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胰岛素减弱肿瘤坏死因子α诱导的血红素结合蛋白mRNA表达:胰岛素在大鼠H4IIE肝癌细胞中的抗炎作用。

Insulin attenuates TNFα-induced hemopexin mRNA: An anti-inflammatory action of insulin in rat H4IIE hepatoma cells.

作者信息

Franklin J Lee, Bennett William L, Messina Joseph L

机构信息

University of Alabama at Birmingham, Department of Pathology, Division of Molecular and Cellular Pathology, Birmingham, AL 35294, United States.

Yale University, Interventional Cardiology, New Haven, CT 06510, United States.

出版信息

Biochem Biophys Rep. 2017 Jan 5;9:211-216. doi: 10.1016/j.bbrep.2016.12.013. eCollection 2017 Mar.

Abstract

Proinflammatory cytokines, including TNF-α and IL-6, can contribute to insulin resistance. Conversely, insulin has some actions that can be considered anti-inflammatory. Hemopexin is a Class 2 acute phase reactant and control of its transcription is predominantly regulated by IL-6, with TNF-α and IL-1β also inducing hemopexin gene expression. Thus, we asked whether insulin could inhibit the ability of TNF-α to stimulate hemopexin mRNA expression. In cultured rat hepatoma (H4IIE) cells, TNF-α significantly increased hemopexin mRNA accumulation. The TNF-α-induced increase of hemopexin mRNA was dramatically attenuated by insulin, even though TNF-α reduced peak insulin activation of ERK. Thus, even though TNF-α can contribute to insulin resistance, the residual insulin response was still able to counteract TNF-α actions.

摘要

包括肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)在内的促炎细胞因子可导致胰岛素抵抗。相反,胰岛素具有一些可被视为抗炎的作用。血红素结合蛋白是一种2类急性期反应物,其转录控制主要受IL-6调节,TNF-α和IL-1β也可诱导血红素结合蛋白基因表达。因此,我们研究了胰岛素是否能够抑制TNF-α刺激血红素结合蛋白mRNA表达的能力。在培养的大鼠肝癌(H4IIE)细胞中,TNF-α显著增加了血红素结合蛋白mRNA的积累。尽管TNF-α降低了细胞外信号调节激酶(ERK)的峰值胰岛素激活,但胰岛素显著减弱了TNF-α诱导的血红素结合蛋白mRNA增加。因此,尽管TNF-α可导致胰岛素抵抗,但残余的胰岛素反应仍能够抵消TNF-α的作用。

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