Wiezsaecker M, Hoshino T, Kobayashi S
Cell Tissue Kinet. 1981 Sep;14(5):575-80. doi: 10.1111/j.1365-2184.1981.tb00562.x.
The colony-forming efficiency of 9L rat gliosarcoma cells was unaffected by treatment with 0.1 muCi/ml of [3H]TdR. However, when cells were treated with 1 or 10 muCi/ml of [3H]Tdr, cell growth was reduced and cell survival decreased. When monolayer 9L cells were treated with 1 muCi/ml of [3H]TdR for up to 72 hr, approximately 5% survived, which is closely related to the percentage of non-cycling cells in this system. When cells were treated with 10 muCi/ml of [3H]TdR for 72 hr, less survival was observed. The additional cell kill observed may be induced by [3H]TdR released from doomed cells into petri dishes during the incubation period of the colony-formation assay.
9L大鼠胶质肉瘤细胞的集落形成效率不受0.1微居里/毫升[3H]胸腺嘧啶核苷([3H]TdR)处理的影响。然而,当细胞用1或10微居里/毫升的[3H]TdR处理时,细胞生长受到抑制且细胞存活率下降。当单层9L细胞用1微居里/毫升的[3H]TdR处理长达72小时时,约5%的细胞存活,这与该系统中处于非增殖周期细胞的比例密切相关。当细胞用10微居里/毫升的[3H]TdR处理72小时时,观察到的存活率更低。在集落形成试验的孵育期内,从死亡细胞释放到培养皿中的[3H]TdR可能诱导了额外的细胞杀伤。