Landberg G, Roos G
Department of Pathology, University of Umeå, Sweden.
Cell Prolif. 1993 Sep;26(5):427-37. doi: 10.1111/j.1365-2184.1993.tb00130.x.
By flow cytometric dual parameter analysis of proliferating cell nuclear antigen (PCNA) and the Ki-67 antigen a detailed cell cycle analysis can be performed. In this study the coordinated expression of these two growth-related antigens was investigated in human haematopoietic cells at entrance into the cell cycle as well as at exit from the cycle. In mitogen-stimulated peripheral blood lymphocytes entering the first cell cycle, the Ki-67 antigen was found to be expressed in S phase cells and not in G1 cells. Thus, the Ki-67 antigen expression in PCNA-positive S phase cells differed between continuously cycling cells and cells entering the cell cycle. Based on this difference, it was possible to visualize and evaluate the recruitment of cells into the first cell cycle from a resting stage. This new cell cycle parameter can give additional information concerning tumour growth. The Ki-67 antigen was also studied during different stages of G1 and was found to be expressed at high levels in early G1 cells compared with other parts of G1.
通过对增殖细胞核抗原(PCNA)和Ki-67抗原进行流式细胞术双参数分析,可以进行详细的细胞周期分析。在本研究中,对这两种与生长相关的抗原在人类造血细胞进入细胞周期以及退出周期时的协同表达进行了研究。在进入第一个细胞周期的有丝分裂原刺激的外周血淋巴细胞中,发现Ki-67抗原在S期细胞中表达,而在G1期细胞中不表达。因此,PCNA阳性S期细胞中Ki-67抗原的表达在持续循环的细胞和进入细胞周期的细胞之间存在差异。基于这种差异,有可能可视化和评估从静止期进入第一个细胞周期的细胞募集情况。这个新的细胞周期参数可以提供有关肿瘤生长的额外信息。还对G1期的不同阶段进行了Ki-67抗原研究,发现与G1期的其他部分相比,Ki-67抗原在早期G1期细胞中高表达。