Diabetes
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Diabetes Publish Ahead of Print published online ahead of print August 4, 2008
DOI: 10.2337/db08-0592

This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
db08-0592v1
57/11/2992    most recent
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Joy Espiritu, D.
Right arrow Articles by Mazzone, T.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Joy Espiritu, D.
Right arrow Articles by Mazzone, T.
Social Bookmarking
 Add to CiteULike   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Original Research

Oxidative stress regulates adipocyte apolipoprotein E and suppresses its expression in obesity

Doris Joy Espiritu1, and Theodore Mazzone2

1Department of Medicine
2Departments of Medicine, Pharmacology, and Human Nutrition, University of Illinois at Chicago, Chicago, Illinois 60612

Objective: Endogenous expression of apoE has a significant impact on adipocyte lipid metabolism and is markedly suppressed in obesity. Adipose tissue oxidant stress is emerging as an important mediator of adipocyte dysfunction. These studies were undertaken to evaluate the role of oxidant stress for regulation of adipocyte apoE.

Research Design and Methods: ApoE gene and protein expression in 3T3-L1 adipocytes, or mature adipocytes and adipose tissue from C57/Bl6 mice was evaluated after induction of oxidant stress. The response of adipose tissue and adipocytes from obese compared to lean mice to antioxidants was also assessed.

Results: Oxidant stress in 3T3-L1 cells, or adipocytes and adipose tissue from lean mice significantly reduced apoE mRNA and protein level. Inclusion of an antioxidant eliminated this reduction. Oxidant stress was accompanied by activation of the NF-{kappa}B transcription complex and its effect on apoE was eliminated by an NF-{kappa}B activation inhibitor. Treatment of freshly isolated adipose tissue or mature adipocytes from obese mice with antioxidant increased apoE expression but had no effect on cells or tissue from lean mice. Incubation of freshly isolated adipocytes from lean mice with stromovascular cells from obese mice significantly suppressed adipocyte apoE compared to incubation with stromovascular cells from lean mice, but this suppression was reversed by inclusion of antioxidant or a neutralizing antibody to TNF{alpha}.

Conclusions: Oxidant stress significantly modulates adipose tissue and adipocyte apoE expression. Further, oxidant stress contributes to suppression of adipocyte apoE in obesity. This suppression depends on interaction between adipose tissue stromovascular cells and adipocytes.


Correspondence: tmazzone{at}uic.edu

Key Words: adipose tissue inflammation • reactive oxygen species • apolipoproteins • adipocytes • obesity


Add to CiteULike CiteULike   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Diabetes Diabetes Care Clinical Diabetes Diabetes Spectrum
Copyright © 2008 by the American Diabetes Association.