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A systems biology network analysis of nutri(epi)genomic changes in endothelial cells exposed to epicatechin metabolites.
Milenkovic, Dragan; Berghe, Wim Vanden; Morand, Christine; Claude, Sylvain; van de Sandt, Annette; Gorressen, Simone; Monfoulet, Laurent-Emmanuel; Chirumamilla, Chandra S; Declerck, Ken; Szic, Katarzyna Szarc Vel; Lahtela-Kakkonen, Maija; Gerhauser, Clarissa; Merx, Marc W; Kelm, Malte.
Afiliação
  • Milenkovic D; INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand; Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000, Clermont-Ferrand, France. dragan.milenkovic@inra.fr.
  • Berghe WV; Department of Internal Medicine, Division of Cardiovascular Medicine, School of Medicine, University of California Davis, Davis, California, 95616, United States of America. dragan.milenkovic@inra.fr.
  • Morand C; PPES, Department of Biomedical Sciences, University of Antwerp (UA), Wilrijk, Belgium.
  • Claude S; L-GEST, Department of Biochemistry and Microbiology, University of Gent, Ghent, Belgium.
  • van de Sandt A; INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand; Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000, Clermont-Ferrand, France.
  • Gorressen S; INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand; Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000, Clermont-Ferrand, France.
  • Monfoulet LE; Division of Cardiology, Pulmonology, and Vascular Medicine, Medical Faculty, University Hospital Düsseldorf, Düsseldorf, Germany.
  • Chirumamilla CS; Division of Cardiology, Pulmonology, and Vascular Medicine, Medical Faculty, University Hospital Düsseldorf, Düsseldorf, Germany.
  • Declerck K; INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand; Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000, Clermont-Ferrand, France.
  • Szic KSV; PPES, Department of Biomedical Sciences, University of Antwerp (UA), Wilrijk, Belgium.
  • Lahtela-Kakkonen M; PPES, Department of Biomedical Sciences, University of Antwerp (UA), Wilrijk, Belgium.
  • Gerhauser C; PPES, Department of Biomedical Sciences, University of Antwerp (UA), Wilrijk, Belgium.
  • Merx MW; School of Pharmacy, University of Eastern Finland, Kuopio, Finland.
  • Kelm M; Division of Epigenomics and Cancer Risk Factors, DKFZ, Heidelberg, Germany.
Sci Rep ; 8(1): 15487, 2018 10 19.
Article em En | MEDLINE | ID: mdl-30341379
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Catequina / Biologia de Sistemas / Nutrigenômica / Metaboloma / Epigenômica / Células Endoteliais da Veia Umbilical Humana Limite: Animals / Humans / Male Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Catequina / Biologia de Sistemas / Nutrigenômica / Metaboloma / Epigenômica / Células Endoteliais da Veia Umbilical Humana Limite: Animals / Humans / Male Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França