| Literature DB >> 32106110 |
Claire Laurens1,2,3, Anisha Parmar1,2, Enda Murphy4, Deborah Carper1,2, Benjamin Lair1,2, Pauline Maes3, Julie Vion1,2, Nathalie Boulet1,2, Coralie Fontaine1,2, Marie Marquès1,2, Dominique Larrouy1,2, Isabelle Harant1,2, Claire Thalamas1,5,6, Emilie Montastier1,2,6, Sylvie Caspar-Bauguil1,2,6, Virginie Bourlier1,2, Geneviève Tavernier1,2, Jean-Louis Grolleau6, Anne Bouloumié1,2, Dominique Langin1,2,6, Nathalie Viguerie1,2, Fabrice Bertile3, Stéphane Blanc3, Isabelle de Glisezinski1,2,6, Donal O'Gorman4, Cedric Moro1.
Abstract
We hypothesized that skeletal muscle contraction produces a cellular stress signal, triggering adipose tissue lipolysis to sustain fuel availability during exercise. The present study aimed at identifying exercise-regulated myokines, also known as exerkines, able to promote lipolysis. Human primary myotubes from lean healthy volunteers were submitted to electrical pulse stimulation (EPS) to mimic either acute intense or chronic moderate exercise. Conditioned media (CM) experiments with human adipocytes were performed. CM and human plasma samples were analyzed using unbiased proteomic screening and/or ELISA. Real-time qPCR was performed in cultured myotubes and muscle biopsy samples. CM from both acute intense and chronic moderate exercise increased basal lipolysis in human adipocytes. Growth and differentiation factor 15 (GDF15) gene expression and secretion increased rapidly upon skeletal muscle contraction. GDF15 protein was upregulated in CM from both acute and chronic exercise-stimulated myotubes. We further showed that physiological concentrations of recombinant GDF15 protein increased lipolysis in human adipose tissue, while blocking GDF15 with a neutralizing antibody abrogated EPS CM-mediated lipolysis. We herein provide the first evidence to our knowledge that GDF15 is a potentially novel exerkine produced by skeletal muscle contraction and able to target human adipose tissue to promote lipolysis.Entities:
Keywords: Adipose tissue; Metabolism; Skeletal muscle
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Year: 2020 PMID: 32106110 PMCID: PMC7213799 DOI: 10.1172/jci.insight.131870
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708