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。
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.
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
Key words
caspase-3 /
human cutaneous carcinoma cell line /
Colo-16 /
5-ALA-PDT /
apoptosis
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] 刘慧龙,刘端祺,介雅慧,等. 激光光动力疗法治疗皮肤恶性肿瘤的临床研究[J]. 解放军医学杂志,2007,32(4): 396-397.
[2] Dolmans D E,Fukumura D,Jain R K. Photodynamic therapy for cancer[J]. Nat Rev Cancer,2003,3(5):380-387.
[3] Buytaert E,Dewaele M,Agostinis P. Molecular effectors of multiple cell death pathways initiated by photodynamic therapy [J]. Biochim Biophys Acta, 2007, 1776(1): 86-107.
[4] Garg A D,Nowis D,Golab J,et al. Photodynamic therapy: illuminating the road from cell death towards anti-tumour immunity [J]. Apoptosis, 2010, 15(9): 1050-1071.
[5] Kim K H, Park J J. The effects of photodynamic therapy in upper-gastrointestinal malignant diseases [J]. Gut Liver, 2010, 4(Suppl1): S39-S43.
[6] Tirapelli L F, Morgueti M, Cunha Tirapelli D P, et al. Apoptosis in glioma cells treated with PDT [J]. Photomed Laser Surg, 2011, 29(5): 305-309.
[7] Castano A P, Demidova T N, Hamblin M R. Mechanisms in photodynamic therapy: part one-photo sensitizers, photochemistry and cellular localization [J]. Photodiagn Photodyn, 2004, 1(4): 279-293.
[8] Yang L, Wei Y, Xing D, et al. Increasing the efficiency of photodynamic therapy by improved light delivery and oxygen supply using an anticoagulant in a solid tumor model [J]. Lasers Surg Med,2010,42(7):671-679.
[9] Weiss A, den Bergh H V, Griffioen A W, et al. Angiogenesis inhibition for the improvement of photodynamic therapy: The revival of a promising idea [J]. Biochim Biophys Acta, 2012, 1826(1): 53-70.
[10] Kessel D, Oleinick N L. Initiation of autophagy by photodynamic therapy [J]. Methods Enzymol, 2009, 453: 1-16.
[11] Ji H T, Chien L T, Lin Y H, et al. 5-ALA mediated photodynamic therapy induces autophagic cell death via AMP-activated protein kinase [J]. Mol Cancer, 2010, 9(4): 91-101.