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PMID: 15522911 Published · ppublish English Clinical Trial Controlled Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Weight loss regulates inflammation-related genes in white adipose tissue of obese subjects.

Clément K, Viguerie N, Poitou C, Carette C, Pelloux V, Curat CA, Sicard A, Rome S, Benis A, Zucker JD, Vidal H, Laville M, Barsh GS, Basdevant A, Stich V, Cancello R, Langin D

Abstract

Adipose tissue produces inflammation and immunity molecules suspected to be involved in obesity-related complications. The pattern of expression and the nutritional regulation of these molecules in humans are poorly understood. We analyzed the gene expression profiles of subcutaneous white adipose tissue from 29 obese subjects during very low calorie diet (VLCD) using cDNA microarray and reverse transcription quantitative PCR. The patterns of expression were compared with that of 17 non-obese subjects. We determined whether the regulated genes were expressed in adipocytes or stromavascular fraction cells. Gene expression profiling identified 100 inflammation-related transcripts that are regulated in obese individuals when eating a 28 day VLCD but not a 2 day VLCD. Cluster analysis showed that the pattern of gene expression in obese subjects after 28 day VLCD was closer to the profile of lean subjects than to the pattern of obese subjects before VLCD. Weight loss improves the inflammatory profile of obese subjects through a decrease of proinflammatory factors and an increase of anti-inflammatory molecules. The genes are expressed mostly in the stromavascular fraction of adipose tissue, which is shown to contain numerous macrophages. The beneficial effect of weight loss on obesity-related complications may be associated with the modification of the inflammatory profile in adipose tissue.

MeSH Terms
Adipose Tissue/metabolism Adult Caloric Restriction Female Gene Expression Profiling Gene Expression Regulation Humans Inflammation/genetics,metabolism Inflammation Mediators/metabolism Interleukin 1 Receptor Antagonist Protein Interleukin-10/biosynthesis,genetics Obesity/diet therapy,genetics,immunology Sialoglycoproteins/biosynthesis,genetics Weight Loss/genetics,physiology
Chemicals
IL1RN protein, human Inflammation Mediators Interleukin 1 Receptor Antagonist Protein Sialoglycoproteins Interleukin-10
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Clément Karine
INSERM Avenir Paris 6 University, EA 3502, Nutrition Department, AP/HP, Hôtel-Dieu, Paris, France. [email protected].
Viguerie Nathalie
Poitou Christine
Carette Claire
Pelloux Véronique
Curat Cyrile A
Sicard Audrey
Rome Sophie
Benis Arriel
Zucker Jean-Daniel
Vidal Hubert
Laville Martine
Barsh Gregory S
Basdevant Arnaud
Stich Vladimir
Cancello Raffaella
Langin Dominique
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
1530-6860
Published
2004-11-00
Pages
1657-69
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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