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汉坦病毒感染中死亡结构域相关蛋白 6(DAXX)介导的细胞凋亡被干扰素刺激的核转录因子的激活所抵消。

Death-domain associated protein-6 (DAXX) mediated apoptosis in hantavirus infection is counter-balanced by activation of interferon-stimulated nuclear transcription factors.

机构信息

Whittemore Peterson Institute, University of Nevada-Reno, Reno, USA.

出版信息

Virology. 2013 Sep 1;443(2):338-48. doi: 10.1016/j.virol.2013.05.024. Epub 2013 Jul 3.

Abstract

Hantaviruses are negative strand RNA species that replicate predominantly in the cytoplasm. They also activate numerous cellular responses, but their involvement in nuclear processes is yet to be established. Using human umbilical vein endothelial cells (HUVECs), this study investigates the molecular finger-print of nuclear transcription factors during hantavirus infection. The viral-replication-dependent activation of pro-myelocytic leukemia protein (PML) was followed by subsequent localization in nuclear bodies (NBs). PML was also found in close proximity to activated Sp100 nuclear antigen and interferon-stimulated gene 20 kDa protein (ISG-20), but co-localization with death-domain associated protein-6 (DAXX) was not observed. These data demonstrate that hantavirus triggers PML activation and localization in NBs in the absence of DAXX-PLM-NB co-localization. The results suggest that viral infection interferes with DAXX-mediated apoptosis, and expression of interferon-activated Sp100 and ISG-20 proteins may indicate intracellular intrinsic antiviral attempts.

摘要

汉坦病毒是负链 RNA 病毒,主要在细胞质中复制。它们还激活许多细胞反应,但它们在核过程中的参与尚未确定。本研究使用人脐静脉内皮细胞 (HUVEC) 研究汉坦病毒感染过程中核转录因子的分子指纹。病毒复制依赖性的早幼粒细胞白血病蛋白 (PML) 的激活,随后定位于核体 (NB)。还发现 PML 与活化的 Sp100 核抗原和干扰素刺激基因 20kDa 蛋白 (ISG-20) 密切相关,但未观察到与死亡结构域相关蛋白-6 (DAXX) 的共定位。这些数据表明,汉坦病毒在没有 DAXX-PLM-NB 共定位的情况下触发 PML 的激活和在 NB 中的定位。结果表明,病毒感染干扰了 DAXX 介导的细胞凋亡,干扰素激活的 Sp100 和 ISG-20 蛋白的表达可能表明细胞内固有抗病毒尝试。

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