Cheng Jie, Tang Liling, Xiao Deyou, Jiang Fangyi, Wang Jianfei, Mi Yan, Yao Chenguo, Sun Caixin
Key Laboratory of Biorheological Science and Technology, Ministry of Education, Bioengineering College, Chongqing University, Chongqing 400044, China.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2011 Jun;28(3):446-50.
In order to investigate the effects of electric pulses on cancer cells, we carried out the experiments with exposing HepG2 and L02 to electric pulses (1 kV/cm, l00 micros, 1 Hz) for different lengths of time (8 s, 15 s, 30 s, 60 s). Annexin V-FITC Kit and Flow cytometry were used to study the apoptosis of treated cells. The results showed that the electric pulses of 1 kV/cm, l00 micros, 1 Hz for 8 s could not induce tumor cells apoptosis. Apoptosis was observed when tumor cells were stimulated for 15 s and longer, and the apoptosis percentage increased with the increase of stimulation time. Furthermore, tumor cells were more sensitive than normal cells in response to electrical pulses. Rhodamine 123 and Laser Scanning Confocal Microscope (LSCM) were used to make a real-time study of mitochondrial transmembrane potential (Deltapsim) when the tumor cells were exposed to electric pulses for 60 s. No significant change of Deltapsim was observed within 30 s stimulation. After that, the Deltapsim increased sharply and declined later, suggesting that the mitochondrial pathway may be one of the apoptosis mechanism induced by electric pulses.
为了研究电脉冲对癌细胞的影响,我们进行了将HepG2和L02细胞暴露于电脉冲(1 kV/cm,100微秒,1 Hz)不同时长(8秒、15秒、30秒、60秒)的实验。使用膜联蛋白V-异硫氰酸荧光素(Annexin V-FITC)试剂盒和流式细胞术研究处理后细胞的凋亡情况。结果表明,1 kV/cm、100微秒、1 Hz的电脉冲作用8秒不能诱导肿瘤细胞凋亡。当肿瘤细胞受到15秒及更长时间的刺激时可观察到凋亡,且凋亡百分比随刺激时间的增加而升高。此外,肿瘤细胞对电脉冲的反应比正常细胞更敏感。当肿瘤细胞暴露于电脉冲60秒时,使用罗丹明123和激光扫描共聚焦显微镜(LSCM)对线粒体跨膜电位(Δψm)进行实时研究。在30秒刺激内未观察到Δψm有明显变化。此后,Δψm急剧升高,随后下降,这表明线粒体途径可能是电脉冲诱导凋亡的机制之一。