摘要
目的观察EBV┐BHRF1基因阳性(SUNE┐1、Raji和B95┐8)与阴性(K562、YAC)细胞株对3种诱导细胞凋亡(apop┐tosis)因素(无血清培养48小时,43℃作用10分钟或2×10-6mol/L地塞米松作用24小时)的抵抗力差异。方法PCR扩增EBV┐BHRF1基因片段诱导后经电镜及电泳DNA检测细胞凋亡。结果分别从B95┐8、Raji及人低分化鼻咽癌细胞株(SUNE┐1)DNA中扩增出EB病毒的BHRF1全基因片段,而K562、YAC细胞株则不含该基因片段。分别经上述3种方法处理后,前3种细胞株的形态及DNA电泳行为未发生明显改变,而后2种细胞株则出现典型的细胞凋亡特征,即细胞核凝缩,细胞膜及细胞器基本保持完整;DNA电泳出现梯形(Ladder)条带。
bjective To observe the difference between EBVBHRF1 gene positive and negative cell lines against 3 kinds of apoptosis inducing factors. Methods These cell lines were cultured in ①the absence of fetal calf serum for 48 h ②43℃ for 10 min,and ③2×10-6 mol/L dexamethasone for 24 h.Polymerase chain reaction (PCR) and apoptosis inducing and detecting methods were used. Results EBVBHRF1 gene fragment was amplified from B958、Raji and SUNE1 cell lines with PCR technique,while K562 and YAC cell lines were negative.The results against 3 kinds of apoptosis inducing factors from electron microscopy and agarose gel electrophoresis indicated that apoptosis appeared in BHRF1 genenegative cell lines,while BHRF1 genepositive cell lines were normal. Conclusion EBVBHRF1 gene is one of the important factors in suppressing its host cell's apoptosis。
出处
《肿瘤》
CAS
CSCD
北大核心
1998年第3期129-130,共2页
Tumor
基金
广东省科委青年基金
华南生物中心基金