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Sphingosine 1-phosphate (S1P) induces COX-2 expression and PGE2 formation via S1P receptor 2 in renal mesangial cells
Authors:Anja Völzke  Alexander Koch  Dagmar Meyer zu Heringdorf  Andrea Huwiler  Josef Pfeilschifter
Institution:1. Pharmazentrum Frankfurt/ZAFES, Klinikum der Johann Wolfgang Goethe-Universität, Theodor-Stern-Kai 7, D-60590 Frankfurt am Main, Germany;2. Institute of Pharmacology, University of Bern, Friedbühlstrasse 49, CH-3011 Bern, Switzerland
Abstract:Understanding the mechanisms of sphingosine 1-phosphate (S1P)-induced cyclooxygenase (COX)-2 expression and prostaglandin E2 (PGE2) formation in renal mesangial cells may provide potential therapeutic targets to treat inflammatory glomerular diseases. Thus, we evaluated the S1P-dependent signaling mechanisms which are responsible for enhanced COX-2 expression and PGE2 formation in rat mesangial cells under basal conditions. Furthermore, we investigated whether these mechanisms are operative in the presence of angiotensin II (Ang II) and of the pro-inflammatory cytokine interleukin-1β (IL-1β).
Keywords:AA  arachidonic acid  ActD  actinomycin D  Ang II  angiotensin II  CLX  celecoxib  COX  cyclooxygenase  HuR  human antigen R  IL-1β  interleukin-1β  MAPK  mitogen-activated protein kinase  MEK  MAPK kinase  NAC  N-acetylcystein  PGE2  prostaglandin E2  PLA2  group II phospholipase 2a  PTX  pertussis toxin  ROCK  Rho-dependent kinase  S1P  sphingosine 1-phosphat  S1PR  S1P receptors  SK  sphingosine kinase
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