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Interleukin-6 is a positive regulator of tumor necrosis factor α-induced adipose-related protein in 3T3-L1 adipocytes
被引:36
作者:
Fasshauer, M
Kralisch, S
Klier, M
Lossner, U
Bluher, M
Chambaut-Guérin, AM
Klein, J
Paschke, R
[1
]
机构:
[1] Univ Leipzig, Dept Internal Med 3, D-04103 Leipzig, Germany
[2] Univ Paris 06, CNRS, UMR 7079, Ctr Rech Biomed Cordeliers, F-75270 Paris 06, France
[3] Univ Lubeck, Dept Internal Med 1, D-23538 Lubeck, Germany
关键词:
adipocyte;
insulin resistance;
interleukin-6;
obesity;
tumor necrosis factor alpha;
tumor necrosis factor alpha-induced adipose-related protein;
D O I:
10.1016/S0014-5793(04)00096-1
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:
Tumor necrosis factor (TNF) alpha-induced adipose-related protein (TIARP) is a novel TNFalpha-stimulated protein in adipocytes. Besides TNFalpha, interleukin (IL)-6 has recently been shown to be another adipocytokine implicated in insulin resistance. Therefore, the impact of IL-6 on TIARP gene expression in 3T3-L1 adipocytes was determined by quantitative real-time reverse transcription-polymerase chain reaction. Interestingly, TIARP mRNA expression was stimulated up to 3.8-fold by IL-6 in a dose-dependent fashion with significant stimulation detectable at effector concentrations as low as 3 ng/ml and maximal effects seen at 100 ng/ml IL-6. Induction of TIARP mRNA by IL-6 was time-dependent with significant upregulation occurring as early as 2 h after effector addition and maximal effects observed at 4 h. In parallel, TIARP protein synthesis was upregulated with maximal effects seen after 8 h of IL-6 treatment. Furthermore, the Janus kinase 2 inhibitor AG490 decreased TIARP mRNA expression. The increase of TIARP mRNA could be reversed by withdrawal of IL-6 for 24 h, Furthermore, TIARP mRNA induction by IL-6 was also seen in brown adipocytes but not in muscle and liver cells. Taken together, these results show that TIARP is acutely regulated in adipose tissue not only by TNFalpha but also by IL-6 which has teen shown to be another important cytokine implicated in the pathogenesis of insulin resistance. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:153 / 157
页数:5
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