Phenolic Compounds of Red Wine Aglianico del Vulture Modulate the Functional Activity of Macrophages via Inhibition of NF-κB and the Citrate Pathway

Author:

Santarsiero Anna1ORCID,Convertini Paolo1ORCID,Vassallo Antonio1ORCID,Santoro Valentina2,Todisco Simona1ORCID,Iacobazzi Dominga3,Fondufe-Mittendorf Yvonne4ORCID,Martelli Giuseppe1ORCID,de Oliveira Marcos R.5ORCID,Montanaro Rosangela1,Brancaleone Vincenzo1ORCID,Stöckl Johannes6ORCID,Infantino Vittoria1ORCID

Affiliation:

1. Department of Science, University of Basilicata, Viale dell’Ateneo Lucano 10, 85100 Potenza, Italy

2. Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, 84084 Salerno, Italy

3. Bristol Heart Institute, Bristol Medical School, University of Bristol, Bristol BS2 8HW, UK

4. Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536, USA

5. Departamento de Bioquímica Rua Ramiro Barcelos, Universidade Federal do Rio Grande do Sul (UFRGS), 2600 Anexo Santa Cecília, Porto Alegre, RS, Brazil

6. Institute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, 1090 Vienna, Austria

Abstract

Phenolic compounds of red wine powder (RWP) extracted from the Italian red wine Aglianico del Vulture have been investigated for the potential immunomodulatory and anti-inflammatory capacity on human macrophages. These compounds reduce the secretion of IL-1β, IL-6, and TNF-α proinflammatory cytokines and increase the release of IL-10 anti-inflammatory cytokine induced by lipopolysaccharide (LPS). In addition, RWP restores Annexin A1 levels, thus involving activation of proresolutive pathways. Noteworthy, RWP lowers NF-κB protein levels, promoter activity, and nuclear translocation. As a consequence of NF-κB inhibition, reduced promoter activities of SLC25A1—encoding the mitochondrial citrate carrier (CIC)—and ATP citrate lyase (ACLY) metabolic genes have been observed. CIC, ACLY, and citrate are components of the citrate pathway: in LPS-activated macrophages, the mitochondrial citrate is exported by CIC into the cytosol where it is cleaved by ACLY in oxaloacetate and acetyl-CoA, precursors for ROS, NO⋅, and PGE2 inflammatory mediators. We identify the citrate pathway as a RWP target in carrying out its anti-inflammatory activity since RWP reduces CIC and ACLY protein levels, ACLY enzymatic activity, the cytosolic citrate concentration, and in turn ROS, NO⋅, PGE2, and histone acetylation levels. Overall findings suggest that RWP potentially restores macrophage homeostasis by suppressing inflammatory pathways and activating proresolutive processes.

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

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