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PMID: 17875176 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Obesity-induced inflammation: a metabolic dialogue in the language of inflammation.

Journal of internal medicine ·Vol. 262 ·No. 4 ·2007-10-00 ·Pages 408-14

Ferrante AW

Abstract

Obesity induces an inflammation state that is implicated in many clinically important complications, including insulin resistance, diabetes, atherosclerosis and non-alcoholic fatty liver disease. Although the cause and the molecular participants in this process remain incompletely defined, adipose tissue has a central role. Obesity-induced production of pro-inflammatory molecules, typified by TNF-alpha was recognized more than a dozen years ago, and since then more than two dozen other pro-inflammatory molecules induced by obesity have been identified. More recently a critical role for immune cells, specifically mononuclear phagocytes, in generating the obesity-induced inflammation has been identified. Defining the molecular and cellular components of obesity-induced inflammation offers the potential of identifying therapeutic targets that can ameliorate the complications associated with obesity.

MeSH Terms
Adipose Tissue/immunology Animals Cell Communication/physiology Diabetes Mellitus, Type 2/complications,immunology Humans Inflammation/complications,immunology,metabolism Insulin Resistance/physiology Macrophages/immunology Obesity/complications,immunology,metabolism Receptors, CCR2 Receptors, Chemokine/metabolism
Chemicals
CCR2 protein, human Receptors, CCR2 Receptors, Chemokine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Ferrante A W
Naomi Berrie Diabetes Center, Columbia University, New York, NY 10032, USA. awf7@columbia.edu
Article Info
Journal
Journal of internal medicine
Abbr.
J Intern Med
ISSN
0954-6820
Published
2007-10-00
Pages
408-14
Language
English
Region
England
NLM ID
8904841
Subset
IM
Grants
NIDDK NIH HHS · (DK066525 · United States
NIDDK NIH HHS · DK063608 · United States
NIDDK NIH HHS · DK59960 · United States
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