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干扰素-α抑制核转录因子NF-κB和活化蛋白1的激活,并增强肿瘤坏死因子诱导的细胞凋亡。

IFN-alpha suppresses activation of nuclear transcription factors NF-kappa B and activator protein 1 and potentiates TNF-induced apoptosis.

作者信息

Manna S K, Mukhopadhyay A, Aggarwal B B

机构信息

Cytokine Research Laboratory, Department of Bioimmunotherapy, MD Anderson Cancer Center, University of Texas, Houston, TX 77030, USA.

出版信息

J Immunol. 2000 Nov 1;165(9):4927-34. doi: 10.4049/jimmunol.165.9.4927.

Abstract

We and others have reported that IFN-alpha potentiates the apoptotic effects of TNF through a mechanism that is not understood. Because the nuclear transcription factors NF-kappaB and AP-1 have recently been reported to mediate anti-apoptosis and cell survival, we hypothesized that IFN-alpha potentiates the cytotoxic effects of TNF by suppressing TNF-induced activation of NF-kappaB and AP-1. We tested this hypothesis by pretreating human Jurkat T cells with IFN-alpha, which blocked TNF-induced activation of NF-kappaB and AP-1 in a time- and dose-dependent manner as determined by EMSA. IFN-alpha blocked TNF-induced phosphorylation and degradation of the inhibitor subunit of NF-kappaB, and suppressed NF-kappaB and AP-1 activation induced by various other inflammatory stimuli. NF-kappaB-dependent reporter gene expression activated by TNF, TNFR1, TNF receptor-associated factor 2, and NF-kappaB-inducing kinase was also abrogated by IFN-alpha pretreatment. The suppression of NF-kappaB and AP-1 correlated with the potentiation of TNF-induced cytotoxicity and caspase activation. Overall our results suggest that IFN-alpha potentiates the apoptotic effects of TNF possibly by suppressing NF-kappaB and AP-1 activation.

摘要

我们和其他研究人员曾报道,干扰素-α(IFN-α)可通过一种尚不明确的机制增强肿瘤坏死因子(TNF)的凋亡作用。由于近期有报道称核转录因子核因子κB(NF-κB)和活化蛋白-1(AP-1)介导抗凋亡和细胞存活,我们推测IFN-α通过抑制TNF诱导的NF-κB和AP-1活化来增强TNF的细胞毒性作用。我们通过用IFN-α预处理人Jurkat T细胞来验证这一假设,如通过电泳迁移率变动分析(EMSA)所确定的,IFN-α以时间和剂量依赖的方式阻断TNF诱导的NF-κB和AP-1活化。IFN-α阻断TNF诱导的NF-κB抑制亚基的磷酸化和降解,并抑制由各种其他炎症刺激诱导的NF-κB和AP-1活化。TNF、肿瘤坏死因子受体1(TNFR1)、肿瘤坏死因子受体相关因子2(TRAF2)和NF-κB诱导激酶激活的NF-κB依赖性报告基因表达也因IFN-α预处理而被消除。NF-κB和AP-1的抑制与TNF诱导的细胞毒性增强和半胱天冬酶激活相关。总体而言,我们的结果表明,IFN-α可能通过抑制NF-κB和AP-1活化来增强TNF的凋亡作用。

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