Activatable Ferritin Nanocomplex for Real-Time Monitoring of Caspase-3 Activation during Photodynamic Therapy

被引:40
作者
Wang, Jingjing [1 ,2 ]
Zhang, Liwen [1 ,2 ]
Chen, Minglong [3 ]
Gao, Shi [3 ]
Zhu, Lei [1 ,2 ]
机构
[1] Xiamen Univ, Sch Publ Hlth, State Key Lab Mol Vaccinol & Mol Diagnost, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Sch Publ Hlth, Ctr Mol Imaging & Translat Med, Xiamen 361005, Peoples R China
[3] Jilin Univ, China Japan Union Hosp, Changchun 130033, Peoples R China
基金
美国国家科学基金会; 国家高技术研究发展计划(863计划);
关键词
photodynamic therapy; apoptosis; caspase-3; activatable probe; ferritin; IN APOPTOSIS SENSOR; SINGLET OXYGEN; TRANSFERRIN RECEPTORS; CELL; TUMORS; AGENT; PHOTOSENSITIZATION; NANOPARTICLES; EFFICIENT; CASCADE;
D O I
10.1021/acsami.5b07316
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
One mechanism of photodynamic therapy (PDT) for the ablation of tumors is to induce apoptosis. Visualization of apoptosis during PDT in real-time is of great benefit for predicting and evaluating therapeutic outcomes. Herein, we engineered a highly stable and sensitive caspase-3 ferritin activatable probe (FABP/ZnPc) for simultaneous delivery of a photosensitizer (ZnPc) and real-time visualization of apoptosis during PDT. Upon near-infrared (NIR) light irradiation, ZnPc becomes active and initiates apoptosis, upon which the outer layer of the FABP/ZnPc is degraded by the apoptotic marker, caspase-3, to boost strong fluorescent signals, ultimately allowing real-time imaging of apoptosis. Our results demonstrate the utility of FABP/ZnPc as a tool for PDT and simultaneous imaging of caspase-3 activation in vitro and in vivo. Overall, the ability of FABP/ZnPc to image apoptosis during PDT will not only facilitate optimizing and personalizing the PDT strategy but is also important for understanding the mechanisms of PDT.
引用
收藏
页码:23248 / 23256
页数:9
相关论文
共 49 条
[31]   Infrared laser pulse triggers increased singlet oxygen production in tumour cells [J].
Sokolovski, S. G. ;
Zolotovskaya, S. A. ;
Goltsov, A. ;
Pourreyron, C. ;
South, A. P. ;
Rafailov, E. U. .
SCIENTIFIC REPORTS, 2013, 3
[32]  
Stefflova K, 2007, CURR MED CHEM, V14, P2110
[33]   Targeted photodynamic therapy agent with a built-in apoptosis sensor for in vivo near-infrared imaging of tumor apoptosis triggered by its photosensitization in situ [J].
Stefflova, Klara ;
Chen, Juan ;
Li, Hui ;
Zheng, Gang .
MOLECULAR IMAGING, 2006, 5 (04) :520-532
[34]   Photodynamic therapy agent with a built-in apoptosis sensor for evaluating its own therapeutic outcome in situ [J].
Stefflova, Klara ;
Chen, Juan ;
Marotta, Diane ;
Li, Hui ;
Zheng, Gang .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (13) :3850-3856
[35]   Antitumor Effects in Gastrointestinal Stromal Tumors Using Photodynamic Therapy with a Novel Glucose-Conjugated Chlorin [J].
Tanaka, Mamoru ;
Kataoka, Hiromi ;
Yano, Shigenobu ;
Ohi, Hiromi ;
Moriwaki, Kazuhiro ;
Akashi, Haruo ;
Taguchi, Takahiro ;
Hayashi, Noriyuki ;
Hamano, Shingo ;
Mori, Yoshinori ;
Kubota, Eiji ;
Tanida, Satoshi ;
Joh, Takashi .
MOLECULAR CANCER THERAPEUTICS, 2014, 13 (04) :767-775
[36]   Cell-Specific and pH-Activatable Rubyrin-Loaded Nanoparticles for Highly Selective Near-Infrared Photodynamic Therapy against Cancer [J].
Tian, Jiangwei ;
Ding, Lin ;
Xu, Hai-Jun ;
Shen, Zhen ;
Ju, Huangxian ;
Jia, Li ;
Bao, Lei ;
Yu, Jun-Sheng .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (50) :18850-18858
[37]  
Uzdensky AB, 2002, PHOTOCHEM PHOTOBIOL, V76, P320, DOI 10.1562/0031-8655(2002)076<0320:POHBTH>2.0.CO
[38]  
2
[39]   Discovery of a Highly Selective Caspase-3 Substrate for Imaging Live Cells [J].
Vickers, Chris J. ;
Gonzalez-Paez, Gonzalo E. ;
Wolan, Dennis W. .
ACS CHEMICAL BIOLOGY, 2014, 9 (10) :2199-2203
[40]   Quantitative analysis of caspase-3 activation by fitting fluorescence emission spectra in living cells [J].
Wang, Longxiang ;
Chen, Tongsheng ;
Qu, Junle ;
Wei, Xunbin .
MICRON, 2009, 40 (08) :811-820