Aryl Hydrocarbon Receptor-Dependent and -Independent Pathways Mediate Curcumin Anti-Aging Effects
Vanessa Brinkmann,
Margherita Romeo,
Lucie Larigot,
Anne Hemmers,
Lisa Tschage,
Jennifer Kleinjohann,
Alfonso Schiavi,
Swantje Steinwachs,
Charlotte Esser,
Ralph Menzel,
Sara Giani Tagliabue,
Laura Bonati,
Fiona Cox,
Niloofar Ale-Agha,
Philipp Jakobs,
Joachim Altschmied,
Judith Haendeler,
Xavier Coumoul,
Natascia Ventura
Affiliations
Vanessa Brinkmann
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Margherita Romeo
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Lucie Larigot
Faculté des Sciences Fondamentales et Biomédicales, Université de Paris, 45 Rue des Saints-Pères, F-75006 Paris, France
Anne Hemmers
IUF—Leibniz Research Institute for Environmental Medicine, Auf’m Hennekamp 50, 40225 Düsseldorf, Germany
Lisa Tschage
IUF—Leibniz Research Institute for Environmental Medicine, Auf’m Hennekamp 50, 40225 Düsseldorf, Germany
Jennifer Kleinjohann
IUF—Leibniz Research Institute for Environmental Medicine, Auf’m Hennekamp 50, 40225 Düsseldorf, Germany
Alfonso Schiavi
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Swantje Steinwachs
IUF—Leibniz Research Institute for Environmental Medicine, Auf’m Hennekamp 50, 40225 Düsseldorf, Germany
Charlotte Esser
IUF—Leibniz Research Institute for Environmental Medicine, Auf’m Hennekamp 50, 40225 Düsseldorf, Germany
Ralph Menzel
Institute of Biology, Humboldt-University Berlin, Philippstr. 13, 10115 Berlin, Germany
Sara Giani Tagliabue
Department of Earth and Environmental Sciences, University of Milano-Bicocca, Piazza della Scienza 1, 20126 Milano, Italy
Laura Bonati
Department of Earth and Environmental Sciences, University of Milano-Bicocca, Piazza della Scienza 1, 20126 Milano, Italy
Fiona Cox
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Niloofar Ale-Agha
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Philipp Jakobs
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Joachim Altschmied
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Judith Haendeler
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
Xavier Coumoul
Faculté des Sciences Fondamentales et Biomédicales, Université de Paris, 45 Rue des Saints-Pères, F-75006 Paris, France
Natascia Ventura
Institute of Clinical Chemistry and Laboratory Diagnostic, Medical Faculty, Heinrich Heine University Düsseldorf, Moorenstr 5, 40225 Düsseldorf, Germany
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor whose activity can be modulated by polyphenols, such as curcumin. AhR and curcumin have evolutionarily conserved effects on aging. Here, we investigated whether and how the AhR mediates the anti-aging effects of curcumin across species. Using a combination of in vivo, in vitro, and in silico analyses, we demonstrated that curcumin has AhR-dependent or -independent effects in a context-specific manner. We found that in Caenorhabditis elegans, AhR mediates curcumin-induced lifespan extension, most likely through a ligand-independent inhibitory mechanism related to its antioxidant activity. Curcumin also showed AhR-independent anti-aging activities, such as protection against aggregation-prone proteins and oxidative stress in C. elegans and promotion of the migratory capacity of human primary endothelial cells. These AhR-independent effects are largely mediated by the Nrf2/SKN-1 pathway.