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人锰超氧化物歧化酶基因的核因子κB非依赖性转录诱导

NF kappa B-independent transcriptional induction of the human manganous superoxide dismutase gene.

作者信息

Borrello S, Demple B

机构信息

Department of Molecular and Cellular Toxicology, Harvard School of Public Health, Boston, Massachusetts 02165, USA.

出版信息

Arch Biochem Biophys. 1997 Dec 15;348(2):289-94. doi: 10.1006/abbi.1997.0355.

DOI:10.1006/abbi.1997.0355
PMID:9434740
Abstract

Numerous conditions induce expression of manganese-containing superoxide dismutase (MnSOD) in mammalian cells. The reported inducers of MnSOD are all agents that activate two transcription factors, AP-1 and NF kappa B, but several reports have suggested that MnSOD induction relies solely on NF kappa B. We investigated the contribution of the individual transcription factors by using antioxidants and metal chelators to modulate MnSOD transcriptional activation in response to phorbol esters or hydrogen peroxide. The results indicate substantial transcriptional induction of the MnSOD gene independent of NF kappa B. The metal chelator and antioxidant pyrrolidine dithiocarbamate (PDTC) at 60 or 100 microM induced the MnSOD transcript in HeLa cells while diminishing expression of the NF kappa B-responsive transcript I kappa B-alpha. Induction of the MnSOD mRNA by phorbol-12-myristate-13-acetate (PMA) was only slightly diminished in the presence of PDTC, which in contrast virtually eliminated induction of the NF kappa B-dependent transcript I kappa B-alpha by PMA. MnSOD RNA induction by H2O2 was only approximately 1.5-fold, compared to a ca. 3-fold activation of I kappa B-alpha expression. Two other antioxidants, N-acetyl-L-cysteine and butylated hydroxyanisole, failed to block induction of the MnSOD transcript by PMA, which is consistent with a role for AP-1. In vitro DNA binding studies confirmed strong AP-1 activation under conditions where NF kappa B is blocked but the MnSOD transcript is strongly induced (e.g., PMA treatment in the presence of PDTC).

摘要

许多情况可诱导哺乳动物细胞中含锰超氧化物歧化酶(MnSOD)的表达。已报道的MnSOD诱导剂均为能激活两种转录因子AP-1和核因子κB(NFκB)的物质,但有几份报告表明MnSOD的诱导仅依赖于NFκB。我们通过使用抗氧化剂和金属螯合剂来调节MnSOD的转录激活,以响应佛波酯或过氧化氢,从而研究单个转录因子的作用。结果表明MnSOD基因存在大量独立于NFκB的转录诱导。60或100μM的金属螯合剂及抗氧化剂吡咯烷二硫代氨基甲酸盐(PDTC)可诱导HeLa细胞中的MnSOD转录本,同时减少NFκB反应性转录本IκB-α的表达。在存在PDTC的情况下,佛波醇-12-肉豆蔻酸酯-13-乙酸酯(PMA)对MnSOD mRNA的诱导仅略有减少,相比之下,PMA对NFκB依赖性转录本IκB-α的诱导几乎完全被消除。与IκB-α表达约3倍的激活相比,H2O2对MnSOD RNA的诱导仅约为1.5倍。另外两种抗氧化剂N-乙酰-L-半胱氨酸和丁基羟基茴香醚未能阻断PMA对MnSOD转录本的诱导,这与AP-1的作用一致。体外DNA结合研究证实,在NFκB被阻断但MnSOD转录本被强烈诱导的条件下(例如在存在PDTC的情况下进行PMA处理),AP-1有强烈激活。

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