Kralisch Susan, Klein Johannes, Lossner Ulrike, Bluher Matthias, Paschke Ralf, Stumvoll Michael, Fasshauer Mathias
University of Leipzig, Department of Internal Medicine III, Ph.-Rosenthal-Str. 27, 04103 Leipzig, Germany.
FEBS Lett. 2005 Nov 21;579(28):6417-22. doi: 10.1016/j.febslet.2005.10.033. Epub 2005 Nov 2.
Tissue inhibitor of metalloproteinase (TIMP)-1 is an adipocyte-secreted protein upregulated in obesity which promotes adipose tissue development. Furthermore, the proinflammatory adipocytokines tumor necrosis factor alpha (TNFalpha) and interleukin (IL)-6 induce insulin resistance, and plasma concentrations are increased during weight gain. In the current study, the impact of TNFalpha and IL-6 on TIMP-1 mRNA and protein expression was determined in 3T3-L1 adipocytes. Interestingly, TNFalpha and IL-6 induced TIMP-1 protein secretion more than 3- and 2-fold, respectively. Furthermore, TIMP-1 mRNA was upregulated in a time- and dose-dependent fashion. Inhibitor experiments suggested that nuclear factor kappaB and p 44/42 mitogen-activated protein kinase are involved in both, basal and adipocytokine-induced TIMP-1 expression. Moreover, the thiazolidinedione troglitazone partly reversed TNFalpha- but not IL-6-induced TIMP-1 synthesis. Taken together, we demonstrate that TIMP-1 expression is selectively upregulated in fat cells by proinflammatory adipocytokines and might play a role in maintaining adipose tissue mass in obesity.
金属蛋白酶组织抑制剂(TIMP)-1是一种由脂肪细胞分泌的蛋白质,在肥胖状态下上调,可促进脂肪组织发育。此外,促炎脂肪细胞因子肿瘤坏死因子α(TNFα)和白细胞介素(IL)-6可诱导胰岛素抵抗,且体重增加期间血浆浓度会升高。在本研究中,我们测定了TNFα和IL-6对3T3-L1脂肪细胞中TIMP-1 mRNA和蛋白表达的影响。有趣的是,TNFα和IL-6分别使TIMP-1蛋白分泌增加了3倍多和2倍多。此外,TIMP-1 mRNA以时间和剂量依赖性方式上调。抑制剂实验表明,核因子κB和p44/42丝裂原活化蛋白激酶参与基础和脂肪细胞因子诱导的TIMP-1表达。此外,噻唑烷二酮类药物曲格列酮可部分逆转TNFα诱导的而非IL-6诱导的TIMP-1合成。综上所述,我们证明促炎脂肪细胞因子可选择性上调脂肪细胞中TIMP-1的表达,且可能在肥胖状态下维持脂肪组织量中发挥作用。