Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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The effects of 3OC12-HSL on global gene expression in primary human aortic endothelial cells (HAEC).


ABSTRACT: Analysis of the effect of a bacterial quorum sensing molecule on in-vitro culture of human endothelial cells at gene expression levels. Objective: Chronic infection has long been postulated as a stimulus for atherogenesis. Pseudomonas aeruginosa infection has been associated with increased atherosclerosis in rats, and the bacteria produce a quorum sensing molecule 3-oxo-dodecynoyl-homoserine lactone (3OC12-HSL) that is critical for colonization and virulence. Paraoxonase 2 (PON2) hydrolyzes 3OC12-HSL and also protects against the effects of oxidized phospholipids thought to contribute to atherosclerosis. We now report the response of human aortic endothelial cells (HAEC) to 3OC12-HSL and oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine (Ox-PAPC) in relation to PON2 express

ORGANISM(S): Homo sapiens

SUBMITTER: Juyong Kim 

PROVIDER: E-GEOD-26295 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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