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Adenovirus E3-6.7K Maintains Calcium Homeostasis and Prevents Apoptosis and Arachidonic Acid Release

机译:腺病毒E3-6.7K维持钙稳态并防止细胞凋亡和花生四烯酸释放

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摘要

E3-6.7K is a small and hydrophobic membrane glycoprotein encoded by the E3 region of subgroup C adenovirus. Recently, E3-6.7K has been shown to be required for the downregulation of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) receptors by the adenovirus E3/10.4K and E3/14.5K complex of proteins. We demonstrate here that E3-6.7K has additional protective roles, independent of other virus proteins. In transfected Jurkat T-cell lymphoma cells, E3-6.7K was found to maintain endoplasmic reticulum-Ca2+ homeostasis and inhibit the induction of apoptosis by thapsigargin. The presence of E3-6.7K also lead to a reduction in the TNF-induced release of arachidonic acid from transfected U937 human histiocytic lymphoma cells. In addition, E3-6.7K protected cells against apoptosis induced through Fas, TNF receptor, and TRAIL receptors. Therefore, E3-6.7K confers a wide range of protective effects against both Ca2+ flux-induced and death receptor-mediated apoptosis.
机译:E3-6.7K是一种小的疏水膜糖蛋白,由C亚型腺病毒E3区编码。最近,已经证明,腺病毒E3 / 10.4K和E3 / 14.5K蛋白复合体下调肿瘤坏死因子(TNF)相关的凋亡诱导配体(TRAIL)受体需要E3-6.7K。我们在这里证明,E3-6.7K具有独立于其他病毒蛋白的附加保护作用。在转染的Jurkat T细胞淋巴瘤细胞中,发现E3-6.7K维持内质网Ca 2 + 稳态,并抑制毒胡萝卜素诱导细胞凋亡。 E3-6.7K的存在还导致TNF诱导的花生四烯酸从转染的U937人组织细胞淋巴瘤细胞中释放减少。此外,E3-6.7K保护细胞免受Fas,TNF受体和TRAIL受体诱导的细胞凋亡。因此,E3-6.7K对Ca 2 + 通量诱导的和死亡受体介导的细胞凋亡均具有广泛的保护作用。

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