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肌细胞增强因子2介导T淋巴细胞中白细胞介素-2基因的钙依赖性转录:一种与活化T细胞核因子(NFAT)不同但与之协作的钙信号传导模块。

Myocyte enhancer factor 2 mediates calcium-dependent transcription of the interleukin-2 gene in T lymphocytes: a calcium signaling module that is distinct from but collaborates with the nuclear factor of activated T cells (NFAT).

作者信息

Pan Fan, Ye Zhaohui, Cheng Linzhao, Liu Jun O

机构信息

Department of Pharmacology and Molecular Science and Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

J Biol Chem. 2004 Apr 9;279(15):14477-80. doi: 10.1074/jbc.C300487200. Epub 2004 Jan 13.

DOI:10.1074/jbc.C300487200
PMID:14722108
Abstract

The second messenger calcium plays an essential role in the T cell receptor-mediated signal transduction pathways leading to transcription of the interleukin-2 gene. A key mechanism of calcium signaling has been shown to be mediated by calcineurin and NFAT. We report herein that the transcription factor myocyte enhancer factor (MEF)-2 is another calcium signal transducer involved in the regulation of the interleukin (IL)-2 promoter. A MEF2-binding site was identified in proximity to the TATA box of the IL-2 promoter. This site was shown to be bound by MEF2 in both resting and activated T cells. Overexpression of MEF2 enhanced, while overexpression of a dominant negative form of MEF2 or the MEF2-specific transcriptional corepressors Cabin1 and histone deacetylase 4 inhibited, the T cell receptor-dependent activation of an IL-2 reporter gene. Down-regulation of MEF2 by RNA interference in primary human T cells led to the inhibition of endogenous IL-2 transcription. These results suggest that MEF2 is required for the transcriptional activation of IL-2 and likely other cytokine genes in response to calcium signaling and may serve as a novel target for development of immunosuppressants.

摘要

第二信使钙离子在导致白细胞介素-2基因转录的T细胞受体介导的信号转导途径中起着至关重要的作用。钙离子信号传导的一个关键机制已被证明是由钙调神经磷酸酶和活化T细胞核因子介导的。我们在此报告,转录因子肌细胞增强因子(MEF)-2是另一种参与白细胞介素(IL)-2启动子调控的钙离子信号转导分子。在IL-2启动子的TATA盒附近鉴定出一个MEF2结合位点。该位点在静息和活化的T细胞中均被证明能与MEF2结合。MEF2的过表达增强了IL-2报告基因的T细胞受体依赖性激活,而MEF2的显性负性形式或MEF2特异性转录共抑制因子Cabin1和组蛋白去乙酰化酶4的过表达则抑制了这种激活。在原代人T细胞中通过RNA干扰下调MEF2导致内源性IL-2转录受到抑制。这些结果表明,MEF2是IL-2以及可能其他细胞因子基因响应钙离子信号进行转录激活所必需的,并且可能成为开发免疫抑制剂的新靶点。

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