Abstract | OBJECTIVE: METHODS AND RESULTS: We performed gain-of-function and loss-of-function studies to investigate the role of GV sPLA2 in atherogenesis in LDL receptor-deficient mice. Compared with control mice, animals overexpressing GV sPLA2 by retrovirus-mediated gene transfer had a 2.7 fold increase in lesion area in the ascending region of the aortic root. Increased atherosclerosis was associated with an increase in lesional collagen deposition in the same region. Mice deficient in bone marrow-derived GV sPLA2 had a 36% reduction in atherosclerosis in the aortic arch/thoracic aorta. CONCLUSIONS: Our data in mouse models provide the first in vivo evidence that GV sPLA2 contributes to atherosclerotic processes, and draw attention to this enzyme as an attractive target for the treatment of atherosclerotic disease.
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Authors | Meredith A Bostrom, Boris B Boyanovsky, Craig T Jordan, Marilyn P Wadsworth, Douglas J Taatjes, Frederick C de Beer, Nancy R Webb |
Journal | Arteriosclerosis, thrombosis, and vascular biology
(Arterioscler Thromb Vasc Biol)
Vol. 27
Issue 3
Pg. 600-6
(Mar 2007)
ISSN: 1524-4636 [Electronic] United States |
PMID | 17204667
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Lipoproteins
- Receptors, LDL
- Phospholipases A
- Group V Phospholipases A2
- PLA2G5 protein, human
- Phospholipases A2
- Pla2g5 protein, mouse
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Topics |
- Animals
- Atherosclerosis
(enzymology)
- Disease Models, Animal
- Female
- Gene Expression Regulation
- Group V Phospholipases A2
- Lipid Metabolism
(physiology)
- Lipoproteins
(metabolism)
- Mice
- Mice, Inbred C57BL
- Mice, Transgenic
- Phospholipases A
(genetics, metabolism)
- Phospholipases A2
- Receptors, LDL
(deficiency)
- Reference Values
- Reverse Transcriptase Polymerase Chain Reaction
- Sensitivity and Specificity
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