11
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The flavonoid 4,4′-dimethoxychalcone promotes autophagy-dependent longevity across species

      research-article
      1 , 1 , 2 , 1 , 3 , 4 , 5 , 6 , 3 , 4 , 5 , 6 , 7 , 7 , 8 , 9 , 9 , 3 , 4 , 5 , 6 , 10 , 3 , 4 , 5 , 6 , 11 , 11 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 12 , 1 , 1 , 3 , 4 , 3 , 4 , 3 , 4 , 12 , 12 , 13 , 3 , 4 , 1 , 14 , 3 , 4 , 5 , 6 , 11 , 2 , 11 , 2 , 11 , 8 , 7 , 15 , 9 , 16 , 3 , 4 , 5 , 6 , 17 , 18 , , 1 , 13 ,
      Nature Communications
      Nature Publishing Group UK

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Ageing constitutes the most important risk factor for all major chronic ailments, including malignant, cardiovascular and neurodegenerative diseases. However, behavioural and pharmacological interventions with feasible potential to promote health upon ageing remain rare. Here we report the identification of the flavonoid 4,4′-dimethoxychalcone (DMC) as a natural compound with anti-ageing properties. External DMC administration extends the lifespan of yeast, worms and flies, decelerates senescence of human cell cultures, and protects mice from prolonged myocardial ischaemia. Concomitantly, DMC induces autophagy, which is essential for its cytoprotective effects from yeast to mice. This pro-autophagic response induces a conserved systemic change in metabolism, operates independently of TORC1 signalling and depends on specific GATA transcription factors. Notably, we identify DMC in the plant Angelica keiskei koidzumi, to which longevity- and health-promoting effects are ascribed in Asian traditional medicine. In summary, we have identified and mechanistically characterised the conserved longevity-promoting effects of a natural anti-ageing drug.

          Abstract

          Although ageing is the most important risk factor for chronic ailments, effective interventions remain rare. Here, the authors identify the flavonoid 4,4’-dimethoxychalcone and demonstrate that it extends lifespan and promotes health in multiple organisms by inducing autophagy.

          Related collections

          Most cited references39

          • Record: found
          • Abstract: not found
          • Article: not found

          Arterial and cardiac aging: major shareholders in cardiovascular disease enterprises: Part I: aging arteries: a "set up" for vascular disease.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast.

            Heterologous markers are important tools required for the molecular dissection of gene function in many organisms, including Saccharomyces cerevisiae. Moreover, the presence of gene families and isoenzymes often makes it necessary to delete more than one gene. We recently introduced a new and efficient gene disruption cassette for repeated use in budding yeast, which combines the heterologous dominant kan(r) resistance marker with a Cre/loxP-mediated marker removal procedure. Here we describe an additional set of four completely heterologous loxP-flanked marker cassettes carrying the genes URA3 and LEU2 from Kluyveromyces lactis, his5(+) from Schizosaccharomyces pombe and the dominant resistance marker ble(r) from the bacterial transposon Tn5, which confers resistance to the antibiotic phleomycin. All five loxP--marker gene--loxP gene disruption cassettes can be generated using the same pair of oligonucleotides and all can be used for gene disruption with high efficiency. For marker rescue we have created three additional Cre expression vectors carrying HIS3, TRP1 or ble(r) as the yeast selection marker. The set of disruption cassettes and Cre expression plasmids described here represents a significant further development of the marker rescue system, which is ideally suited to functional analysis of the yeast genome.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Aging and Autophagy in the Heart.

              The aging population is increasing in developed countries. Because the incidence of cardiac disease increases dramatically with age, it is important to understand the molecular mechanisms through which the heart becomes either more or less susceptible to stress. Cardiac aging is characterized by the presence of hypertrophy, fibrosis, and accumulation of misfolded proteins and dysfunctional mitochondria. Macroautophagy (hereafter referred to as autophagy) is a lysosome-dependent bulk degradation mechanism that is essential for intracellular protein and organelle quality control. Autophagy and autophagic flux are generally decreased in aging hearts, and murine autophagy loss-of-function models develop exacerbated cardiac dysfunction that is accompanied by the accumulation of misfolded proteins and dysfunctional organelles. On the contrary, stimulation of autophagy generally improves cardiac function in mouse models of protein aggregation by removing accumulated misfolded proteins, dysfunctional mitochondria, and damaged DNA, thereby improving the overall cellular environment and alleviating aging-associated pathology in the heart. Increasing lines of evidence suggest that autophagy is required for many mechanisms that mediate lifespan extension, such as caloric restriction, in various organisms. These results raise the exciting possibility that autophagy may play an important role in combating the adverse effects of aging in the heart. In this review, we discuss the role of autophagy in the heart during aging, how autophagy alleviates age-dependent changes in the heart, and how the level of autophagy in the aging heart can be restored.
                Bookmark

