The role of lipoprotein-associated phospholipase A(2) in atherosclerosis may depend on its lipoprotein carrier in plasma
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Tellis, C. C.
Tselepis, A. D.
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Elsevier
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peer reviewed
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Biochimica Et Biophysica Acta-Molecular and Cell Biology of Lipids
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Platelet-activating factor (PAF) acetylhydrolase exhibits a Ca(2+)-independent phospholipase A(2) activity and degrades PAF as well as oxidized phospholipids (oxPL). Such phospholipids are accumulated in the artery wall and may play key roles in vascular inflammation and atherosclerosis. PAF-acetylhydrolase in plasma is complexed to lipoproteins; thus it is also referred to as lipoprotein-associated phospholipase A(2) (Lp-PLA(2)). Lp-PLA(2)A(2) is primarily associated with low-density lipoprotein (LDL), whereas a small proportion of circulating enzyme activity is also associated with high-density lipoprotein (HDL). The majority of the LDL-associated Lp-PLA(2) (LDL-Lp-PLA(2)) activity is bound to atherogenic small-dense LDL particles and it is a potential marker of these particles in plasma. The distribution of Lp-PLA(2) between LDL and HDL is altered in various types of dyslipidemias. It can be also influenced by the presence of lipoprotein (a) [Lp(a)] when plasma levels of this lipoprotein exceed 30 mg/dl. Several lines of evidence suggest that the role of plasma Lp-PLA(2) in atherosclerosis may depend on the type of lipoprotein particle with which this enzyme is associated. In this regard, data from large Caucasian population studies have shown an independent association between the plasma Lp-PILA(2) levels (which are mainly influenced by the levels of LDL-Lp-PLA(2)) and the risk of future cardiovascular events. On the contrary, several lines of evidence suggest that HDL-associated Lp-PLA(2) may substantially contribute to the HDL antiatherogenic activities. Recent studies have provided evidence that oxPL are preferentially sequestered on Lp(a) thus subjected to degradation by the Lp(a) -associated Lp-PLA(2). These data suggest that Lp(a) may be a potential scavenger of oxPL and provide new insights into the functional role of Lp(a) and the Lp(a)-associated Lp-PLA(2) in normal physiology as well as in inflammation and atherosclerosis. The present review is focused on recent advances concerning the Lp-PLA(2) structural characteristics, the molecular basis of the enzyme association with distinct lipoprotein subspecies, as well as the potential role of Lp-PLA(2) associated with different lipoprotein classes in atherosclerosis and cardiovascular disease. (C) 2009 Elsevier B.V. All rights reserved.
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Keywords
atherosclerosis, lp-pla(2), lipoprotein, inflammation, oxidized phospholipid, platelet-activating-factor, low-density-lipoprotein, factor-acetylhydrolase activity, acute coronary syndromes, human endothelial-cells, paf-degrading acetylhydrolase, b-containing lipoproteins, apolipoprotein-a-i, e-deficient mice, oxidized phospholipids
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<Go to ISI>://000266089200001
http://ac.els-cdn.com/S1388198109000651/1-s2.0-S1388198109000651-main.pdf?_tid=b1a43e0c3ae98918327dc1c0aeff58e7&acdnat=1333111900_d722f7892cb1821480e675a4ea5482d1
http://ac.els-cdn.com/S1388198109000651/1-s2.0-S1388198109000651-main.pdf?_tid=b1a43e0c3ae98918327dc1c0aeff58e7&acdnat=1333111900_d722f7892cb1821480e675a4ea5482d1
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en
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Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας