An inflammatory micro-environment promotes human adipocyte apoptosis

被引:40
|
作者
Keuper, Michaela [1 ]
Blueher, Matthias [2 ]
Schoen, Michael R. [3 ]
Moeller, Peter [4 ]
Dzyakanchuk, Anna [5 ]
Amrein, Kurt [5 ]
Debatin, Klaus-Michael
Wabitsch, Martin [1 ]
Fischer-Posovszky, Pamela [1 ]
机构
[1] Univ Ulm, Diabet & Obes Unit, Div Pediat Endocrinol, Dept Pediat & Adolescent Med, D-89075 Ulm, Germany
[2] Univ Leipzig, Dept Med 3, Leipzig, Germany
[3] Stadt Klinikum Karlsruhe, Clin Visceral Surg, Karlsruhe, Germany
[4] Univ Ulm, Inst Pathol, D-89075 Ulm, Germany
[5] Hoffmann La Roche Ag, CH-4002 Basel, Switzerland
关键词
Inflammation; Fat cells; Macrophages; Apoptosis; Insulin resistance; MACROPHAGE-CONDITIONED MEDIUM; GROWTH-FACTOR-I; INSULIN-RESISTANCE; ADIPOSE-TISSUE; DEPENDENT MANNER; CELL-DEATH; OBESITY; FAT; HYPOXIA; KINASE;
D O I
10.1016/j.mce.2011.04.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Obesity-associated macrophage infiltration into adipose tissue is responsible for both local and systemic inflammation. Recent findings suggest fat cell apoptosis as an initiator of macrophage recruitment. Here, we investigated the effects of an inflammatory micro-environment on fat cells using human THP-1 macrophages and SGBS adipocytes. Macrophage-secreted factors induced insulin resistance, inhibited insulin-stimulated Akt phosphorylation, and induced apoptosis of adipocytes. The apoptosis-inducing effect was even more pronounced in direct co-cultures of adipocytes and macrophages. Our data suggest a link between insulin resistance and apoptosis sensitivity. Accordingly, pharmacological and genetic inhibition of insulin signaling at the level of Akt2 sensitized adipocytes to apoptosis induction by macrophage-secreted factors. In conclusion, we describe here a novel interaction of macrophages and fat cells, i.e. induction of apoptosis. Our data suggest a feed-forward cycle in which macrophages further drive the inflammatory process by inducing insulin resistance and concomitant apoptosis of adipocytes. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
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