Transformation of Cell-Derived Microparticles into Quantum-Dot-Labeled Nanovectors for Antitumor siRNA Delivery

被引:91
作者
Chen, Gang [1 ,2 ,3 ,4 ]
Zhu, Jun-Yi [3 ,4 ]
Zhang, Zhi-Ling [1 ,2 ]
Zhang, Wei [3 ,4 ]
Ren, Jian-Gang [3 ,4 ]
Wu, Min [1 ,2 ]
Hong, Zheng-Yuan [1 ,2 ]
Lv, Cheng [1 ,2 ]
Pang, Dai-Wen [1 ,2 ]
Zhao, Yi-Fang [3 ,4 ]
机构
[1] Wuhan Univ, Key Lab Analyt Chem Biol & Med, Minist Educ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Inst Adv Studies, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Key Lab Oral Biomed, Minist Educ, Wuhan 430079, Peoples R China
[4] Wuhan Univ, Dept Oral & Maxillofacial Surg, Sch & Hosp Stomatol, Wuhan 430079, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
biogenic vesicles; cell-derived microparticles; nanoparticles; quantum dots; targeted delivery; VIRUS;
D O I
10.1002/anie.201410223
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cell-derived microparticles (MPs) have been recently recognized as critical intercellular information conveyors. However, further understanding of their biological behavior and potential application has been hampered by the limitations of current labeling techniques. Herein, a universal donor-cell-assisted membrane biotinylation strategy was proposed for labeling MPs by skillfully utilizing the natural membrane phospholipid exchange of their donor cells. This innovative strategy conveniently led to specific, efficient, reproducible, and biocompatible quantum dot (QD) labeling of MPs, thereby reliably conferring valuable traceability on MPs. By further loading with small interference RNA, QD-labeled MPs that had inherent cell-targeting and biomolecule-conveying ability were successfully employed for combined bioimaging and tumor-targeted therapy. This study provides the first reliable and biofriendly strategy for transforming biogenic MPs into functionalized nanovectors.
引用
收藏
页码:1036 / 1040
页数:5
相关论文
共 18 条
[11]   Cell-derived vesicles as a bioplatform for the encapsulation of theranostic nanomaterials [J].
Silva, Amanda K. Andriola ;
Di Corato, Riccardo ;
Pellegrino, Teresa ;
Chat, Sophie ;
Pugliese, Giammarino ;
Luciani, Nathalie ;
Gazeau, Florence ;
Wilhelm, Claire .
NANOSCALE, 2013, 5 (23) :11374-11384
[12]   Targeting the Tumor Microenvironment for Cancer Therapy [J].
Sounni, Nor Eddine ;
Noel, Agnes .
CLINICAL CHEMISTRY, 2013, 59 (01) :85-93
[13]   Delivery of chemotherapeutic drugs in tumour cell-derived microparticles [J].
Tang, Ke ;
Zhang, Yi ;
Zhang, Huafeng ;
Xu, Pingwei ;
Liu, Jing ;
Ma, Jingwei ;
Lv, Meng ;
Li, Dapeng ;
Katirai, Foad ;
Shen, Guan-Xin ;
Zhang, Guimei ;
Feng, Zuo-Hua ;
Ye, Duyun ;
Huang, Bo .
NATURE COMMUNICATIONS, 2012, 3
[14]   Anti-angiogenic effects of resveratrol mediated by decreased VEGF and increased TSP1 expression in melanoma-endothelial cell co-culture [J].
Trapp, Valerie ;
Parmakhtiar, Basmina ;
Papazian, Vartan ;
Willmott, Lyndsay ;
Fruehauf, John P. .
ANGIOGENESIS, 2010, 13 (04) :305-315
[15]  
van der Heyde HC, 2011, METHODS MOL BIOL, V699, P337, DOI 10.1007/978-1-61737-950-5_16
[16]   Quick-Response Magnetic Nanospheres for Rapid, Efficient Capture and Sensitive Detection of Circulating Tumor Cells [J].
Wen, Cong-Ying ;
Wu, Ling-Ling ;
Zhang, Zhi-Ling ;
Liu, Yu-Lin ;
Wei, Shao-Zhong ;
Hu, Jiao ;
Tang, Man ;
Sun, En-Ze ;
Gong, Yi-Ping ;
Yu, Jing ;
Pang, Dai-Wen .
ACS NANO, 2014, 8 (01) :941-949
[17]   Labeling the nucleocapsid of enveloped baculovirus with quantum dots for single-virus tracking [J].
Wen, Li ;
Lin, Yi ;
Zheng, Zhen-Hua ;
Zhang, Zhi-Ling ;
Zhang, Li-Juan ;
Wang, Li-Ying ;
Wang, Han-Zhong ;
Pang, Dai-Wen .
BIOMATERIALS, 2014, 35 (07) :2295-2301
[18]   Microvesicle-mediated delivery of transforming growth factor β1 siRNA for the suppression of tumor growth in mice [J].
Zhang, Yaqin ;
Li, Limin ;
Yu, Jianxiong ;
Zhu, Dihan ;
Zhang, Yujing ;
Li, Xihan ;
Gu, Hongwei ;
Zhang, Chen-Yu ;
Zen, Ke .
BIOMATERIALS, 2014, 35 (14) :4390-4400