Sphingosine-1-phosphate: A bioactive lipid that confers high-density lipoprotein with vasculoprotection mediated by nitric oxide and prostacyclin


Por: Rodriguez, C, Gonzalez-Diez, M, Badimon, L, Martinez-Gonzalez, J

Publicada: 1 abr 2009
Resumen:
Sphingosine-1-phosphate (S1P) is a bioactive lipid generated in the intracellular membranes from the metabolism of sphingomyelin. Once secreted/exported by cells of haematopoietic origin and vascular cells S1P interacts with plasma proteins and accumulates in high-density lipoprotein (HDL). Growing evidence indicates that HDL-associated S1P is responsible for the beneficial effects of these lipoproteins on vasorelaxation, cell survival, cell adhesiveness, angiogenesis and synthesis of two powerful endogenous anti-atherogenic and anti-thrombotic molecules such as nitric oxide (NO) and prostacyclin (PGI(2)). It's likely that vascular effects of HDL-S1P are regulated by the local expression of S1P receptors. Five G protein-coupled receptors (S1P, to S1P(5)), with differential expression patterns and dissimilar coupling mechanism to G protein subunits, have been identified in the vasculature. This review is focused on the central role of S1P as a bioactive component that confers vasculoprotective properties to HDL by eliciting a wide range of biological responses on endothelial and smooth muscle cells largely dependent on the up-regulation of NO and prostacyclin.

Filiaciones:
Rodriguez, C:
 Hosp Santa Creu & Sant Pau, Ctr Invest Cardiovasc, CSIC, ICCC, E-08025 Barcelona, Spain

Gonzalez-Diez, M:
 Hosp Santa Creu & Sant Pau, Ctr Invest Cardiovasc, CSIC, ICCC, E-08025 Barcelona, Spain

Badimon, L:
 Hosp Santa Creu & Sant Pau, Ctr Invest Cardiovasc, CSIC, ICCC, E-08025 Barcelona, Spain

Martinez-Gonzalez, J:
 Hosp Santa Creu & Sant Pau, Ctr Invest Cardiovasc, CSIC, ICCC, E-08025 Barcelona, Spain
ISSN: 03406245





THROMBOSIS AND HAEMOSTASIS
Editorial
GEORG THIEME VERLAG KG, RUDIGERSTR 14, D-70469 STUTTGART, GERMANY, Alemania
Tipo de documento: Review
Volumen: 101 Número: 4
Páginas: 665-673
WOS Id: 000265333600011
ID de PubMed: 19350109

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