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Network Analyses Reveal Negative Link Between Changes in Adipose Tissue GDF15 and BMI During Dietary-induced Weight Loss.
Imbert, Alyssa; Vialaneix, Nathalie; Marquis, Julien; Vion, Julie; Charpagne, Aline; Metairon, Sylviane; Laurens, Claire; Moro, Cedric; Boulet, Nathalie; Walter, Ondine; Lefebvre, Grégory; Hager, Jörg; Langin, Dominique; Saris, Wim H M; Astrup, Arne; Viguerie, Nathalie; Valsesia, Armand.
Afiliação
  • Imbert A; Institut National de la Santé et de la Recherche Médicale (Inserm), UMR1297, Institute of Metabolic and Cardiovascular Diseases, Team Metabolic Disorders and Diabesity, 31400, Toulouse, France.
  • Vialaneix N; Université de Toulouse, UMR1297, Institute of Metabolic and Cardiovascular Diseases, Paul Sabatier University, 31400, Toulouse, France.
  • Marquis J; INRAE, UR875 Mathématiques et Informatique Appliquées Toulouse, F-31326 Castanet-Tolosan, France.
  • Vion J; INRAE, UR875 Mathématiques et Informatique Appliquées Toulouse, F-31326 Castanet-Tolosan, France.
  • Charpagne A; Université de Lausanne, Genomic Technologies Facility, 1015, Lausanne, Switzerland.
  • Metairon S; Institut National de la Santé et de la Recherche Médicale (Inserm), UMR1297, Institute of Metabolic and Cardiovascular Diseases, Team Metabolic Disorders and Diabesity, 31400, Toulouse, France.
  • Laurens C; Université de Toulouse, UMR1297, Institute of Metabolic and Cardiovascular Diseases, Paul Sabatier University, 31400, Toulouse, France.
  • Moro C; Nestlé Institute of Health Sciences, Metabolic Health Department, 1015, Lausanne, Switzerland.
  • Boulet N; Nestlé Institute of Health Sciences, Metabolic Health Department, 1015, Lausanne, Switzerland.
  • Walter O; Institut National de la Santé et de la Recherche Médicale (Inserm), UMR1297, Institute of Metabolic and Cardiovascular Diseases, Team Metabolic Disorders and Diabesity, 31400, Toulouse, France.
  • Lefebvre G; Université de Toulouse, UMR1297, Institute of Metabolic and Cardiovascular Diseases, Paul Sabatier University, 31400, Toulouse, France.
  • Hager J; Institut National de la Santé et de la Recherche Médicale (Inserm), UMR1297, Institute of Metabolic and Cardiovascular Diseases, Team Metabolic Disorders and Diabesity, 31400, Toulouse, France.
  • Langin D; Université de Toulouse, UMR1297, Institute of Metabolic and Cardiovascular Diseases, Paul Sabatier University, 31400, Toulouse, France.
  • Saris WHM; Institut National de la Santé et de la Recherche Médicale (Inserm), UMR1297, Institute of Metabolic and Cardiovascular Diseases, Team Metabolic Disorders and Diabesity, 31400, Toulouse, France.
  • Astrup A; Institut National de la Santé et de la Recherche Médicale (Inserm), UMR1297, Institute of Metabolic and Cardiovascular Diseases, Team Adipose tissue, microbiota and cardiometabolic flexibility, 31400, Toulouse, France.
  • Viguerie N; Nestlé Institute of Health Sciences, Metabolic Health Department, 1015, Lausanne, Switzerland.
  • Valsesia A; Nestlé Institute of Health Sciences, Metabolic Health Department, 1015, Lausanne, Switzerland.
J Clin Endocrinol Metab ; 107(1): e130-e142, 2022 01 01.
Article em En | MEDLINE | ID: mdl-34415992
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Redução de Peso / Tecido Adiposo / Dieta Redutora / Redes Reguladoras de Genes / Fator 15 de Diferenciação de Crescimento / Transcriptoma / Obesidade Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Redução de Peso / Tecido Adiposo / Dieta Redutora / Redes Reguladoras de Genes / Fator 15 de Diferenciação de Crescimento / Transcriptoma / Obesidade Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França