摘要
培养B958细胞,分离EB病毒,转染外周血和扁桃体淋巴细胞,建立永生化的LCLs和TLCL细胞株;带有wtP53基因的LCLs在DNA损伤剂———顺铂处理前未检出p53蛋白,经顺铂处理后,LCLs随作用时间延长细胞存活率明显下降、p53蛋白水平升高、DNA电泳显出梯状带;含mtP53基因的淋巴瘤细胞在顺铂处理前可检出高浓度的p53蛋白,经顺铂处理后,细胞存活率与p53蛋白并无明显改变.这些结果表明:顺铂引起细胞DNA损伤、激活wtp53蛋白的表达。
Epatein Barr Virus(EBV) is isolated from B95 8 cell line, the primary B lymphocytes from human blood and tonsil tissue are transfected with EBV in order to gain immortalized lymphoblastoid cell lines(LCLs) and tonsil lymphoblastoid cell lines(TLCL). The LCLs and TLCL contain wt p53 gene, and do not express p53 proteins before treatment with cisplatin. Cell viability are decreased, p53 proteins are accumulated,and DNA ladders appear in LCLs and TLCL with time extension after treating with 10 mg/L. Lymphoma cell lines(BJAB, Raji, Ramos, Molt4) carring mutant p53 gene show accumulation of p53 protein before treatment with cisplatin. In paralleled experiment, the lymphoma cell lines appear relatively resistant to the doses of cisplatin. The results suggest that cisplatin cause DNA damage of LCLs and TLCL, activate wt p53 expression, and cells with DNA damage enter the pathway of apoptosis induced by wt p53.
出处
《生物化学与生物物理进展》
SCIE
CAS
CSCD
北大核心
1999年第2期150-153,共4页
Progress In Biochemistry and Biophysics
基金
广东省高教厅自然科学重点资助项目
李嘉诚科研基金