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PMID: 17699733 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Thematic review series: Adipocyte Biology. Adipocyte stress: the endoplasmic reticulum and metabolic disease.

Journal of lipid research ·Vol. 48 ·No. 9 ·2007-09-00 ·Pages 1905-14

Gregor MF, Hotamisligil GS

Abstract

In the context of obesity and its related maladies, the adipocyte plays a central role in the balance, or imbalance, of metabolic homeostasis. An obese, hypertrophic adipocyte is challenged by many insults, including surplus energy, inflammation, insulin resistance, and considerable stress to various organelles. The endoplasmic reticulum (ER) is one such vital organelle that demonstrates significant signs of stress and dysfunction in obesity and insulin resistance. Under normal conditions, the ER must function in the unique and trying environment of the adipocyte, adapting to meet the demands of increased protein synthesis and secretion, energy storage in the form of triglyceride droplet formation, and nutrient sensing that are particular to the differentiated fat cell. When nutrients are in pathological excess, the ER is overwhelmed and the unfolded protein response (UPR) is activated. Remarkably, the consequences of UPR activation have been causally linked to the development of insulin resistance through a multitude of possible mechanisms, including c-jun N-terminal kinase activation, inflammation, and oxidative stress. This review will focus on the function of the ER under normal conditions in the adipocyte and the pathological effects of a stressed ER contributing to adipocyte dysfunction and a thwarted metabolic homeostasis.

MeSH Terms
Adipocytes/physiology Animals Cholesterol/metabolism Endoplasmic Reticulum/drug effects,physiology Humans Inflammation/physiopathology Lipid Metabolism/physiology Metabolic Diseases/physiopathology Obesity/physiopathology Phenylbutyrates/pharmacology Protein Folding Proteins/metabolism Stress, Physiological/physiopathology Taurochenodeoxycholic Acid/pharmacology
Chemicals
Phenylbutyrates Proteins Taurochenodeoxycholic Acid ursodoxicoltaurine 4-phenylbutyric acid Cholesterol
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gregor Margaret F
Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Hotamisligil Gökhan S
Article Info
Journal
Journal of lipid research
Abbr.
J Lipid Res
ISSN
0022-2275
Published
2007-09-00
Epub
2007-00-09
Pages
1905-14
Language
English
Region
United States
NLM ID
0376606
Subset
IM
Grants
NIDDK NIH HHS · T90 DK-070078 · United States
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