Luk C K, Keng P C, Sutherland R M
Cancer Res. 1985 Mar;45(3):1020-5.
A quiescent [denoted as Q(G0/G1)] subpopulation was isolated from EMT6/Ro-fed plateau monolayers by centrifugal elutriation. The median Coulter volume of these cells was significantly smaller than that of the original population from which they were elutriated. Using two-step acridine orange staining and dual parameter flow cytometric analysis, over 95% of quiescent cells were found to have G1 DNA content, and 80% of the cells had a decreased RNA content as compared to rapidly proliferating exponential G1 cells. After labeling for 24 hr (two doubling times) with [3H]thymidine, less than 2% of the quiescent cells incorporated [3H]thymidine as measured by autoradiography. The colony-forming efficiency of these cells was not significantly different from that of exponential cells. When such Q(G0/G1) cells were replated in fresh medium at a lower density, there was a lag time of 30 hr before any increase in cell number was detected, after which the cell-doubling rate matched that of exponential culture. Results obtained from the radiation dose-response curves showed that quiescent (G0/G1) cells were more radiosensitive than exponential G1 or unseparated fed plateau cells.
通过离心淘析从用EMT6/Ro饲养的平台期单层细胞中分离出一个静止的[记为Q(G0/G1)]亚群。这些细胞的平均库尔特体积明显小于淘析它们的原始群体。使用两步吖啶橙染色和双参数流式细胞术分析,发现超过95%的静止细胞具有G1期DNA含量,并且与快速增殖的指数期G1细胞相比,80%的细胞RNA含量降低。用[3H]胸苷标记24小时(两个倍增时间)后,通过放射自显影测量,不到2%的静止细胞掺入了[3H]胸苷。这些细胞的集落形成效率与指数期细胞没有显著差异。当将此类Q(G0/G1)细胞以较低密度重新接种到新鲜培养基中时,在检测到细胞数量增加之前有30小时的延迟期,之后细胞倍增率与指数培养物的倍增率相匹配。从辐射剂量反应曲线获得的结果表明,静止的(G0/G1)细胞比指数期G1细胞或未分离的用EMT6/Ro饲养的平台期细胞对辐射更敏感。