Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Biochemistry & Molecular Biology Regular Papers
Endogenous Prostaglandins E2 and F2α Serve as an Anti-Apoptotic Factor against Apoptosis Induced by Tumor Necrosis Factor-α in Mouse 3T3-L1 Preadipocytes
Kohji NISHIMURATsutomu SETOYAMAHirofumi TSUMAGARINana MIYATAYoko HATANOLi XUMitsuo JISAKATsutomu NAGAYAKazushige YOKOTA
Author information
JOURNAL FREE ACCESS

2006 Volume 70 Issue 9 Pages 2145-2153

Details
Abstract

Adipocytes can function as endocrine cells secreting a variety of adipocytokines including tumor necrosis factor (TNF)-α. Treatment of cultured mouse 3T3-L1 preadipocytes with TNF-α induced apoptosis, as was evident from increases in nuclear condensation and caspase-3 activity, but differentiated adipocytes during the maturation phase showed resistance to apoptosis by TNF-α. Antioxidants effectively reduced TNF-α-induced apoptosis in preadipocytes, indicating the involvement of reactive oxygen species. Exposure of preadipocytes to calcium ionophore A23187 reduced TNF-α-induced apoptosis, which was accompanied by increased production of prostaglandins (PGs) E2 and PGF2α. TNF-α preferentially promoted gene expression of cyclooxygenase (COX)-2 without affecting that of COX-1. Consistently, NS-398, a COX-2 inhibitor, stimulated TNF-α-induced apoptosis, which was reversed by exogenous PGE2 and PGF2α. These results indicate that endogenous PGE2 and PGF2α synthesized by preadipocytes through the induction of COX-2 can serve as anti-apoptotic factors against apoptosis by TNF-α.

Content from these authors

This article cannot obtain the latest cited-by information.

© 2006 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
Previous article Next article
feedback
Top