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Growth and differentiation factor 15 is secreted by skeletal muscle during exercise and promotes lipolysis in humans
Claire Laurens, Anisha Parmar, Enda Murphy, Deborah Carper, Benjamin Lair, Pauline Maes, Julie Vion, Nathalie Boulet, Coralie Fontaine, Marie Marquès, Dominique Larrouy, Isabelle Harant, Claire Thalamas, Emilie Montastier, Sylvie Caspar-Bauguil, Virginie Bourlier, Geneviève Tavernier, Jean-Louis Grolleau, Anne Bouloumié, Dominique Langin, Nathalie Viguerie, Fabrice Bertile, Stéphane Blanc, Isabelle de Glisezinski, Donal O’Gorman, Cedric Moro
Claire Laurens, Anisha Parmar, Enda Murphy, Deborah Carper, Benjamin Lair, Pauline Maes, Julie Vion, Nathalie Boulet, Coralie Fontaine, Marie Marquès, Dominique Larrouy, Isabelle Harant, Claire Thalamas, Emilie Montastier, Sylvie Caspar-Bauguil, Virginie Bourlier, Geneviève Tavernier, Jean-Louis Grolleau, Anne Bouloumié, Dominique Langin, Nathalie Viguerie, Fabrice Bertile, Stéphane Blanc, Isabelle de Glisezinski, Donal O’Gorman, Cedric Moro
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Research Article Metabolism

Growth and differentiation factor 15 is secreted by skeletal muscle during exercise and promotes lipolysis in humans

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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.

Authors

Claire Laurens, Anisha Parmar, Enda Murphy, Deborah Carper, Benjamin Lair, Pauline Maes, Julie Vion, Nathalie Boulet, Coralie Fontaine, Marie Marquès, Dominique Larrouy, Isabelle Harant, Claire Thalamas, Emilie Montastier, Sylvie Caspar-Bauguil, Virginie Bourlier, Geneviève Tavernier, Jean-Louis Grolleau, Anne Bouloumié, Dominique Langin, Nathalie Viguerie, Fabrice Bertile, Stéphane Blanc, Isabelle de Glisezinski, Donal O’Gorman, Cedric Moro

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Figure 3

GDF15 gene expression changes in contracting skeletal muscle.

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GDF15 gene expression changes in contracting skeletal muscle.
(A) Time c...
(A) Time course of GDF15 mRNA level in acutely EPS-stimulated myotubes. Data are expressed as mean ± SEM (n = 6). **P < 0.01, ***P < 0.001 compared with control by 2-way ANOVA followed by a Bonferroni post hoc test. (B) GDF15 mRNA level in EPS3h-stimulated myotubes and (C) in EPS24h-stimulated myotubes. Data are expressed as mean ± SEM (n = 12). *P < 0.05, **P < 0.01 compared with control by 2-tailed unpaired Student’s t test. (D–F) GDF15 mRNA level changes in response to exercise mimetics: human myotubes cultured for 5 days were treated for 3 hours with (D) 10 μM forskolin, (E) 4 μM ionomycin, (F) and the PPARδ agonist GW0742 (100 nM). Data are expressed as mean ± SEM (n = 6). **P < 0.01, ***P < 0.001 compared with control by 2-tailed unpaired Student’s t test. (G) GDF15 mRNA level changes in the muscle vastus lateralis biopsy samples taken before and immediately after a 1-hour acute exercise bout in lean healthy volunteers (human study 1). Data are expressed as mean ± SEM (n = 18). ***P < 0.001 compared with control by 2-tailed paired Student’s t test.

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