Landberg G, Roos G
Department of Pathology, University of Umeå, Sweden.
Acta Oncol. 1991;30(8):917-21. doi: 10.3109/02841869109088244.
Human hematopoietic cell lines and fresh lymphoma cells were investigated for their expression of proliferating cell nuclear antigen (PCNA) and Ki-67 antigen using flow cytometry. Ki-67 was detected with a monoclonal antibody and the PCNA content was determined using a human auto-antiserum and in some cases a monoclonal antibody (PC10). The autoantibody to PCNA was found to recognize S-phase cells and the number of positively stained cells was significantly correlated with the S-phase fraction determined from DNA-histograms. There was also a strong association between Ki-67 positivity and the fraction of S-phase cells. By dual parameter analysis of Ki-67 and PCNA detected by the autoantibody a detailed cell cycle analysis could be performed of the lymphoma samples. The recently described PC10 monoclonal antibody was found by FCM to be a good proliferation marker recognizing cycling cells after methanol and detergent treatment, however without any specific cell cycle phase preference.
利用流式细胞术研究了人造血细胞系和新鲜淋巴瘤细胞中增殖细胞核抗原(PCNA)和Ki-67抗原的表达情况。用单克隆抗体检测Ki-67,使用人自身抗血清并在某些情况下使用单克隆抗体(PC10)测定PCNA含量。发现针对PCNA的自身抗体可识别S期细胞,且阳性染色细胞的数量与从DNA直方图确定的S期分数显著相关。Ki-67阳性与S期细胞分数之间也存在很强的关联。通过对自身抗体检测到的Ki-67和PCNA进行双参数分析,可以对淋巴瘤样本进行详细的细胞周期分析。通过流式细胞术发现,最近描述的PC10单克隆抗体是一种良好的增殖标志物,在甲醇和去污剂处理后可识别循环细胞,但没有任何特定的细胞周期阶段偏好。