Articles producció científica> Medicina i Cirurgia

Adipose tissue glycogen accumulation is associated with obesity-linked inflammation in humans

  • Dades identificatives

    Identificador: imarina:5129347
    Autors:
    Ceperuelo-Mallafre, VictoriaEjarque, MiriamSerena, CarolinaDuran, XavierMontori-Grau, MartaAngel Rodriguez, MiguelYanes, OscarNunez-Roa, CatalinaRoche, KellyPuthanveetil, PrasanthGarrido-Sanchez, LourdesSaez, EnriqueTinahones, Francisco JGarcia-Roves, Pablo MMa Gomez-Foix, AnnaSaltiel, Alan RVendrell, JoanFernandez-Veledo, Sonia
    Resum:
    Objective: Glycogen metabolism has emerged as a mediator in the control of energy homeostasis and studies in murine models reveal that adipose tissue might contain glycogen stores. Here we investigated the physio(patho)logical role of glycogen in human adipose tissue in the context of obesity and insulin resistance. Methods: We studied glucose metabolic flux of hypoxic human adipoctyes by nuclear magnetic resonance and mass spectrometry-based metabolic approaches. Glycogen synthesis and glycogen content in response to hypoxia was analyzed in human adipocytes and macrophages. To explore the metabolic effects of enforced glycogen deposition in adipocytes and macrophages, we overexpressed PTG, the only glycogen-associated regulatory subunit (PP1-GTS) reported in murine adipocytes. Adipose tissue gene expression analysis was performed on wild type and homozygous PTG KO male mice. Finally, glycogen metabolism gene expression and glycogen accumulation was analyzed in adipose tissue, mature adipocytes and resident macrophages from lean and obese subjects with different degrees of insulin resistance in 2 independent cohorts. Results: We show that hypoxia modulates glucose metabolic flux in human adipocytes and macrophages and promotes glycogenesis. Enforced glycogen deposition by overexpression of PTG re-orients adipocyte secretion to a pro-inflammatory response linked to insulin resistance and monocyte/lymphocyte migration. Furthermore, glycogen accumulation is associated with inhibition of mTORC1 signaling and increased basal autophagy flux, correlating with greater leptin release in glycogen-loaded adipocytes. PTG-KO mice have reduced expression of key inflammatory genes in adipose tissue and PTG overexpression in M0 macrophages induces a pro-inflammatory and glycolytic M1 p
  • Altres:

    Autor segons l'article: Ceperuelo-Mallafre, Victoria; Ejarque, Miriam; Serena, Carolina; Duran, Xavier; Montori-Grau, Marta; Angel Rodriguez, Miguel; Yanes, Oscar; Nunez-Roa, Catalina; Roche, Kelly; Puthanveetil, Prasanth; Garrido-Sanchez, Lourdes; Saez, Enrique; Tinahones, Francisco J; Garcia-Roves, Pablo M; Ma Gomez-Foix, Anna; Saltiel, Alan R; Vendrell, Joan; Fernandez-Veledo, Sonia
    Departament: Ciències Mèdiques Bàsiques Medicina i Cirurgia Enginyeria Electrònica, Elèctrica i Automàtica
    Autor/s de la URV: Ceperuelo Mallafré, Maria Victoria / Fernandez Veledo, Sonia / Serena Perelló, Carolina / Vendrell Ortega, Juan José / Yanes Torrado, Óscar
    Paraules clau: Targeting subunits Retinal-pigment epithelium Proinflammatory cytokine Obesity Necrosis-factor-alpha Macrophage Lipid-metabolism Insulin-resistance Insulin resistance Glycogen Glucose-transport Endoplasmic-reticulum stress Diabetes Binding domain Autophagy Adipose tissue Adipocyte Activated protein-kinase macrophage insulin resistance glycogen autophagy adipocyte
    Resum: Objective: Glycogen metabolism has emerged as a mediator in the control of energy homeostasis and studies in murine models reveal that adipose tissue might contain glycogen stores. Here we investigated the physio(patho)logical role of glycogen in human adipose tissue in the context of obesity and insulin resistance. Methods: We studied glucose metabolic flux of hypoxic human adipoctyes by nuclear magnetic resonance and mass spectrometry-based metabolic approaches. Glycogen synthesis and glycogen content in response to hypoxia was analyzed in human adipocytes and macrophages. To explore the metabolic effects of enforced glycogen deposition in adipocytes and macrophages, we overexpressed PTG, the only glycogen-associated regulatory subunit (PP1-GTS) reported in murine adipocytes. Adipose tissue gene expression analysis was performed on wild type and homozygous PTG KO male mice. Finally, glycogen metabolism gene expression and glycogen accumulation was analyzed in adipose tissue, mature adipocytes and resident macrophages from lean and obese subjects with different degrees of insulin resistance in 2 independent cohorts. Results: We show that hypoxia modulates glucose metabolic flux in human adipocytes and macrophages and promotes glycogenesis. Enforced glycogen deposition by overexpression of PTG re-orients adipocyte secretion to a pro-inflammatory response linked to insulin resistance and monocyte/lymphocyte migration. Furthermore, glycogen accumulation is associated with inhibition of mTORC1 signaling and increased basal autophagy flux, correlating with greater leptin release in glycogen-loaded adipocytes. PTG-KO mice have reduced expression of key inflammatory genes in adipose tissue and PTG overexpression in M0 macrophages induces a pro-inflammatory and glycolytic M1 phenotype. Increased glycogen synthase expression correlates with glycogen deposition in subcutaneous adipose tissue of obese patients. Glycogen content in subcutaneous mature adipocytes is associated with BMI and leptin expression. Conclusion: Our data establish glycogen mishandling in adipose tissue as a potential key feature of inflammatory-related metabolic stress in human obesity.
    Àrees temàtiques: Molecular biology Endocrinology & metabolism Ciências biológicas ii Cell biology
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 22128778
    Adreça de correu electrònic de l'autor: oscar.yanes@urv.cat carolina.serena@urv.cat victoria.ceperuelo@urv.cat sonia.fernandez@urv.cat juanjose.vendrell@urv.cat
    Identificador de l'autor: 0000-0003-3695-7157 0000-0002-4460-9761 0000-0003-2906-3788 0000-0002-6994-6115
    Data d'alta del registre: 2024-10-12
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://www.sciencedirect.com/science/article/pii/S2212877815001969
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Molecular Metabolism. 5 (1): 5-18
    Referència de l'ítem segons les normes APA: Ceperuelo-Mallafre, Victoria; Ejarque, Miriam; Serena, Carolina; Duran, Xavier; Montori-Grau, Marta; Angel Rodriguez, Miguel; Yanes, Oscar; Nunez-Roa, (2016). Adipose tissue glycogen accumulation is associated with obesity-linked inflammation in humans. Molecular Metabolism, 5(1), 5-18. DOI: 10.1016/j.molmet.2015.10.001
    DOI de l'article: 10.1016/j.molmet.2015.10.001
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2016
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Cell Biology,Endocrinology & Metabolism,Molecular Biology
    Targeting subunits
    Retinal-pigment epithelium
    Proinflammatory cytokine
    Obesity
    Necrosis-factor-alpha
    Macrophage
    Lipid-metabolism
    Insulin-resistance
    Insulin resistance
    Glycogen
    Glucose-transport
    Endoplasmic-reticulum stress
    Diabetes
    Binding domain
    Autophagy
    Adipose tissue
    Adipocyte
    Activated protein-kinase
    macrophage
    insulin resistance
    glycogen
    autophagy
    adipocyte
    Molecular biology
    Endocrinology & metabolism
    Ciências biológicas ii
    Cell biology
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