陡脉冲电场对肝癌细胞生物流变学特性的影响
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
肿瘤是危害人类健康最严重的疾病之一,其侵袭转移过程存在着复杂的生物流变学问题。目前,肿瘤的治疗方法主要有化学治疗、放射治疗、生物治疗、电穿孔治疗及外科手术治疗等,其中电穿孔疗法是近年来发展起来的一种杀伤肿瘤组织/细胞的新技术,并逐渐成为癌症综合治疗的有效手段之一,但人们对于脉冲电场治疗肿瘤的机理至今尚缺乏全面的认识。
     本项目将生物流变学和电工理论新技术有机结合,采用陡脉冲电场在一定条件下作用肝癌细胞,首先考查陡脉冲电场作用后肝癌细胞生长、增殖、凋亡相关基因的表达变化及其相关规律,然后用微管吸吮技术在单个细胞水平上研究陡脉冲电场作用后肝癌细胞粘弹特性、与内皮细胞粘附特性的变化情况,从生物流变学的角度探索陡脉冲电场杀伤肿瘤细胞的机理。主要研究工作和结果如下:
     1.陡脉冲电场实验装置及刺激参数
     能量可控陡脉冲实验装置由重庆大学高电压及电工理论新技术教育部重点实验室自行研制,该仪器主要由直流高压产生电路、陡脉冲的形成与整形输出电路和计算机采集测量系统三部分组成。根据陡脉冲电场杀伤肿瘤细胞/组织的前期研究基础,本文选择固定脉冲峰值(200 V)、频率(100 Hz)及刺激时间(10min) 3个参数,改变电容值(取0.01μF和0.1μF高低两种刺激剂量)观察陡脉冲电场对肝癌细胞增殖和生物流变特性的影响。
     2.陡脉冲电场对肝癌细胞生长和增殖的影响
     采用MTT法分析了陡脉冲电场作用后肝癌细胞增殖的变化,流式细胞技术分析了细胞周期分布的变化。结果表明:陡脉冲电场对肝癌细胞生长和增殖有明显的抑制作用;高剂量的陡脉冲电场抑制程度更为明显。肝癌细胞经陡脉冲电场作用后,细胞周期分布发生改变,细胞G0/G1期增加,S期和G2/M期减少。提示陡脉冲电场刺激能阻止肝癌细胞进入S期。
     3.陡脉冲电场对肝癌细胞凋亡相关基因表达的影响
     采用流式细胞技术考察了陡脉冲电场作用后肝癌细胞bcl-2和p53基因表达的变化,结果表明:陡脉冲电场能下调肝癌细胞bcl-2基因的表达,但p53基因的表达不受陡脉冲电场的影响,提示陡脉冲电场诱导肝癌细胞凋亡,可能是通过降低bcl-2的表达实现的。
     4.陡脉冲电场对肝癌细胞粘弹性的影响
     与对照组比较,低剂量陡脉冲电场处理组的弹性系数K1没有明显变化,但高剂量处理组的弹性系数K1明显降低;低剂量处理组的弹性系数K2没有明显变化,但高剂量处理组的弹性系数K2明显升高;粘性系数μ在陡脉冲电场处理后都有所增高,但高剂量处理组比低剂量处理组增高的程度更大。陡脉冲电场处理后,各组细胞初始变形程度没有差别;但与对照组比较,高剂量处理组细胞的最大变形程度有所增高;陡脉冲电场作用后细胞蠕变时间增长,高剂量组增加的程度更明显。
     5.陡脉冲电场对肝癌细胞与内皮粘附力的影响
     与对照组比较,低剂量刺激组肝癌细胞与内皮细胞的粘附力明显降低,而高剂量刺激组的粘附力没有明显变化。
Malignant tumor is one of the most severe diseases which does harm to human’s health. At present, the main treatments for tumor include chemical therapy, radiation therapy, biologic therapy and electroporotion therapy. Electroporotion therapy is a new developed technique to kill malignant tissues or cells and has become one of the efficient methods of tumor comprehensive treatment. However there is lack of all-round understanding about the mechanisms of electroporotion therapy to tumor.
     In this thesis, we combined biorheology and electrical technique, and investigated the growth, proliferation and apoptosis related gene expression of hepatoma cells treated by EPEF. We also studied the change of viscoelasticity、adhesive force of hepatoma cells to human umbilical vein endothelial cells(HUVECs) using of micropipette aspiration technique. The main works and results in this paper are as follows:
     1. SPEF equipment and experimental parameters
     SPEF equipment was self-assembled by Key Laboratory of High Voltage & Electrical New Technique of Ministry of Education of China, Chongqing University. It consists of circuit of direct current, producing and output of SPEF and collecting and processing system controlled by computer. In our experiments, we fixed voltage(200V), frequency (100Hz), treanment time (10min) and changed the capacitance values (0.01μF and 0.1μF)to investigate the effects of SPEF on biorheological properties.
