Barfod I H, Barfod N M
Cell Tissue Kinet. 1980 Jan;13(1):1-8. doi: 10.1111/j.1365-2184.1980.tb00444.x.
A method for the evaluation of cell-production rates is described which combines flow cytometry (FCM) and the stathmokinetic method. By means of FCM it is possible to estimate the distribution of cells with G1, S and (G2 + M) DNA content in a population. As this method gives the relative (G2 + M) DNA content of cells within the cell cycle, it may be possible to evaluate cell-production rates by this technique. In the present study it was found that administration of a metaphase-arresting (stathmokinetic) agent, vincristine sulphate (VS), to asynchronous cell populations of three different murine tumour cell lines in vitro increased the peak representing cells with (G2 + M) DNA content as the number of mitotic (M) cells increased during the period of treatment. The accumulation of mitotic cells was determined by cell counts on smears under the microscope and compared with increase in the (G2 + M) DNA peak measured by FCM as a function of time after the administration of VS. Good agreement was obtained between the cell-production rates as estimated by FCM and by mitotic counts in all three cell lines investigated.
描述了一种评估细胞生成率的方法,该方法结合了流式细胞术(FCM)和静止期动力学方法。通过FCM可以估计群体中具有G1、S和(G2+M)DNA含量的细胞分布。由于该方法给出了细胞周期内细胞的相对(G2+M)DNA含量,因此有可能通过该技术评估细胞生成率。在本研究中发现,向三种不同小鼠肿瘤细胞系的异步细胞群体体外施用中期阻滞(静止期动力学)剂硫酸长春新碱(VS),随着处理期间有丝分裂(M)细胞数量的增加,代表具有(G2+M)DNA含量的细胞的峰值增加。通过显微镜下涂片的细胞计数确定有丝分裂细胞的积累,并与施用VS后作为时间函数通过FCM测量的(G2+M)DNA峰值的增加进行比较。在所研究的所有三种细胞系中,通过FCM估计的细胞生成率与有丝分裂计数之间获得了良好的一致性。