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Projekt Druckansicht

Regulation of vascular permeability by sphingolipids

Fachliche Zuordnung Anatomie und Physiologie
Förderung Förderung von 2007 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 39051989
 
Erstellungsjahr 2009

Zusammenfassung der Projektergebnisse

Our major findings are summarized. Within minutes the PAF-induced stimulation of ASM leads to a decrease in endothelial NO production and an increase in endothelial calcium levels. The simultaneous decrease of the barrier protective NO and the increase of intracellular calcium via activation of the myosin light chain kinase leads to a sudden increase in vascular permeability. We hypothesize that the activation of the ASM and the ensuing ceramide production lead to a reorganization of caveolae that is required to assemble several proteins therein. The decreased NO production is explained by recruitment of caveolin-1 and eNOS into caveolae whose interaction keeps eNOS inactive in the membrane. The increase in endothelial calcium levels is explained by the recruitment of TRPC-channels (probably TRPC6) to caveolae. The anti-edematous eff ect of dexamethasone appears to be upstream of the activation of the ASM, off ering a novel explanation for this long known effect of steroids.

Projektbezogene Publikationen (Auswahl)

  • Mechanotransduction by TRP channels: general concepts and specifi c role in the vasculature. Cell Biochem Biophys
    Yin J, Kuebler WM
  • Sphingolipids in the lungs. Am J Respir Crit Care Med 178: 1100-1114
    Uhlig S, Gulbins E
  • 2008. Improved pulmonary function by acid sphingomyelinase inhibition in a newborn piglet lavage model. Am J Respir Crit Care Med 177: 1233-1241
    von Wistädt BP, CF, Klemm K, Winoto-Morbach S, Uhlig U, Schütze S, Adam D, Lachmann B, Uhlig S, Krause MF
  • 2009. Potent and selective inhibition of acid sphingomyelinase by bisphosphonates. Angew Chem Int Ed Engl 48: 7560-7563
    Roth AG, Drescher D, Yang Y, Redmer S, Uhlig S, Arenz C
 
 

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