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首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >Differential changes in sphingolipids between TNF-induced necroptosis and apoptosis in U937 cells and necroptosis-resistant sublines
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Differential changes in sphingolipids between TNF-induced necroptosis and apoptosis in U937 cells and necroptosis-resistant sublines

机译:TNF诱导的坏死性硬化与U937细胞和坏死性硬化亚系凋亡之间的鞘脂差异性变化

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Differential changes in various sphingolipids between TNF-induced necroptosis and apoptosis were investigated using liquid chromatography-tandem mass spectrometry. A marked increase in d18:1/16:0 ceramide was detected in U937 cells treated with TNF in the presence of Z-VAD-fmk (VAD). The level of d18:1/16:0 ceramide in necroptosis was almost twice as high as that in apoptosis after 4h, while an increase in PI-positive cells was observed only in necroptosis within 4 h. Necroptosis-resistant U937 (UNR) sublines were established to more clearly discriminate between necroptosis and apoptosis. All three UNR sublines were almost completely resistant to the treatment with TNF/VAD, but were as sensitive to TNF-induced apoptosis as parental cells. The expression of RIP3, a pivotal kinase in necroptosis, was lost in all three UNR sublines. In contrast with the large increase in ceramide levels in TNF/VAD-treated parental cells, they were only slightly increased in UNR cells. Although intracellular levels of reactive oxygen species (ROS) were elevated in both necroptosis and apoptosis, the treatment with butylated hydroxyanisole, an antioxidant, significantly inhibited increases in ceramide levels and PI-positive cells only in necroptosis. These results implicate that the ROS-induced large increase in ceramide levels may play a role in plasma membrane permeabilization in TNF-induced necroptosis. (C) 2015 Elsevier Ltd. All rights reserved.
机译:使用液相色谱-串联质谱法研究了TNF诱导的坏死和细胞凋亡之间各种鞘脂的差异性变化。在Z-VAD-fmk(VAD)存在的情况下,在用TNF处理的U937细胞中检测到d18:1/16:0神经酰胺的显着增加。坏死性病变中d18:1/16:0的神经酰胺水平几乎是4h后凋亡的两倍,而仅在坏死性病变中4h内观察到PI阳性细胞的增加。建立了抗坏死病性U937(UNR)子系,以更清楚地区分坏死性病和细胞凋亡。这三个UNR亚型几乎都完全抵抗TNF / VAD的治疗,但对TNF诱导的凋亡与亲代细胞一样敏感。 RIP3(一种坏死性关键激酶)的表达在所有三个UNR亚系中均丢失。与在接受TNF / VAD处理的亲代细胞中神经酰胺水平大幅增加相反,在UNR细胞中它们仅略有增加。尽管在尸检和凋亡中细胞内活性氧(ROS)的水平均升高,但是仅在尸检中,使用丁基化羟基茴香醚(一种抗氧化剂)才能显着抑制神经酰胺水平和PI阳性细胞的升高。这些结果表明,ROS诱导的神经酰胺水平的大量增加可能在TNF诱导的坏死性细胞质膜透化中起作用。 (C)2015 Elsevier Ltd.保留所有权利。

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