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Network analyses reveal negative link between changes in adipose tissue GDF15 and BMI during dietary-induced weight loss

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  • معلومة اضافية
    • Contributors:
      Institut des Maladies Métaboliques et Casdiovasculaires (UPS/Inserm U1297 - I2MC); Université Toulouse III - Paul Sabatier (UT3); Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM); Unité de Mathématiques et Informatique Appliquées de Toulouse (MIAT INRAE); Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE); Université de Lausanne = University of Lausanne (UNIL); Nestlé Institute of Health Sciences SA Lausanne, Switzerland; Franco-czech Laboratory for clinical research on obesity; Institut National de la Santé et de la Recherche Médicale (INSERM)-Univerzita Karlova Praha, Česká republika = Charles University Prague, Czech Republic (UK); Laboratoire de Biochimie CHU Toulouse; Institut Fédératif de Biologie (IFB); Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Pôle Biologie CHU Toulouse; Centre Hospitalier Universitaire de Toulouse (CHU Toulouse); Maastricht University Medical Centre (MUMC); Maastricht University Maastricht; IT University of Copenhagen (ITU); Institut National de la Sante et de la Recherche Medicale (Inserm); Paul Sabatier University; Innovative Medicines Initiative Joint Undertaking115372; European CommissionFP6-513946 DiOGenes
    • بيانات النشر:
      HAL CCSD
      Endocrine Society
    • الموضوع:
      2022
    • Collection:
      Institut National de la Recherche Agronomique: ProdINRA
    • نبذة مختصرة :
      International audience ; Abstract Context Adipose tissue (AT) transcriptome studies provide holistic pictures of adaptation to weight and related bioclinical settings changes. Objective To implement AT gene expression profiling and investigate the link between changes in bioclinical parameters and AT gene expression during 3 steps of a 2-phase dietary intervention (DI). Methods AT transcriptome profiling was obtained from sequencing 1051 samples, corresponding to 556 distinct individuals enrolled in a weight loss intervention (8-week low-calorie diet (LCD) at 800 kcal/day) followed with a 6-month ad libitum randomized DI. Transcriptome profiles obtained with QuantSeq sequencing were benchmarked against Illumina RNAseq. Reverse transcription quantitative polymerase chain reaction was used to further confirm associations. Cell specificity was assessed using freshly isolated cells and THP-1 cell line. Results During LCD, 5 modules were found, of which 3 included at least 1 bioclinical variable. Change in body mass index (BMI) connected with changes in mRNA level of genes with inflammatory response signature. In this module, change in BMI was negatively associated with changes in expression of genes encoding secreted protein (GDF15, CCL3, and SPP1). Through all phases of the DI, change in GDF15 was connected to changes in SPP1, CCL3, LIPA and CD68. Further characterization showed that these genes were specific to macrophages (with LIPA, CD68 and GDF15 expressed in anti-inflammatory macrophages) and GDF15 also expressed in preadipocytes. Conclusion Network analyses identified a novel AT feature with GDF15 upregulated with calorie restriction induced weight loss, concomitantly to macrophage markers. In AT, GDF15 was expressed in preadipocytes and macrophages where it was a hallmark of anti-inflammatory cells.
    • Relation:
      info:eu-repo/semantics/altIdentifier/arxiv/2203.09356; hal-03540946; https://hal.inrae.fr/hal-03540946; https://hal.inrae.fr/hal-03540946/document; https://hal.inrae.fr/hal-03540946/file/imbert_etal_JCEM2022.pdf; ARXIV: 2203.09356; WOS: 000736051000022
    • الرقم المعرف:
      10.1210/clinem/dgab621
    • الدخول الالكتروني :
      https://hal.inrae.fr/hal-03540946
      https://hal.inrae.fr/hal-03540946/document
      https://hal.inrae.fr/hal-03540946/file/imbert_etal_JCEM2022.pdf
      https://doi.org/10.1210/clinem/dgab621
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.8D1F881