TNFα induces and insulin inhibits caspase 3-dependent adipocyte apoptosis

被引:53
作者
Qian, H
Hausman, DB
Compton, MM
Martin, RJ
Della-Fera, MA
Hartzell, DL
Baile, CA
机构
[1] Univ Georgia, Dept Foods & Nutr, Athens, GA 30602 USA
[2] Univ Georgia, Dept Poultry Sci, Athens, GA 30602 USA
关键词
tumor necrosis factor-alpha; insulin; adipocytes; apoptosis; caspase; 3;
D O I
10.1006/bbrc.2001.5100
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of fat cell number by apoptosis is proposed to be part of a normal physiological cycle in adipose growth and development. To investigate this process, cultured rat adipocytes were treated with various concentrations of tumor necrosis factor alpha (TNF alpha) and/or insulin to determine the roles of these factors in adipocyte apoptosis. The cells were analyzed by flow cytometry using a TUNEL assay. TNF alpha increased adipocyte apoptosis in a dose-dependent fashion. TNF alpha-mediated apoptosis was detectable within 6 h of treatment and continued to increase with time. Decreasing media insulin concentration from 8.5 to 0.85 nM resulted in increased adipocyte apoptosis, whereas high doses of insulin protected adipocytes from TNF alpha-induced apoptosis. TNF alpha-activated apoptosis was accompanied by an increase in caspase 3 activity and could be inhibited by a caspase S-specific inhibitor. These data suggest that adipose tissue cell number is regulated, in part, by an apoptotic signaling pathway that involves TNF alpha, insulin, and caspase 3. (C) 2001 Academic Press.
引用
收藏
页码:1176 / 1183
页数:8
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