Takita Morihito, Furuya Tomoko, Sugita Tomoya, Kawauchi Shigeto, Oga Atsunori, Hirano Takashi, Tsunoda Shinichi, Sasaki Kohsuke
Department of Pathology, Yamaguchi University School of Medicine, Ube, Japan.
Cytometry A. 2003 Sep;55(1):24-9. doi: 10.1002/cyto.a.10066.
A novel high-throughput analysis, cell array system, was developed for an extensive study of the expression of genes and/or the degradation of gene products at the cellular level. To exemplify the usefulness of this system, we showed the changes in the expression level of cyclin A and B1 during the cell cycle in a single experiment.
We used the cell array system to chase the changes in cyclin A and B1 expression during the cell cycle in HeLa cells. Cells were synchronized by mitotic selection and thymidine-hydroxyurea methods. Cells were harvested at intervals of 1 h from 0 through 23 h. These 48 cell samples were spotted on a circle of the cell array glass slide. Cyclin A and B1 were immunologically stained with Alexa Fluor 488, and nuclear DNA was stained with propidium iodide. The amount of cyclins and nuclear DNA were simultaneously measured by a laser scanning cytometer.
Both cyclins were expressed in a cell cycle-dependent manner as previously reported. The precise time-course of the expression level of cyclins were obtained at a single experiment with this cell array system.
This study indicates that the cell array system is valuable to analyze temporal course of protein expression in relation to the cell cycle position and, that it facilitates antigen expression studies at the cellular level in multiple samples.
开发了一种新型高通量分析细胞阵列系统,用于在细胞水平上广泛研究基因表达和/或基因产物的降解。为了证明该系统的实用性,我们在一次实验中展示了细胞周期中细胞周期蛋白A和B1表达水平的变化。
我们使用细胞阵列系统追踪HeLa细胞在细胞周期中细胞周期蛋白A和B1表达的变化。通过有丝分裂选择和胸腺嘧啶-羟基脲方法使细胞同步化。从0至23小时每隔1小时收获细胞。将这48个细胞样本点样在细胞阵列载玻片的一个圆圈上。用Alexa Fluor 488对细胞周期蛋白A和B1进行免疫染色,并用碘化丙啶对核DNA进行染色。通过激光扫描细胞仪同时测量细胞周期蛋白和核DNA的量。
如先前报道,两种细胞周期蛋白均以细胞周期依赖性方式表达。使用该细胞阵列系统在一次实验中获得了细胞周期蛋白表达水平的精确时间进程。
本研究表明,细胞阵列系统对于分析与细胞周期位置相关的蛋白质表达的时间进程很有价值,并且它有助于在多个样本的细胞水平上进行抗原表达研究。