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7,8-二氢新蝶呤在体外T细胞凋亡及人嗜T淋巴细胞病毒1型转录中的作用

Role of 7,8-dihydroneopterin in T-cell apoptosis and HTLV-1 transcription in vitro.

作者信息

Baier-Bitterlich G, Baier G, Fuchs D, Böck G, Hausen A, Utermann G, Pavelka M, Wachter H

机构信息

Institute for Medical Chemistry and Biochemistry, University of Innsbruck, Austria.

出版信息

Oncogene. 1996 Nov 21;13(10):2281-5.

PMID:8950996
Abstract

Adult T-cell leukemia is associated with high levels of neopterin, released in large amounts from human macrophages upon stimulation with interferon-gamma. Recent data suggested a potential role of neopterin-derivatives in oxygen radical-mediated processes, and evidence accumulates that oxidative stress is involved in the pathogenesis of viral diseases. We now report that increased concentrations of 7,8-dihydroneopterin may lead to enhanced apoptosis and disturbance of the redox-balance of human leukemic Jurkat T cells. Additionally, we demonstrate that 7,8-dihydroneopterin and hydrogen peroxide activate the type 1 human T-cell leukemia virus (HTLV-1) long terminal repeat (LTR). Furthermore, we found that the activity of the HTLV-1 transactivator protein Tax is amplified by an elevated concentration of 7,8-dihydroneopterin. Tax did not significantly augment 7,8-dihydroneopterin mediated apoptosis. Based on our data we propose that 7,8-dihydroneopterin may be involved in the progression to higher stages of HTLV-1 associated disease.

摘要

成人T细胞白血病与新蝶呤水平升高有关,新蝶呤在人巨噬细胞受到γ干扰素刺激后大量释放。最近的数据表明新蝶呤衍生物在氧自由基介导的过程中可能发挥作用,并且越来越多的证据表明氧化应激参与了病毒性疾病的发病机制。我们现在报告,7,8-二氢新蝶呤浓度的增加可能导致人白血病Jurkat T细胞的凋亡增强和氧化还原平衡紊乱。此外,我们证明7,8-二氢新蝶呤和过氧化氢可激活1型人T细胞白血病病毒(HTLV-1)长末端重复序列(LTR)。此外,我们发现7,8-二氢新蝶呤浓度升高可增强HTLV-1反式激活蛋白Tax的活性。Tax并未显著增强7,8-二氢新蝶呤介导的凋亡。基于我们的数据,我们提出7,8-二氢新蝶呤可能参与HTLV-1相关疾病进展至更高阶段。

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