Arcidiacono Biagio, Chiefari Eusebio, Laria Anna Elisa, Messineo Sebastiano, Bilotta Francesco Luciano, Britti Domenico, Foti Daniela Patrizia, Foryst-Ludwig Anna, Kintscher Ulrich, Brunetti Antonio
Department of Health Sciences, University "Magna Græcia" of Catanzaro, 88100 Catanzaro, Italy.
Institute of Pharmacology, Center for Cardiovascular Research, 10117 Berlin, Germany.
World J Diabetes. 2017 Sep 15;8(9):422-428. doi: 10.4239/wjd.v8.i9.422.
To investigate matrix metalloproteinase-11 () expression in adipose tissue dysfunction, using and models of insulin resistance.
Culture of mouse 3T3-L1 preadipocytes were induced to differentiation into mature 3T3-L1 adipocytes. Cellular insulin resistance was induced by treating differentiated cultured adipocytes with hypoxia and/or tumor necrosis factor (TNF)-α, and transcriptional changes were analyzed in each condition thereafter. For the studies, expression levels were measured in white adipose tissue (WAT) from C57BL/6J mice that underwent low fat diet or high-fat feeding in order to induce obesity and obesity-related insulin resistance. Statistical analysis was carried out with GraphPad Prism Software.
mRNA expression levels were significantly higher in insulin resistant 3T3-L1 adipocytes compared to control cells (1.46 ± 0.49 0.83 ± 0.21, respectively; < 0.00036). The increase in expression was observed even in the presence of TNF-α alone (3.79 ± 1.11 1 ± 0.17, < 0.01) or hypoxia alone (1.79 ± 0.7 0.88 ± 0.1, < 0.00023). The results obtained in experiments were confirmed in the model of insulin resistance. In particular, mRNA was upregulated in WAT from obese mice compared to lean mice (5.5 ± 2.8 1.1 ± 0.7, respectively; < 3.72E-08). The increase in levels in obese mice was accompanied by the increase in typical markers of fibrosis, such as collagen type VI alpha 3 (), and fibroblast-specific protein 1.
Our results indicate that dysregulation of expression is an early process in the adipose tissue dysfunction, which leads to obesity and obesity-related insulin resistance.
利用胰岛素抵抗的细胞和动物模型,研究基质金属蛋白酶-11()在脂肪组织功能障碍中的表达情况。
将小鼠3T3-L1前脂肪细胞培养诱导分化为成熟的3T3-L1脂肪细胞。通过用缺氧和/或肿瘤坏死因子(TNF)-α处理分化后的培养脂肪细胞来诱导细胞胰岛素抵抗,然后分析每种条件下的转录变化。对于动物实验,测量低脂饮食或高脂喂养以诱导肥胖和肥胖相关胰岛素抵抗的C57BL/6J小鼠白色脂肪组织(WAT)中的表达水平。使用GraphPad Prism软件进行统计分析。
与对照细胞相比,胰岛素抵抗的3T3-L1脂肪细胞中的mRNA表达水平显著更高(分别为1.46±0.49对0.83±0.21;<0.00036)。即使仅存在TNF-α(3.79±1.11对1±0.17,<0.01)或仅存在缺氧(1.79±0.7对0.88±0.1,<0.00023)时,也观察到表达增加。在胰岛素抵抗的动物模型中证实了细胞实验获得的结果。特别是,与瘦小鼠相比,肥胖小鼠WAT中的mRNA上调(分别为5.5±2.8对1.1±0.7;<3.72E-08)。肥胖小鼠中水平的增加伴随着纤维化典型标志物如VI型胶原α3()和成纤维细胞特异性蛋白1的增加。
我们的结果表明,表达失调是脂肪组织功能障碍的早期过程,其导致肥胖和肥胖相关的胰岛素抵抗。