Distinctiveness of secretory phospholipase A2 group IIA and V suggesting unique roles in atherosclerosis

被引:49
作者
Rosengren, Birgitta
Jonsson-Rylander, Ann-Cathrine
Peilot, Helena
Camejo, German
Hurt-Camejo, Eva [1 ]
机构
[1] AstraZeneca, R&D, S-43183 Molndal, Sweden
[2] Sahlgrens Univ Hosp, Wallenberg Lab, S-41345 Gothenburg, Sweden
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2006年 / 1761卷 / 11期
关键词
D O I
10.1016/j.bbalip.2006.06.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clinical observations strongly support an association of circulating levels of secretory phospholipases A(2) (sPLA(2)) in atherosclerotic cardiovascular disease (ACVD). Two modes of action can provide causal support for these statistical correlations. One is the action of the enzymes on circulating lipoproteins and the other is direct action on the lipoproteins once in the arterial extracellular intima. In this review we discuss results suggesting a distinct profile of characteristics related to localization, action on plasma lipoproteins and interaction with arterial proteoglycans for sPLA(2)-IIA and sPLA(2)-V. The differences observed indicate that these enzymes may contribute to atherosclerosis through dissimilar pathways. Furthermore, we comment on recent animal studies from our laboratory indicating that the expression of type V enzyme is up-regulated by genetically and nutritionally-induced dyslipidemias but not the group type IIA enzyme, which is well known to be up-regulated by acute inflammation. The results suggest that if similar up-regulation occurs in humans in response to hyperlipidemia, it may create a distinctive link between the group V enzyme and the disease. (c) 2006 Elsevier B.V. All rights reserved.
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页码:1301 / 1308
页数:8
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