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Redox Modulation of the Apoptogenic Activity of Thapsigargin

机译:毒胡萝卜素凋亡活性的氧化还原调节。

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摘要

Thapsigargin (THG), a selective inhibitor of endoplasmic reticulum (ER) Ca~(2+)-ATPases, causes the rapid emptying of ER Ca~(2+); in some cell types, this is accompanied by apoptosis, whereas other cells maintain viability. In order to understand the molecular determinants of such a different behavior, we explored the role of oxygen versus nitrogen radicals, by analyzing the apoptogenic ability of THG in the presence of inhibitors of glutathione or nitric oxide (NO) synthesis, respectively. We observed that oxygen radicals play a sensitizing role whereas nitrogen radicals prevent THG-dependent apoptosis, showing that the apoptogenic effect of THG is redox sensitive.
机译:Thapsigargin(THG)是内质网(ER)Ca〜(2 +)-ATPases的选择性抑制剂,可导致ER Ca〜(2+)快速排空。在某些细胞类型中,这伴有凋亡,而其他细胞则保持活力。为了了解这种行为的分子决定因素,我们分别通过分析在谷胱甘肽或一氧化氮(NO)合成抑制剂存在下THG的凋亡能力,探讨了氧与氮自由基的作用。我们观察到氧自由基起增敏作用,而氮自由基阻止THG依赖性细胞凋亡,这表明THG的凋亡作用对氧化还原敏感。

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