                Author and article information

                Contributors
                kroemer@orange.fr
                frank.madeo@uni-graz.at
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                19 February 2019
                19 February 2019
                2019
                : 10
                : 651
                Affiliations
                [1 ]ISNI 0000000121539003, GRID grid.5110.5, Institute of Molecular Biosciences, NAWI Graz, , University of Graz, ; Graz, 8010 Austria
                [2 ]ISNI 0000 0000 8988 2476, GRID grid.11598.34, Division of Endocrinology and Diabetology, Department of Internal Medicine, , Medical University of Graz, ; Graz, 8036 Austria
                [3 ]GRID grid.417925.c, Equipe 11 labellisée Ligue contre le Cancer, , Centre de Recherche des Cordeliers, INSERM U 1138, ; Paris, France
                [4 ]ISNI 0000 0001 2284 9388, GRID grid.14925.3b, Metabolomics and Cell Biology Platforms, , Gustave Roussy Comprehensive Cancer Center, ; Villejuif, France
                [5 ]ISNI 0000 0004 1788 6194, GRID grid.469994.f, Université Paris Descartes, , Sorbonne Paris Cité, ; Paris, France
                [6 ]ISNI 0000 0001 2308 1657, GRID grid.462844.8, Université Pierre et Marie Curie, ; Paris, France
                [7 ]ISNI 0000 0004 0518 6318, GRID grid.435557.5, IUF - Leibniz Research Institute for Environmental Medicine, ; Düsseldorf, 40225 Germany
                [8 ]ISNI 0000 0000 8692 8176, GRID grid.469131.8, Department of Cell Biology and Molecular Medicine, , Rutgers New Jersey Medical School, ; Newark, NJ USA
                [9 ]ISNI 0000 0000 9116 4836, GRID grid.14095.39, Institute for Biology/Genetics, , Freie Universität Berlin, ; Berlin, 14195 Germany
                [10 ]Sotio a.c, 17000 Prague, Czech Republic
                [11 ]Joanneum Research Forschungsgesellschaft m.b.H., HEALTH, Institute for Biomedicine and Health Sciences, Graz, 8010 Austria
                [12 ]ISNI 0000 0000 8988 2476, GRID grid.11598.34, Department of Cardiology, , Medical University of Graz, ; Graz, 8036 Austria
                [13 ]GRID grid.452216.6, BioTechMed Graz, ; Graz, 8010 Austria
                [14 ]ISNI 0000 0004 0478 1713, GRID grid.8534.a, Department of Biology, , Université de Fribourg, ; Chemin du Musée 10, 1700 Fribourg, Switzerland
                [15 ]ISNI 0000 0001 2176 9917, GRID grid.411327.2, Institute for Clinical Chemistry and Laboratory Diagnostic, , Medical Faculty of the Heinrich Heine University, ; Moorenstrasse 5, 40225 Düsseldorf, Germany
                [16 ]ISNI 0000 0001 2218 4662, GRID grid.6363.0, NeuroCure, Charité, ; Berlin, 10117 Germany
                [17 ]GRID grid.414093.b, Pôle de Biologie, , Hôpital Européen Georges Pompidou, ; Paris, France
                [18 ]ISNI 0000 0000 9241 5705, GRID grid.24381.3c, Karolinska Institute, Department of Women’s and Children’s Health, , Karolinska University Hospital, ; Stockholm, Sweden
                Author information
                http://orcid.org/0000-0003-2249-944X
                http://orcid.org/0000-0002-0756-0014
                http://orcid.org/0000-0003-3559-1130
                http://orcid.org/0000-0002-4419-6821
                http://orcid.org/0000-0002-9453-4614
                http://orcid.org/0000-0002-6081-9558
                http://orcid.org/0000-0001-8718-4321
                Article
                8555
                10.1038/s41467-019-08555-w
                6381180
                30783116
                3124b496-4043-47bd-a5c8-86a8a207eb67
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 30 October 2018
                : 11 January 2019
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                Uncategorized

                Comments

                Comment on this article