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首页> 外文期刊>International journal of hyperthermia: The official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group >Apoptotic and necrotic effects of tumour necrosis factor-alpha potentiated with hyperthermia on L929 and tumour necrosis factor-alpha-resistant L929.
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Apoptotic and necrotic effects of tumour necrosis factor-alpha potentiated with hyperthermia on L929 and tumour necrosis factor-alpha-resistant L929.

机译:热疗增强的肿瘤坏死因子-α对L929和耐肿瘤坏死因子-α的L929的凋亡和坏死作用。

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PURPOSE: The cytotoxic effect of the combination treatment of TNF-alpha and hyperthermia on L929 and TNF-alpha-resistant L929 (rL929) cells was investigated. MATERIALS AND METHODS: L929 cells were treated with TNF-alpha (5 ng/mL), heating at 43 degrees C or the combination of TNF-alpha and heating. The cells were harvested at different time within the 24-hour period. The viability and the type of cell death of the harvested cells were examined. RESULTS: When L929 cells were treated with a combination of TNF-alpha and heating the cells died quickly and apoptosis increased to an overwhelming extent, especially in the group pre-treated with TNF-alpha for 1 h prior to heating. Although rL929 cells were resistant to TNF-alpha alone, the cells became sensitive to TNF-alpha treatment when combined with heating. Similar to the L929 cell, the cells also died rapidly and exhibited apoptosis to a higher extent. Using an Annexin-V-FITC kit and flow cytometer, we found that both necrosis and apoptosis occurred. Agarose gel electrophoresis of DNA extracted from treated cells showed that the DNA fragments were multiples of approximately 200 bp. Furthermore, by studying the kinetics of cell death and apoptosis, we found that the loss of cell membrane integrity preceded the DNA fragmentation in both L929 and rL929 cells. CONCLUSION: The results suggested that hyperthermia may enhance the necrotic and apoptotic effects of TNF-alpha on some tumour cells and overcome the resistance of some tumour cells to TNF-alpha.
机译:目的:研究TNF-α和热疗联合治疗对L929和耐TNF-α的L929(rL929)细胞的细胞毒性作用。材料与方法:L929细胞用TNF-α(5 ng / mL),43摄氏度加热或TNF-α加热结合处理。在24小时内的不同时间收获细胞。检查了所收获细胞的活力和细胞死亡类型。结果:当用TNF-α组合治疗L929细胞并加热时,细胞迅速死亡,凋亡增加到了压倒性的程度,尤其是在加热前用TNF-α预处理1 h的组。尽管rL929细胞仅对TNF-α有抗性,但结合加热后,细胞对TNF-α处理变得敏感。与L929细胞相似,这些细胞也迅速死亡并且表现出更高程度的细胞凋亡。使用膜联蛋白-V-FITC试剂盒和流式细胞仪,我们发现坏死和凋亡均发生。从处理过的细胞中提取的DNA的琼脂糖凝胶电泳显示,DNA片段约为200 bp的倍数。此外,通过研究细胞死亡和凋亡的动力学,我们发现细胞膜完整性的丧失先于L929和rL929细胞的DNA断裂。结论:热疗可以增强TNF-α对某些肿瘤细胞的坏死和凋亡作用,并克服某些肿瘤细胞对TNF-α的抗性。

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