Worsening of obesity and metabolic status yields similar molecular adaptations in human subcutaneous and visceral adipose tissue: decreased metabolism and increased immune response

Autor: Nathalie Viguerie, Vladimir Stich, Petra Šrámková, Michaela Siklova-Vitkova, Anne Bouloumié, Dominique Langin, Zuzana Kovacova, Eva Klimcakova, Adriana Márquez-Quiñones, Balbine Roussel, Jindra Hejnova, Michaela Kovacikova, Marion Combes
Přispěvatelé: Franco-czech Laboratory for clinical research on obesity, Charles University [Prague] (CU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut de médecine moléculaire de Rangueil (I2MR), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Fédératif de Recherche 150, Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, OB Clinic, AVENIR team 'Vascular network, progenitor cells and immune cells', Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-IFR150-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Toulouse III - Paul Sabatier (UT3), Laboratoire de Biochimie, CHU Toulouse [Toulouse]-Institut de Biologie de Purpan, Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées- Institut Fédératif de Recherche Bio-médicale Institution (IFR150)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées- Institut Fédératif de Recherche Bio-médicale Institution (IFR150)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Toulouse III - Paul Sabatier (UT3), 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), Simon, Marie Francoise
Rok vydání: 2010
Předmět:
Endocrinology
Diabetes and Metabolism

Clinical Biochemistry
Adipose tissue
Gene Expression
Overweight
Biochemistry
MESH: Glucose Clamp Technique
MESH: Down-Regulation
0302 clinical medicine
Endocrinology
MESH: Metabolic Syndrome X
MESH: Obesity
MESH: Aged
Metabolic Syndrome
0303 health sciences
MESH: Middle Aged
Glucose clamp technique
Middle Aged
MESH: Insulin Resistance
Female
medicine.symptom
Adult
medicine.medical_specialty
MESH: Gene Expression
Subcutaneous Fat
Down-Regulation
030209 endocrinology & metabolism
Context (language use)
Biology
Intra-Abdominal Fat
03 medical and health sciences
Insulin resistance
MESH: Subcutaneous Fat
Internal medicine
medicine
Humans
Obesity
MESH: Intra-Abdominal Fat
030304 developmental biology
Aged
MESH: Humans
Biochemistry (medical)
nutritional and metabolic diseases
MESH: Adult
medicine.disease
Gene expression profiling
Glucose Clamp Technique
Metabolic syndrome
Insulin Resistance
MESH: Female
Zdroj: Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2011, 96 (1), pp.E73-82. ⟨10.1210/jc.2010-1575⟩
Journal of Clinical Endocrinology and Metabolism, 2011, 96 (1), pp.E73-82. ⟨10.1210/jc.2010-1575⟩
ISSN: 1945-7197
0021-972X
DOI: 10.1210/jc.2010-1575⟩
Popis: Context: It is not known whether biological differences reported between sc adipose tissue (SAT) and visceral adipose tissue (VAT) depots underlie the pathogenicity of visceral fat. Objective: We compared SAT and VAT gene expression according to obesity, visceral fat accumulation, insulin resistance, and presence of the metabolic syndrome. Design: Subjects were assigned into four groups (lean, overweight, obese, and obese with metabolic syndrome). Setting: Subjects were recruited at a university hospital. Patients: Thirty-two women were included. Main Outcome Measures: Anthropometric measurements, euglycemic-hyperinsulinemic clamps, blood analyses, and computed tomography scans were performed, and paired samples of SAT and VAT were obtained for DNA microarray-based gene expression profiling. Results: Considering the two fat depots together, 1125 genes were more and 1025 genes were less expressed in lean compared with metabolic syndrome subjects. Functional annotation clustering showed, from lean to metabolic syndrome subjects, progressive down-regulation of metabolic pathways including branched-chain amino acid, fatty acid, carbohydrate, and mitochondrial energy metabolism and up-regulation of immune response genes involved in toll-like receptor, TNF, nuclear factor-κB, and apoptosis pathways. Metabolism and immune response genes showed an opposite correlation with fat mass, fat distribution, or insulin resistance indices. These associations were similar in SAT and VAT, although about 1000 genes showed differential expression between SAT and VAT. Conclusions: The increase in adiposity and the worsening of metabolic status are associated with a coordinated down-regulation of metabolism-related and up-regulation of immune response-related gene expression. Molecular adaptations in SAT prove as discriminating as those in VAT.
Databáze: OpenAIRE