vasculature and inhibit ENaC-dependent Na absorption in the renal collecting duct (CD), which reduce BP. We hypothesize that cholesterol suppresses flow-mediated cyclooxygenase-2 (COX-2) expression and PGE2 release in the CD, which, in turn, affects Na absorption. Cortical CDs (CCDs) were microperfused at 0, 1, and 5 nl·min−1·mm−1, and PGE2 release was measured. Secreted PGE2 was similar between no- and low-flow (151 ± 28 vs. 121 ± 48 pg·ml−1·mm−1) CCDs, but PGE2 was greatest from high-flow (578 ± 146 pg·ml−1·mm−1; P < 0.05) CCDs. Next, mice were fed either a 0 or 1% cholesterol diet, injected with saline to generate high urine flow rates, and CCDs were microdissected for PGE2 secretion. CCDs isolated from cholesterol-fed mice secreted less PGE2 and had a lower PGE2-generating capacity than CCDs isolated from control mice, implying cholesterol repressed flow-induced PGE2 synthesis. Next, cholesterol extraction in a CD cell line induced COX-2 expression and PGE2 release while cholesterol incorporation, conversely, suppressed their expression. Moreover, fluid shear stress (FSS) and cholesterol extraction induced COX-2 protein abundance via p38-dependent activation. Thus cellular cholesterol composition affects biomechanical signaling, which, in turn, affects FSS-mediated COX-2 expression and PGE2 release via a p38-dependent mechanism.Keywords
Funding Information
- VA Merit (1I01BX000388)
- NIH NIDDK P30 (DK079307)
- Bronx VA Research Foundation
This publication has 53 references indexed in Scilit:
- Regulation of renal NaCl and water transport by the ATP/UTP/P2Y2receptor systemAmerican Journal of Physiology-Renal Physiology, 2011
- Acute Cholesterol-induced Anti-natriuretic EffectsJournal of Biological Chemistry, 2011
- Fluid Shear Stress Induces Renal Epithelial Gene Expression through Polycystin-2-Dependent Trafficking of Extracellular Regulated KinaseNephron Physiology, 2010
- Cholesterol and Ion Channels2010
- Mechanoregulation of BK channel activity in the mammalian cortical collecting duct: role of protein kinases A and CAmerican Journal of Physiology-Renal Physiology, 2009
- Effect of aldosterone on BK channel expression in mammalian cortical collecting ductAmerican Journal of Physiology-Renal Physiology, 2008
- Primary cilia mediate mechanosensing in bone cells by a calcium-independent mechanismProceedings of the National Academy of Sciences, 2007
- Use of cyclodextrins to manipulate plasma membrane cholesterol content: Evidence, misconceptions and control strategiesBiochimica et Biophysica Acta (BBA) - Biomembranes, 2007
- Collecting duct-specific knockout of the endothelin B receptor causes hypertension and sodium retentionAmerican Journal of Physiology-Renal Physiology, 2006
- Transient Mechanoactivation of Neutral Sphingomyelinase in Caveolae to Generate CeramideJournal of Biological Chemistry, 2003