Acyl chain-dependent effect of lysophosphatidylcholine on endothelial prostacyclin production
Autor: | Saša Frank, Wolfgang F. Graier, Akos Heinemann, Roland Malli, Gernot Desoye, Martin Hermansson, Andelko Hrzenjak, Horst Schweer, Michaela Tritscher, Pauli J. Ojala, Bernhard Watzer, Monika Riederer |
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Přispěvatelé: | Department of Biochemistry and Developmental Biology |
Rok vydání: | 2010 |
Předmět: |
Male
Endothelial lipase Prostacyclin 030204 cardiovascular system & hematology Phospholipase Biochemistry ACTIVATION Mice chemistry.chemical_compound 0302 clinical medicine Endocrinology 311 Basic medicine Research Articles Cells Cultured 0303 health sciences CULTURED HUMAN CYCLOOXYGENASE-2 EXPRESSION cyclooxygenase Lysophosphatidylcholine endothelial cell lipids (amino acids peptides and proteins) Arachidonic acid FATTY-ACIDS medicine.drug medicine.medical_specialty education LOW-DENSITY-LIPOPROTEIN SIGNAL-TRANSDUCTION QD415-436 Biology ADHESION MOLECULES 03 medical and health sciences PROTEIN-COUPLED RECEPTORS Phospholipase A2 In vivo Internal medicine arachidonic acid medicine Animals Humans RNA Messenger prostanoids 030304 developmental biology calcium Lysophosphatidylcholines Cell Biology Epoprostenol PHOSPHOLIPASE A(2) Mice Inbred C57BL chemistry Cyclooxygenase 2 CELLS biology.protein phospholipase A2 Endothelium Vascular Cyclooxygenase |
Zdroj: | Journal of Lipid Research, Vol 51, Iss 10, Pp 2957-2966 (2010) |
ISSN: | 0022-2275 |
Popis: | Previously we identified palmitoyl-lysophosphatidylcholine (16:0 LPC), linoleoyl-LPC (18:2 LPC), arachidonoyl-LPC (20:4 LPC), and oleoyl-LPC (18:1 LPC) as the most prominent LPC species generated by the action of endothelial lipase (EL) on high-density lipoprotein. In the present study, the impact of those LPC on prostacyclin (PGI(2)) production was examined in vitro in primary human aortic endothelial cells (HAEC) and in vivo in mice. Although 18:2 LPC was inactive, 16:0, 18:1, and 20:4 LPC induced PGI(2) production in HAEC by 1.4-, 3-, and 8.3-fold, respectively. LPC-elicited 6-keto PGF1α formation depended on both cyclooxygenase (COX)-1 and COX-2 and on the activity of cytosolic phospholipase type IVA (cPLA2). The LPC-induced, cPLA2-dependent (14)C-arachidonic acid (AA) release was increased 4.5-fold with 16:0, 2-fold with 18:1, and 2.7-fold with 20:4 LPC, respectively, and related to the ability of LPC to increase cytosolic Ca(2+) concentration. In vivo, LPC increased 6-keto PGF(1α) concentration in mouse plasma with a similar order of potency as found in HAEC. Our results indicate that the tested LPC species are capable of eliciting production of PGI(2), whereby the efficacy and the relative contribution of underlying mechanisms are strongly related to acyl-chain length and degree of saturation. |
Databáze: | OpenAIRE |
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