检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王毅[1] 舒逸[1] 苑俊涛 陈卉[1] 邹琳[1]
机构地区:[1]重庆医科大学附属儿童医院临床分子医学中心//儿童发育疾病研究教育部重点实验室//儿科学重庆市重点实验室//重庆市儿童发育重大疾病诊治与预防国际科技合作基地,重庆400014
出 处:《南方医科大学学报》2016年第1期78-82,共5页Journal of Southern Medical University
基 金:国家自然科学基金(81373444,81570142)
摘 要:目的探讨Tal1对T-ALL细胞增殖及其机制的影响。方法用Tal1慢病毒感染T-ALL细胞株Jurkat,建立稳定的Tal1敲降细胞株(Jurkat-si Tal1)和Tal1过表达细胞株(Jurkat-T1),及si RNA阴性对照细胞(Jurkat-mock1)和过表达阴性对照细胞(Jurkatmock2)。CCK-8检测细胞生长能力;流式细胞术检测细胞周期;Real-time RT-PCR和Western blot检测周期蛋白依赖性激酶抑制因子2(CDKN2A)、周期蛋白依赖性激酶抑制因子1(CDKN2B)m RNA和蛋白表达。结果成功建立Jurkat稳定转染细胞株。CCK8结果表明细胞Jurkat-T1与Jurkat-mock2相比,细胞生长更快,而Jurkat-si Tal1与Jurkat-mock1相比,细胞生长明显减缓。流式细胞术检测细胞周期发现,Jurkat-si Tal1与Jurkat-mock1相比G0/G1期增加,S期减少;而Jurkat-T1与Jurkat-mock2相比,G0/G1期减少,S期增加。Real-time RT-PCR和Western blot结果显示Tal1抑制Jurkat细胞内CDKN2A、CDKN2B的m RNA和蛋白表达。结论 Tal1可以促进T淋巴白血病细胞Jurkat增殖;促进Jurkat细胞由G0/G1期向S期转换,其可能通过Tal1抑制G0/G1和S期负调控蛋白CDKN2A、CDKN2B的表达。Objective To investigate the role of Tal1 gene, which is aberrantly expressed in 40%- 60% of patients with T lymphocytic leukemia(T-ALL), in the proliferation of T-ALL cells. Methods We established stable Jurkat-si Tal1 and Jurkat-T1 cell lines by trasnfecting T-ALL Jurkat cells with lentiviral vectors to knock-down or overexpress Tal1. Jurkat cells transfected with negative control si RNAs for Tal1 knock- down(Jurkat- mock1) and over- expression(Jurkat- mock2) served as the control cells. The proliferation of the cells lines was assessed using CCK- 8 assay, and the cell cycle distribution was determined by flow cytometry. The m RNA and protein expressions of cyclin-dependent kinase inhibitor 2(CDKN2A) and cyclin-dependent kinase inhibitor 1(CDKN2B) were measured by real- time RT- PCR and Western blotting, respectively. Results Jurkat- T1 cells showed more active proliferation in vitro than Jurkat-mock2 cells, while Jurkat-si Tal1 cells showed slower growth than Jurkatmock1 cells. In Jurkat-T1 cells, G0/G1 phase cells were decreased and S phase cells increased compared with Jurkat-mock2 cells,and Jurkat-si Tal1 cells showed increased G0/G1 phase cells and decreased S phase cells compared with Jurkat-mock1 cells. Realtime RT- PCR and Western blotting showed that Tal1 inhibited the cellular expression of CDKN2 A and CDKN2 B at both m RNA and protein levels. Conclusion Tal1 promotes the growth and the transition from G0/G1 phase to S phase in T-ALL cells Jurkat by inhibiting the expressions of G0/G1 and S phase negative regulatory proteins CDKN2 A and CDKN2 B.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.169