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Resistin up-regulates COX-2 expression via TAK1-IKK-NF-kappaB signaling pathway.

机译:抵抗素通过TAK1-IKK-NF-kappaB信号通路上调COX-2表达。

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摘要

The hormone resistin, which was originally shown to induce insulin resistance, has been implicated in the regulation of inflammatory processes, but the molecular mechanism underlying such regulation has not been clearly defined. The goal of our study was to determine whether the expression of COX-2 can be induced by resistin and what the potential signaling pathway involved in this process is. Compared with controls, resistin significantly upregulated COX-2 expression in RAW264.7 macrophage cells. Administration of anti-resistin antibody could significantly reduce this effect. Induction of COX-2 by resistin was also markedly reduced in the presence of either dominant negative mutant IkappaBalpha or PDTC, a pharmacological inhibitor of NF-kappaB. On the other hand, NF-kappaB subunit p65 was upregulated by resistin. Moreover, we found that transforming growth factor-beta-activated kinase 1 (TAK1), a mitogen-activated protein kinase kinase kinase (MAPKKK), could be activated in response to resistin. These results suggest that resistin enhances COX-2 expression in mouse macrophage cells in a TAK1-IKK-NF-kappaB-dependent manner and therefore plays a critical role in inflammatory processes.
机译:最初被证明可诱导胰岛素抵抗的激素抵抗素已与炎症过程的调节有关,但尚不清楚这种调节的分子机制。我们研究的目的是确定抵抗素是否可以诱导COX-2的表达以及该过程涉及的潜在信号途径是什么。与对照组相比,抵抗素显着上调了RAW264.7巨噬细胞中COX-2的表达。抗抵抗素抗体的给药可以显着降低这种作用。在显性负突变体IkappaBalpha或NF-kappaB的药理抑制剂PDTC的存在下,抵抗素对COX-2的诱导作用也显着降低。另一方面,NF-κB亚基p65被抵抗素上调。此外,我们发现转化生长因子-β激活的激酶1(TAK1),一种有丝分裂原激活的蛋白激酶激酶(MAPKKK),可以响应抵抗素而被激活。这些结果表明,抵抗素以TAK1-IKK-NF-κB依赖性方式增强了小鼠巨噬细胞中COX-2的表达,因此在炎症过程中起着至关重要的作用。

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