Elevated expression of lipoprotein-associated phospholipase A2 in calcific aortic valve disease : implications for valve mineralization.

Authors: Mahmut, AblajanBoulanger, Marie-ChloéEl Husseini, DialaFournier, DominiqueBouchareb, RihabDesprés, Jean-PierrePibarot, PhilippeBossé, YohanMathieu, Patrick
Abstract: OBJECTIVES: This study sought to document the presence and role of lipoprotein-associated phospholipase A2 (Lp-PLA2) in calcific aortic valve disease (CAVD). BACKGROUND: CAVD is a chronic disorder characterized by pathological mineralization and remodeling. Studies have indicated that human CAVD tissues are infiltrated by lipids and that inflammation may play a role in the pathobiology. We hypothesized that Lp-PLA2 (encoded by the PLA2G7 gene) is expressed in CAVD and may play a role in the mineralization of valve interstitial cells. METHODS: We have documented the expression of the phospholipase A2 family of genes in aortic valves by using a transcriptomic assay. Messenger ribonucleic acid and protein expression were confirmed in aortic valves explanted from 60 patients by quantitative polymerase chain reaction and immunohistochemistry, respectively. The effect of lysophosphatidylcholine, the product of Lp-PLA2 activity, was documented on the mineralization of valve interstitial cell cultures. RESULTS: Transcriptomic analyses of CAVD and control nonmineralized aortic valves revealed that Lp-PLA2 was increased by 4.2-fold in mineralized aortic valves. Higher expression of Lp-PLA2 in stenotic aortic valves was confirmed by quantitative polymerase chain reaction, immunohistochemistry, and enzymatic Lp-PLA2 activity. The number of Lp-PLA2 transcripts correlated with several indexes of tissue remodeling. In vitro, lysophosphatidylcholine increased the expression of alkaline phosphatase, the ectonucleotide pyrophosphatase/phosphodiesterase 1 enzyme, sodium-dependent phosphate cotransporter 1 (encoded by the SLC20A1 gene), and osteopontin. We then showed that lysophosphatidylcholine-induced mineralization involved ectonucleotidase enzyme as well as apoptosis through a protein-kinase-A-dependent pathway. CONCLUSIONS: Together, these results demonstrated that Lp-PLA2 is highly expressed in CAVD, and it plays a role in the mineralization of valve interstitial cells. Further work is necessary to document whether Lp-PLA2 could be considered as a novel target in CAVD.
Document Type: Article de recherche
Issue Date: 11 February 2014
Open Access Date: Restricted access
Document version: VoR
Permalink: http://hdl.handle.net/20.500.11794/7248
This document was published in: Journal of the American College of Cardiology, Vol. 63 (5), 460–469 (2014)
http://dx.doi.org/10.1016/j.jacc.2013.05.105
Elsevier Biomedical
Alternative version: 10.1016/j.jacc.2013.05.105
http://www.ncbi.nlm.nih.gov/pubmed/24161325
Collection:Articles publiés dans des revues avec comité de lecture

Files in this item:
SizeFormat 
Mahmut2014-13886.pdf
1.91 MBAdobe PDF    Request a copy
All documents in CorpusUL are protected by Copyright Act of Canada.