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In vitro studies on radiation induced membrane oxidative damage in apoptotic death of mouse thymocytes

机译:辐射诱导的小鼠胸腺细胞凋亡中膜氧化损伤的体外研究

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Radiation oxidative damage to the plasma membrane of cells and its consequences in the mechanism of apoptotic death have been receiving growing attention of radiation scientists in recent years. We have employed a fluorescence probe method to determine changes in the permeability and fluidity of the plasma membrane of mouse thymocytes following y irradiation within a low to moderate radiation dose range (a few cGy to 10 Gy; 0.71 Gy/min), In vitro studies have shown that radiation induced membrane changes were correlated with the induction of apoptotic cell death. Studies have also been carried out to evaluate the generation of intracellular reactive oxygen species (ROS) in response to radio-oxidative damage to thymocytes using a cytosolic fluorescence probe, 2'-7'-dichlorodihydrofluorescien diacetate (DCH-FDA). The apoptosis of the thymocytes was determined by measuring nuclear condensation using propidium iodide (PI) and DNA fragmentation by gel electrophoresis. The viability of the thymocytes was determined by the trypan blue exclusion method which was found to gradually decrease after incubation of irradiated cells for 7 h. Thymocytes labeled with DCH-FDA in PBS at 25℃ showed remarkably increased fluorescence intensity, measured after 30 min of irradiation (10 Gy), indicating an enhanced formation of intracellular reactive oxygen species. The DCH-FDA probe was able to sensitively detect irradiation effects on cells at lower doses (~20 cGy). The population of thymocytes with reduced nuclear diameter was found to progressively increase with the post-irradiation incubation time, following exposure to a particular radiation dose. Moreover, fragmentation of nuclear DNA in irradiated thymocytes, as observed by the pattern of ladder formation on agarose gel, was found to significantly increase on incubations beyond 3 h at 37℃. Results indicate that the enhanced amount of intracellular reactive oxygen species generated in response to radio-oxidative stress were linked with the induction of γ irradiation of apoptotic death in thymocytes. These observations and a highlight of emerging scenario in the area of low dose radiation effects at cellular and membrane levels are described.
机译:近年来,辐射氧化对细胞质膜的损害及其对凋亡死亡机制的影响已引起辐射科学家越来越多的关注。在体外研究中,我们采用荧光探针法确定了在低至中等辐射剂量范围(几cGy至10 Gy; 0.71 Gy / min)中y辐射后小鼠胸腺细胞质膜通透性和流动性的变化。已经表明,辐射诱导的膜变化与凋亡细胞死亡的诱导相关。还已经进行了研究以使用胞质荧光探针2'-7'-dichlorodihydrofluorescien diacetate(DCH-FDA)评估对胸腺细胞的放射氧化损伤而产生的细胞内活性氧(ROS)的产生。通过使用碘化丙啶(PI)测量核浓缩和通过凝胶电泳的DNA片段化来确定胸腺细胞的凋亡。通过锥虫蓝排除法测定胸腺细胞的活力,发现在将受辐照的细胞孵育7小时后其逐渐降低。在辐照30分钟(10 Gy)后测得,在25℃PBS中用DCH-FDA标记的胸腺细胞显示出显着增强的荧光强度,表明细胞内活性氧物种形成增加。 DCH-FDA探针能够以较低的剂量(〜20 cGy)灵敏地检测出对细胞的照射效果。发现暴露于特定的辐射剂量后,随着辐射后孵育时间的增加,核直径减小的胸腺细胞数量会逐渐增加。此外,通过在琼脂糖凝胶上形成梯形图,可以观察到辐射胸腺细胞中核DNA的断裂,在37℃下孵育3小时以上会明显增加。结果表明,响应于放射氧化应激而产生的细胞内活性氧种类的增加与诱导胸腺细胞凋亡死亡的γ辐射有关。描述了这些观察结果以及在细胞和膜水平的低剂量辐射效应领域中新兴场景的亮点。

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