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Caspase-3对5-ALA诱导鳞状细胞癌Colo-16细胞凋亡效应的影响
引用本文:徐劲,乔丽,杨志勇,刘玮. Caspase-3对5-ALA诱导鳞状细胞癌Colo-16细胞凋亡效应的影响[J]. 武警医学, 2017, 28(3): 232-234. DOI: 10.3969/j.issn.1004-3594.2017.03.004
作者姓名:徐劲  乔丽  杨志勇  刘玮
作者单位:100142 北京,空军总医院皮肤科
摘    要: 目的 探讨半胱氨酸天冬氨酸蛋白酶3(Caspase-3)对光敏剂5-氨基酮戊酸(5-ALA)诱导鳞状细胞癌Colo-16细胞凋亡效应的影响。方法 取对数生长期的Colo-16细胞用于实验,将细胞分为对照组、5-ALA-光动力疗法(photodynamic therapy,PDT)组和Caspase-3抑制剂组(Z-DEVD-FMK),对照组不给予光敏剂和照光处理,5-ALA-PDT组给予0.4 mg/ml的5-ALA避光孵育4 h后,采用(功率密度10 mW/cm2,能量密度2.5 J/cm2)激光照射3 min,之后继续培养12 h。Caspase-3抑制剂组除孵育时同时加入Z-DEVD-FMK(终浓度40 μmol),其余处理与5-ALA-PDT组相同。实验后收集各组细胞,通过免疫荧光观察各组细胞胞内Caspase-3荧光强度的变化,通过流式细胞术检测活性Caspase-3阳性细胞百分率和细胞凋亡率。结果 免疫荧光结果发现对照组和Caspase-3抑制剂组Colo-16细胞胞浆中有微弱绿色荧光,表明Caspase-3表达量低,而5-ALA-PDT组中绿色荧光显著增强,表明其胞浆内Caspase-3含量显著增高。流式细胞仪的检测结果显示,对照组、5-ALA-PDT组和Caspase-3抑制剂组active-Caspase-3阳性细胞百分率分别为(2.26±0.16)%、(32.16±1.31)%和(3.36±0.31)%,5-ALA-PDT组高于对照组和Caspase-3抑制剂组,差异有统计学差异(P<0.05)。对照组、5-ALA-PDT组和Caspase-3抑制剂组的凋亡率分别为(2.35±0.22)%、(31.55±3.68)%和(11.46±2.25)%,三组之间两两比较,差异都有统计学意义(P<0.01)。结论 5-ALA-PDT可以诱导Colo-16细胞发生凋亡,且这种效应与caspase-3的激活密切相关。

关 键 词:半胱氨酸天冬氨酸蛋白酶3   鳞状细胞癌   Colo-16细胞   5-氨基酮戊酸   细胞凋亡  
收稿时间:2016-10-20

Effects of caspase 3 on apoptosis of squamous-cell carcinoma Colo-16 cells induced by 5-ALA-PDT
XU Jin,QIAO Li,YANG Zhiyong,LIU Wei. Effects of caspase 3 on apoptosis of squamous-cell carcinoma Colo-16 cells induced by 5-ALA-PDT[J]. Medical Journal of the Chinese People's Armed Police Forces, 2017, 28(3): 232-234. DOI: 10.3969/j.issn.1004-3594.2017.03.004
Authors:XU Jin  QIAO Li  YANG Zhiyong  LIU Wei
Affiliation:Department of Dermatology, General Hospital of Air Force, Beijing 100142, China
Abstract:Objective To investigate the role of caspase-3 in the apoptosis of squamous-cell carcinoma Colo-16 cells induced by 5-ALA-PDT.Methods Colo-16 cells in the logarithmic growth phase were divided into three groups:control group,5-ALA photodynamic therapy (PDT) group,and caspase-3 inhibitor group (Z-DEVD-FMK).Control group was not given photosensitizer or light treatment.5-ALA PDT group was exposed to 3-minute laser irradiation at a power density of 10 mW/cm2 and energy density of 2.5 J/ cm2 after 4 hours of dark incubation with 0.4 mg/ml 5-ALA before being cultured for 12 hours.Caspase3 inhibitor group was treated in the same way as 5-ALA PDT group except that Z-DEVD-FMK at a final concentration of 40 μmol was added during incubation.Cells in each group were collected after experiment,the changes of intracellular caspase-3 fluorescence intensity were observed by immunofluorescence,and the percentage of positive cells and apoptosis rate of active caspase-3 were detected by flow cytometry.Results Immunofluorescence results showed that there was weak green fluorescence in the cytoplasm of Colo-16 cells in control group and Caspase-3 inhibitor group,indicating a low expression of caspase-3,while green fluorescence was significantly enhanced in 5-ALA-PDT group,showing a significant increase of caspase-3 content in cytoplasm of Colo-16 cells.Flow cytometry results showed that the respective percentage of active caspase-3 positive cells was (2.26 ± 0.16) %,(32.16 ± 1.31) % and (3.36 ± 0.31) % in control group,5-ALA PDT group and caspase-3 inhibitor group respectively.The difference was statistically significant (P < 0.05).The apoptosis rate of control group,5-ALA PDT group and caspase-3 inhibitor group was (2.35 ± 0.22) %,(31.55 ± 3.68) % and (11.46 ± 2.25) %,respectively.Paired comparison was made between the three groups,and the differences were statistically significant (P < 0.01).Conclusions The apoptosis of Colo-16 cells induced by 5-ALA-PDT is closely related to the activation of caspase-3.
Keywords:caspase-3  human cutaneous carcinoma cell line  Colo-16  5-ALA-PDT  apoptosis
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