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The mAb against adipocyte fatty acid-binding protein 2E4 attenuates the inflammation in the mouse model of high-fat diet-induced obesity via toll-like receptor 4 pathway

机译:抗脂肪细胞脂肪酸结合蛋白2E4通过Toll样受体4途径衰减高脂饮食诱导的肥胖症小鼠模型中的炎症

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Adipocyte fatty acid-binding protein (A-FABP) plays an important role in fatty acid-mediated processes and related metabolic and inflammatory responses. In this study, we prepared a novel monoclonal antibody against A-FABP, designated 2E4. Our data showed that 2E4 specifically binded to the recombinant A-FABP and native A-FABP of mice adipose tissue. Furthermore, we investigated the effect of 2E4 on metabolic and inflammatory responses in C57BL/6J obese mice fed on a high fat diet. 2E4 administration improved glucose response in high-fat-diet induced obese mice. The 2E4 treated groups exhibited lower free fatty acids, cholesterol, and triglycerides in a concentration-dependent manner. These changes were accompanied by down-regulated expression of pro-inflammatory cytokines in adipose tissue, including tumor necrosis factor alpha, monocyte chemotactic protein-1, and interleukin-6. Meanwhile, our data demonstrated that 2E4 significantly decreased the mRNA and protein levels of A-FABP in adipose tissue of mice. Further experiments showed that 2E4 notably suppressed the phosphorylation of I kappa B alpha and jun-N-terminal kinase through toll-like receptor 4 signaling pathway. Taken together, 2E4 is an effective monoclonal antibody against A-FABP, which attenuated the inflammatory responses induced in the high-fat-diet mice. These findings may provide scientific insight into the treatment of chronic low-grade inflammation in obesity. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:脂肪细胞脂肪酸结合蛋白(A-FABP)在脂肪酸介导的方法和相关代谢和炎症反应中起重要作用。在这项研究中,我们制备了针对A-Fabp的新型单克隆抗体,指定为2E4。我们的数据表明,2E4特异性结合重组A-FABP和小鼠的天然A-FABP脂肪组织。此外,我们研究了2E4对高脂饮食中C57BL / 6J肥胖小鼠的代谢和炎症反应的影响。 2E4给药改善高脂饮食诱导的肥胖小鼠的葡萄糖反应。 2E4处理基团以浓度依赖性方式表现出低级游离脂肪酸,胆固醇和甘油三酯。这些变化伴随着脂肪组织中的促炎细胞因子的下调表达,包括肿瘤坏死因子α,单核细胞趋化蛋白-1和白细胞介素-6。同时,我们的数据表明,2E4显着降低小鼠脂肪组织中A-Fabp的mRNA和蛋白质水平。进一步的实验表明,通过Toll样受体4信号通路,2E4显着抑制IκBα和Jun-N-末端激酶的磷酸化。连合在一起,2E4是针对A-FABP的有效单克隆抗体,其减弱了高脂饮食小鼠中诱导的炎症反应。这些发现可以科学洞察肥胖症治疗慢性低级炎症。 (c)2014年Elsevier Ireland Ltd.保留所有权利。

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