     2.Effects of SPEF on proliferating dynamics of hepatoma cells
     With MTT assay, the growth and proliferation of hepatoma cells treated by SPEF were evaluted. Results showed that SPEF could inhibit the growth and proliferation of hepatoma cells and high dosage treatment showed a stronger inhibition than that of low dasage treatment. It also showed that G0/G1 phase increase but S phase and G2/M phase decrease after treated by SPEF, which suggested that SPEF could change the distribution of cell cycle and block hepatoma cells entering S phase.
     3. Effects of SPEF on expression of gene involved apoptosis in hepatoma cells
     After exposure to SPEF, Expression of bcl-2 and p53 gene in hepatoma cells was measured by FCM and FITC marked monoclonal antibody quantificationally. It found that SPEF could down-regulate the expression of bcl-2 gene, but expression of p53 gene don’t have any change. It indicated that the apoptosis of hepatoma cells induced by SPEF maybe performed through down-regulate the expression of bcl-2 gene.
     4. Effects of SPEF on viscoelastical properties of hepatoma cells
     Compared with control, both K1 and K2 values of hepatoma cells treated by low dosage SPEF have no change, while K1 of hepatoma cells treated by high dosage SPEF showed an obvious decrease and K2 significantly increase. Viscous coefficientμshowed an increase trend in all treatment groups after exposure to SPEF. As for the eigenvalues of viscoelasticity of hepatoma cells, it showed that the primary deformation have no defference but the maximum deformation of high dasage treatment hepatoma cells increase markedly when compared with control cells. It also showed a smaller rigidity and longer time of creeping deformation than that of control cells.
     5. Effects of SPEF on adhesive force of hepatoma cells to HUVECs
     Adhesive force of low dasage treatment cells to HUVECs present a higher value when compared with control cells. However, adhesive force of high dasage treatment cells to HUVECs reveals no significant difference compared with control cells.
引文
[1] Gao Jin, Young Gang, Xue Kexun, et al. Characteristics of invasiveness of human nasopharyngeal carcinoma cells in organ culture. Path Res Pract, 1982, 174: 325-330.
    [2] 汤钊猷主编. 现代肿瘤学. 上海: 上海医科大学出版社,1993.
    [3] Okino M, Mohri H. Optimal electric condictions in electrical impulse chemotherapy. Japanese Journal of Cancer Research. 1992. 83(10): 1095-1101.
    [4] Hofmann G A, Evans G. Electronic genetic-Physical and biological aspects of cellular electro-manipulation. IEE Eng Med Biol Mag, 1986, 5(4): 6-25.
    [5] Sersa G, Krzic M, Sentjurc M, et al. Reduced blood flow and oxygenation in SA-1 tumours after electrochemotherapy with cisplatin. Br J Cancer. 2002, 87(9):1047-1053.
    [6] Gong H Y, Liu G Z. Effect of electrochemical therapy on immune functions of normal and tumour-bearing mice. Eur J Surg Suppl. 1994;(574): 73-79.
    [7] 陈因良, 陈志宏主编. 细胞培养工程, 第一版, 上海, 华东化工学院出版社, 1992: 57-114.
    [8] Marin V, Kaplanski G, Grès S, Farnarier C, Bongrand P. Endothelial cell culture: protocol to obtain and vultivate human umbilical endothelial cells. Journal of Immunological Methods 2001, 254: 183-190.
    [9] 米 彦,孙才新,姚成果,熊 兰,胡 娅,胡丽娜. 陡脉冲肿瘤治疗仪的研制及应用. 重庆大学学报,2003,26(2):12-14.
    [10] 姚成果,孙才新,米 彦,熊 兰,胡丽娜. 能量可控陡脉冲肿瘤治疗仪的研制. 仪器仪表学报,2003,24(6):636-639.
    [11] 姚成果,孙才新,熊 兰,米 彦,廖瑞金,胡丽娜,胡 娅. 陡脉冲电场对恶性肿瘤细胞杀伤效应的研究. 生物医学工程学杂志,2000,18(4):474-477.
    [12] 司徒镇强 吴军正主编 细胞培养 北京等 世界图书出版公司 1996 :186-187
    [13] 熊 兰,孙才新,米 彦,罗小东,姚成果,王士彬. 陡脉冲诱导在体肿细胞凋亡及分析. 重庆大学学报,2004,27(11):22-25.
    [14] 杨孝军,胡丽娜,李 均,孙才新,熊 兰,姚成果. 低能陡脉冲致人卵巢癌 SKOV23 细胞核 DNA 链断裂损伤的实验研究. 实用妇产科杂志,2004,20(6):343-346.
