Tinnemans M M, Lenders M H, ten Velde G P, Blijham G H, Ramaekers F C, Schutte B
Department of Molecular Cell Biology and Genetics, University of Limburg, Maastricht, The Netherlands.
Cytometry. 1995 Apr 1;19(4):326-33. doi: 10.1002/cyto.990190407.
The human small cell lung cancer cell line NCI-H82 was used to study the effect of nutritional status on cell proliferative parameters. Incorporation of bromodeoxyuridine (BrdUrd) was used to characterize actively proliferating cells and to obtain information on cell cycle dynamics. During several days, in which the culture medium was not changed, a gradual decrease in overall cell growth, labeling index, and vitality was observed. Simultaneously, an increase in the number of S-phase cells that did not incorporate BrdUrd was noticed. From a more detailed kinetic study on d 6 of nutrient depletion, it appeared that, although the cells incorporated BrdUrd, they stopped cycling. When the same cells were regrown in fresh culture medium, a delay of 10 h in G1-phase entry and exit was measured. After this delay the cells resumed the cell cycle at normal phase transit rates. In addition, BrdUrd unlabeled S-phase cells were gradually lost from the culture. Bivariate flow cytometric DNA/proliferating cell nuclear antigen (PCNA) and DNA/Ki67-antigen analyses confirmed a delay in G1 phase entry and exit. In this paper we show that nutrient depletion can cause cell cycle arrest as indicated by the occurrence of BrdUrd unlabeled S-phase cells. This arrest could lead to overestimation of kinetic parameters such as S-phase transit time (Ts) and potential time (Tpot) as determined after in vivo labeling of tumors.
人类小细胞肺癌细胞系NCI-H82用于研究营养状况对细胞增殖参数的影响。采用溴脱氧尿苷(BrdUrd)掺入法来表征活跃增殖细胞并获取细胞周期动力学信息。在数天内,培养基未更换,观察到总体细胞生长、标记指数和活力逐渐下降。同时,未掺入BrdUrd的S期细胞数量增加。从营养耗竭第6天的更详细动力学研究来看,虽然细胞掺入了BrdUrd,但它们停止了循环。当相同细胞在新鲜培养基中重新生长时,测量到G1期进入和退出延迟了10小时。在此延迟之后,细胞以正常的时相转换速率恢复细胞周期。此外,未标记BrdUrd的S期细胞逐渐从培养物中丢失。双变量流式细胞术DNA/增殖细胞核抗原(PCNA)和DNA/Ki67抗原分析证实了G1期进入和退出的延迟。在本文中,我们表明营养耗竭可导致细胞周期停滞,这由未标记BrdUrd的S期细胞的出现所表明。这种停滞可能导致对动力学参数的高估,如在肿瘤体内标记后确定的S期转换时间(Ts)和潜在时间(Tpot)。