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1. 苏州大学附属第一医院核医学科
2. 苏州大学放射医学与公共卫生学院,苏州,215006
3. ,苏州,215007
纸质出版日期:2006-05-01
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[1]苏成海,法逸华,许玉杰,范我.低剂量率γ射线杀伤肿瘤细胞机制的实验研究[J].核技术,2006(05):362-367.
SU Chenghai1 FA Yihua1 XU Yujie2 FAN Wo2 1. Study on the anti-cancer mechanisms of low dose-rate γ irradiation[J]. Nuclear techniques, 2006, (5): 362-367.
用60Co源以1Gy/min剂量率照射Hela细胞
剂量分别为1、2、5、10、15Gy。用AnnexinV和PI双染法观察凋亡细胞形态;DNA梯形条带证实凋亡存在;克隆形成分析细胞增殖能力。结果显示:(1)Hela细胞凋亡率随照射剂量和时间的增加呈上升趋势
照射后168h组各剂量点凋亡率高于其他各时间组。2Gy以下时凋亡率改变不大
达5Gy时凋亡率显著增加
且达峰值(72.57±2.04)%(P<0.001)。(2)早期凋亡细胞
PS外翻
胞膜呈绿色荧光圈。凋亡晚期出现AnnexinV-FITC及PI染色均阳性的外绿内红的细胞图像。坏死细胞则为红色。(3)凋亡细胞碎片呈“梯状”条带。(4)1Gy/min的剂量率照射
剂量为2—15Gy
克隆形成率由(58.95±0.36)%降至(1.67±0.35)%(P<0.001)。表明低剂量率γ射线照射可诱导Hela细胞凋亡
其凋亡率与照射剂量相关
在5Gy时凋亡率最高。
To investigate appropriate dose range in low-dose-rate γ irradiation and to establish a useful method for the research of radioactive biological effect produced by low does-rate γ irradiation
we have studied apoptosis of Hela carcinoma cells induced by different low dose rates of γ irradiation in vitro. The cultured cells were exposed to defined radiation doses from a 60Co therapy source. The radiation source delivered a dose rate of 1Gy/min and gave total dose of 1
2
5
10 and 15 Gy respectively. Using Annexin V labeled by fluorescein and PI
followed by flow cytometry and DNA ladder analysis and confocal microscope
apoptotic cells were detected and quantified. The re- sults are as follows: (1) Determination of apoptosis by flow cytometry indicated that percentage of apoptotic cells was increasing with dose and time. When cells were cultured for 168 h after irradiation
the highest percentage of apop- tosis was yielded in all groups. When the cells were irradiated with 1—2 Gy
no significant increase in the number of apoptotic cells could be seen. After a total dose of 5 Gy
however
a significant increase in the ratio of apop- totic/nonapoptotic cells was observed
and apoptosis reached a peak level of (72.57±2.04)% (P <0.001). (2) The typi- cal appearance of Hela cells stained by annexin V-Fluos for detection of apoptosis exhibited a plasma mem-brane-localized fluorescence that is an early sign of apoptosis under laser confocal microscope. PI entered into the cells slowly while in later apoptosis
with special laser which were red in center and green around
however
necrotic cell only emitted red laser. (3)The presence of apoptotic cells were confirmed by the DNA ladder formation assay
with typical formation of apoptotic fragments. DNA laddering reached the greatest after a single radiation dose of 5 Gy. (4) Over the dose interval from 2 to 15 Gy with a dose rate of 1 Gy/min
the survival of the cells decreased from (58.95±0.36)% to (1.67±0.35)% (P <0.001) by clonogenic assay. It was concluded that the low-dose
low-dose-rate γ irradiation delivered by 60Co sources to Hela cells can induce a significant apoptosis rate
and a maximum level of apoptosis as high as (72.57±2.04)% for an irradiation dose of 5Gy can be reached .
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