Sonodynamic therapy induces apoptosis of human leukemia HL-60 cells in the presence of protoporphyrin IX

被引:14
作者
Su, Xiaomin [1 ,3 ]
Wang, Xiaobing [1 ]
Zhang, Kun [1 ]
Yang, Shuang [1 ]
Liu, Quanhong [1 ]
Leung, Albert W. [2 ]
Xu, Chuanshan [2 ]
Wang, Pan [1 ,2 ]
机构
[1] Shaanxi Normal Univ, Natl Engn Lab Resource Dev Endangered Chinese Cru, Key Lab Med Resources & Nat Pharmaceut Chem, Minist Educ,Coll Life Sci, Xian, Shaanxi, Peoples R China
[2] Chinese Univ Hong Kong, Fac Med, Sch Chinese Med, Shatin, Hong Kong, Peoples R China
[3] Blood Ctr Xian, Xian, Shaanxi, Peoples R China
基金
中国博士后科学基金;
关键词
Sonodynamic therapy; PpIX; Leukemia HL-60 cells; Apoptosis; SARCOMA-180; CELLS; HEMATOPORPHYRIN; ULTRASOUND; DIFFERENTIATION; SONOSENSITIZER; HEPATOMA-22; ATX-70; DAMAGE; LINE;
D O I
10.4149/gpb_2015051
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sono dynamic therapy (SDT) is expected to be a novel therapeutic strategy for tumor. The protoporphyrin IX disodium salt (PpIX), a photosensitizer, can be activated by ultrasound. The present study aims to investigate apoptosis of HL-60 cells induced by PpIX-mediated SDT. 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay was adopted to examine cell toxicity. Apoptosis was detected using Annexin V-PE/7-amino-actinomycin D (7-AAD) double staining. Detection of apoptotic bodies was examined by Hoechst33342 (HO) staining. Western blotting was used to analyze the protein of caspase-3 and poly ADP-ribose polymerase (PARP). Intracellular reactive oxygen species (ROS) was detected by a flow cytometer after exposures. Compared with PpIX alone and ultrasound alone groups, the synergistic cytotoxicity of PpIX plus ultrasound were significantly boosted. In addition, as determined by Annexin V-PE/7-AAD staining, SDT significantly induced HL-60 cell apoptosis, the obvious nuclear condensation was also found with HO staining at 4 hours post-SDT treatment. Furthermore, Western blotting showed visible enhancement of caspase-3 and PARP cleavage in this process. Besides, intracellular ROS production was significantly enhanced after SDT. Our findings demonstrate that PpIX-mediated SDT could induce apoptosis on HL-60 cells, suggesting that apoptosis is an important mechanism of cell death induced by PpIX-mediated SDT.
引用
收藏
页码:155 / 164
页数:10
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