Masunaga S, Ono K, Mitsumori M, Abe M
Radiation Oncology Research Laboratory, Kyoto University, Osaka.
Jpn J Cancer Res. 1993 Nov;84(11):1130-5. doi: 10.1111/j.1349-7006.1993.tb02812.x.
5-Bromo-2'-deoxyuridine (BUdR) was injected into SCC VII or EMT6/KU tumor-bearing mice intraperitoneally to label all the proliferating tumor cells. First, the mice were irradiated with X-rays at a dose of 10 Gy, followed by a dose of 0-20 Gy at 0, 12, 24 or 48 h later. During the interval, no BUdR was injected. Immediately after the second irradiation, the tumors were excised and trypsinized. The micronucleus (MN) frequency in cells without BUdR labeling was determined by means of incubation with cytochalasin-B (a cytokinesis-blocker) and immunofluorescence staining for BUdR. When the tumors were not pretreated with BUdR before the first irradiation, the MN frequency in all tumor cells was determined. To determine the labeling indices of SCC VII and EMT6/KU tumors at the time of the second irradiation, each group also included mice that were continuously administered BUdR until just before the second irradiation using mini-osmotic pumps which had been implanted subcutaneously 5 days before the first irradiation. The MN frequency of all tumor cell populations obtained immediately after the second irradiation decreased in proportion to the increase in interval time. However, in both tumor systems, the MN frequency of unlabeled cell populations, which could be regarded as quiescent cells in the tumors at the time of the first irradiation, was raised with increase in the interval time. In addition, the labeling index at the second irradiation was higher than that at the first irradiation. These findings support the occurrence of recruitment from quiescent to proliferating state during fractionated irradiation.
将5-溴-2'-脱氧尿苷(BUdR)腹腔注射到荷SCC VII或EMT6/KU肿瘤的小鼠体内,以标记所有增殖的肿瘤细胞。首先,小鼠接受10 Gy的X射线照射,然后在0、12、24或48小时后再接受0 - 20 Gy的照射。在此间隔期间,不注射BUdR。第二次照射后立即切除肿瘤并进行胰蛋白酶处理。通过与细胞松弛素B(一种胞质分裂阻断剂)孵育并对BUdR进行免疫荧光染色,测定未用BUdR标记的细胞中的微核(MN)频率。当肿瘤在第一次照射前未用BUdR预处理时,测定所有肿瘤细胞中的MN频率。为了确定第二次照射时SCC VII和EMT6/KU肿瘤的标记指数,每组还包括使用在第一次照射前5天皮下植入的微型渗透泵持续给予BUdR直至第二次照射前的小鼠。第二次照射后立即获得的所有肿瘤细胞群体的MN频率随间隔时间的增加而呈比例下降。然而,在这两种肿瘤系统中,未标记细胞群体(可被视为第一次照射时肿瘤中的静止细胞)的MN频率随间隔时间的增加而升高。此外,第二次照射时的标记指数高于第一次照射时的标记指数。这些发现支持了在分次照射过程中存在从静止状态向增殖状态的细胞募集现象。