    [15] Hockenberry DM, Oltvai ZN, Yin XM, Milliman CL, Korsmeyer SJ. Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell 1993; 75: 241-251.
    [16] Hickman ES, Moroni MC, Helin K. The role of p53 and pRB in apoptosis and cancer. Curr Opin Genet Dev 2002; 12: 60-66.
    [17] 阎水忠,赵晓航,吴昊. 细胞凋亡与癌基因. 生物化学与生物物理进展,1994,21(3):222-224.
    [18] Schuler M,Green D R. Mechanisms of p53-dependent apoptosis. Biochem Soc Trans,2001,29(6):684-688.
    [19] Cappello F,Bellafiore M,Palma A,et al. Defective apoptosis and tumorigenesis: role of p53 mutation and Fas/FasL system dysregulation. Eur J Histochem,2002,46:199-208.
    [20] Okuda K. Hepatocellular carcinoma, recent progress. Hepatology, 1992, 15(5): 948-963.
    [21] Evans E, Kukan B. Passive material behavior of granulocytes based on large deformation and recovery after deformation tests. Blood, 1984, 64: 1028-1035.
    [22] Needham D, Hochmuth R M. Rapid flow of passive neutrophils into a 4 micro pipet and measurement of cytoplasmic viscosity. J Biomech Eng, 1990, 112: 269-276.
    [23] Tsai M A, Frank R S, Waugh R E. Passive mechanical behavior of human neutrophils: power-low fluid. Biophys J, 1998, 65: 2078-2088.
    [24] Ben-Ze’ev A. The cytoskeleton in cancer cells. Biochim Biophys Acta, 1985, 780: 197-212.
    [25] Chien S., Sung K.-L. P., Skalak R., et al. Theoretical and experimental studies on viscoelastic properties of erythrocyte membrane. Biophys J, 1978, 24: 463-487.
    [26] Sung K-L P, Schmid-Schonbein G W, Skalak R, et al. Influence of physicochemical factors on rheology of human neutrophils. Biophys J, 1982, 39: 101-106.
    [27] Kawech N , Seif R. Effect of microtubule disorganizing or oversta2 bilizing drugs on the proliferation of rat 3T3 cells and their virally induced transformal derivatives. Cancer Res , 1988 ,48 : 4892).
    [28] 张钢 龙勉 吴泽志, 肝癌细胞粘弹性的实验研究. 解放军医学杂志, 2001 年 3 月第 26 卷第 3 期 P204-206.
    [29] 吴泽志, 张 钢, 龙 勉,等. 秋水仙素和长春花碱对肝癌细胞粘弹性的影响. 生物物理学报, 1998, 14(l): 165-171.
    [30] 吴泽志, 张 钢, 王宪航, 等. 肝细胞粘弹特性及其与细胞骨架结构的相关性研究. 生物医学工程学杂志, 1997, 14(2): 111-114.
    [31] 秦廷武, 杨瑞芳, 蒋稼欢, 蔡绍皙. 大鼠运动力竭后 PMN 在自体血浆及交叉血浆中粘弹性研究. 中国医学物理学杂志, 1998, 15(2): 72-74.
    [32] 宋关斌, 刘保安, 李新平, 等. 金黄色葡萄球菌对中性粒细胞粘弹性的影响. 重庆大学学报(自然科学版), 2002, 25(3): 75-77.
    [33] Sung K-L P, Sung L A, Crimmins M, et al. Dynamic changes in viscoelastic properties in cytotoxic T-lymphocyte- mediated killing. J Cell Sci, 1988, 91: 179-189.
    [34] Chien S, Sung K-L P. Effect of colchicines on viscoelastic properties of neutrophils. Biophys J, 1984, 46: 383-386.
    [35] 吴泽志, 张 钢, 龙 勉,等. 秋水仙素和长春花碱对肝癌细胞粘弹性的影响. 生物物理学报, 1998, 14(l): 165-171.
    [36] 金伯泉主编 . 细胞和分子免疫学 北京等 世界图书出版公司 1998,34-44
    [37] Nocolson G L. Tumor and host molecules important in the organ preference of metastasis. Sem Cancer Biol, 1991, 2: 143-147.
    [38] 高 进. 癌的侵袭与转移——基础研究与临床,第一版, 北京, 北京医科大学中国协和医科大学联合出版社, 1996: 1-2.
    [39] Honn K V, Tang O G. Adhesion molecules and tumor cell interaction with endothelium and subendothelial matrix. Cancer Metastasis Rev, 1990, 11: 353-358.
    [40] Takahashi K. Spontaneous transformation and immortalization of human endothelial cells. Cell Dev Biol, 1990, 25: 265-279.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700