Mares V, Giordano P A, Mazzini G, Lisá V, Pellicciari C, Scherini E, Bottiroli G, Drobnik J
Histochem J. 1987 Apr;19(4):187-94. doi: 10.1007/BF01680628.
C6 glioma cells (CCL 107) were cultured for three days and then treated with cis-dichlorodiamineplatinum (cis-DDP) at doses of 0.2-10 micrograms/ml medium. Changes in DNA synthesis and DNA content, as well as morphology of cells and chromatin distribution, were examined from the first post-treatment day onwards. The number of cells labelled with [3H]thymidine, detected autoradiographically, decreased after treatment with 0.2-10 micrograms/ml by approximately one half on post-treatment day 1 and diminished further by the third day after treatment. The labelled cells were entirely absent only after treatment with 10 micrograms/ml, 7 days post-treatment. Mitoses decreased from 1.4-0.6% by post-treatment day 1 and completely disappeared by day 3 (1 microgram/ml). Feulgen cytophotometry and propidium iodide cytofluorimetry revealed accumulation of cells in the S-phase, especially the latter part (0.5 and 1.0 micrograms/ml, post-treatment day 1) and subsequently also in G2 phase (post-treatment day 3). Incomplete cyto- and karyokinesis in some cycling cells was indicated by an increased number of binucleate cells and nuclei of higher ploidy classes. Labelled cells with intermediate DNA values were, on average, labelled less intensively, as was revealed by simultaneous measurements of DNA content and [3H]thymidine incorporation. Some cells displayed reduction in grain density over heterochromatin clumps. This would be in agreement with the late S-phase block of DNA replication. After post-treatment day 3 the density of cells in cultures was substantially lower.(ABSTRACT TRUNCATED AT 250 WORDS)
C6胶质瘤细胞(CCL 107)培养三天,然后用浓度为0.2 - 10微克/毫升培养基的顺式二氯二氨铂(顺铂)处理。从处理后的第一天起,检测DNA合成、DNA含量的变化以及细胞形态和染色质分布。经放射自显影检测,用0.2 - 10微克/毫升处理后,[3H]胸腺嘧啶核苷标记的细胞数量在处理后第1天减少约一半,处理后第3天进一步减少。仅在10微克/毫升处理后,处理后7天标记细胞完全消失。有丝分裂从处理后第1天的1.4 - 0.6%下降,到第3天(1微克/毫升)完全消失。福尔根细胞光度法和碘化丙啶细胞荧光测定法显示细胞在S期积累,特别是后期(处理后第1天,0.5和1.0微克/毫升),随后在G2期也有积累(处理后第3天)。双核细胞数量增加和更高倍体类别的细胞核表明一些循环细胞中存在不完全的胞质分裂和核分裂。通过同时测量DNA含量和[3H]胸腺嘧啶核苷掺入量发现,具有中等DNA值的标记细胞平均标记强度较低。一些细胞在异染色质团块上的颗粒密度降低。这与DNA复制的S期晚期阻滞一致。处理后第3天,培养物中的细胞密度显著降低。(摘要截断于250字)