Light-Induced Self-Escape of Spherical Nucleic Acid from Endo/Lysosome for Efficient Non-Cationic Gene Delivery

被引:119
作者
Shi, Leilei [1 ]
Wu, Wenbo [1 ]
Duan, Yukun [1 ]
Xu, Li [2 ]
Xu, Yingying [4 ]
Hou, Lidan [3 ]
Meng, Xiangjun [3 ]
Zhu, Xinyuan [2 ]
Liu, Bin [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, 4 Engn Dr 4, Singapore 117585, Singapore
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Dept Gastroenterol, 639 Zhizaoju Rd, Shanghai 200011, Peoples R China
[4] Fujian Med Univ, Sch Pharm, Dept Pharmaceut, Fuzhou 350108, Peoples R China
基金
新加坡国家研究基金会;
关键词
O-1(2); AIE photosensitizers; antisense oligonucleotides; endosome; lysosome escape; spherical nucleic acid (SNA); AGGREGATION-INDUCED EMISSION; NANOPARTICLES; THERAPY; CANCER; BCL-2; RESISTANCE; OVERCOME; VECTORS;
D O I
10.1002/anie.202006890
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing non-cationic gene carriers and achieving efficient endo/lysosome escape of functional nucleic acids in cytosol are two major challenges faced by the field of gene delivery. Herein, we demonstrate the concept of self-escape spherical nucleic acid (SNA) to achieve light controlled non-cationic gene delivery with sufficient endo/lysosome escape capacity. In this system, Bcl-2 antisense oligonucleotides (OSAs) were conjugated onto the surface of aggregation-induced emission (AIE) photosensitizer (PS) nanoparticles to form core-shell SNA. Once the SNAs were taken up by tumor cells, and upon light irradiation, the accumulative(1)O(2)produced by the AIE PSs ruptured the lysosome structure to promote OSA escape. Prominent in vitro and in vivo results revealed that the AIE-based core-shell SNA could downregulate the anti-apoptosis protein (Bcl-2) and induce tumor cell apoptosis without any transfection reagent.
引用
收藏
页码:19168 / 19174
页数:7
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