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首页> 外文期刊>Journal of diabetes research. >Free Fatty Acids Activate Renin-Angiotensin System in 3T3-L1 Adipocytes through Nuclear Factor-kappa B Pathway
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Free Fatty Acids Activate Renin-Angiotensin System in 3T3-L1 Adipocytes through Nuclear Factor-kappa B Pathway

机译:游离脂肪酸通过核因子-κB途径激活3T3-L1脂肪细胞中的肾素-血管紧张素系统

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The activity of a local renin-angiotensin system (RAS) in the adipose tissue is closely associated with obesity-related diseases. However, the mechanism of RAS activation in adipose tissue is still unknown. In the current study, we found that palmitic acid (PA), one kind of free fatty acid, induced the activity of RAS in 3T3-L1 adipocytes. In the presence of fetuin A (Fet A), PA upregulated the expression of angiotensinogen (AGT) and angiotensin type 1 receptor (AT1R) and stimulated the secretion of angiotensin II (ANG II) in 3T3-L1 adipocytes. Moreover, the activation of RAS in 3T3-L1 adipocytes was blocked when we blocked Toll-like receptor 4 (TLR4) signaling pathway using TAK242 or NF-κB signaling pathway using BAY117082. Together, our results have identified critical molecular mechanisms linking PA/TLR4/NF-κB signaling pathway to the activity of the local renin-angiotensin system in adipose tissue.
机译:脂肪组织中局部肾素-血管紧张素系统(RAS)的活动与肥胖相关疾病密切相关。然而,在脂肪组织中RAS活化的机制仍是未知的。在当前的研究中,我们发现一种游离脂肪酸棕榈酸(PA)诱导3T3-L1脂肪细胞中RAS的活性。在胎球蛋白A(Fet A)存在的情况下,PA上调了3T3-L1脂肪细胞中血管紧张素原(AGT)和血管紧张素1型受体(AT1R)的表达,并刺激了血管紧张素II(ANG II)的分泌。此外,当我们使用TAK242阻断Toll样受体4(TLR4)信号途径或使用BAY117082阻断NF-κB信号途径时,阻断了3T3-L1脂肪细胞中RAS的激活。在一起,我们的结果已经确定了关键的分子机制,将PA / TLR4 /NF-κB信号传导途径与脂肪组织中局部肾素-血管紧张素系统的活性联系起来。

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