A systems biology network analysis of nutri(epi)genomic changes in endothelial cells exposed to epicatechin metabolites

Published on Oct 19, 2018in Scientific Reports3.998
· DOI :10.1038/S41598-018-33959-X
Dragan Milenkovic32
Estimated H-index: 32
(UC Davis: University of California, Davis),
Wim Vanden Berghe56
Estimated H-index: 56
(UGent: Ghent University)
+ 11 AuthorsMalte Kelm90
Estimated H-index: 90
Sources
Abstract
Although vasculo-protective effects of flavan-3-ols are widely accepted today, their impact on endothelial cell functions and molecular mechanisms of action involved is not completely understood. The aim of this study was to characterize the potential endothelium-protective effects of circulating epicatechin metabolites and to define underlying mechanisms of action by an integrated systems biology approach. Reduced leukocyte rolling over vascular endothelium was observed following epicatechin supplementation in a mouse model of inflammation. Integrative pathway analysis of transcriptome, miRNome and epigenome profiles of endothelial cells exposed to epicatechin metabolites revealed that by acting at these different levels of regulation, metabolites affect cellular pathways involved in endothelial permeability and interaction with immune cells. In-vitro experiments on endothelial cells confirmed that epicatechin metabolites reduce monocyte adhesion and their transendothelial migration. Altogether, our in-vivo and in-vitro results support the outcome of a systems biology based network analysis which suggests that epicatechin metabolites mediate their vasculoprotective effects through dynamic regulation of endothelial cell monocyte adhesion and permeability. This study illustrates complex and multimodal mechanisms of action by which epicatechin modulate endothelial cell integrity.
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