Self-Assembly of Poly-Adenine-Tailed CpG Oligonucleotide-Gold Nanoparticle Nanoconjugates with Immunostimulatory Activity

被引:98
作者
Chen, Nan [1 ,2 ]
Wei, Min [1 ,2 ]
Sun, Yanhong [1 ,2 ]
Li, Fan [1 ,2 ]
Pei, Hao [1 ,2 ]
Li, Xiaoming [1 ,2 ]
Su, Shao [3 ]
He, Yao [4 ,5 ]
Wang, Lianhui [3 ]
Shi, Jiye [6 ]
Fan, Chunhai [1 ,2 ]
Huang, Qing [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, SSRF, Div Phys Biol, Shanghai 201800, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, SSRF, Bioimaging Ctr, Shanghai 201800, Peoples R China
[3] Nanjing Univ Posts & Telecommun, Sch Mat Sci & Engn, IAM, KLOEID, Nanjing 210046, Jiangsu, Peoples R China
[4] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Suzhou 215123, Jiangsu, Peoples R China
[5] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
[6] UCB Pharma, Slough SL1 3WE, Berks, England
基金
中国国家自然科学基金;
关键词
DNA; DELIVERY; OLIGODEOXYNUCLEOTIDES; RECOGNITION; RECEPTOR; BIOLOGY; PHOSPHODIESTER; TLR9; SIZE;
D O I
10.1002/smll.201300903
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic unmethylated cytosine-guanine (CpG) oligodeoxynucleotides (CpG ODNs) possess high immunostimulatory activity and have been widely used as a therapeutic tool for various diseases including infection, allergies, and cancer. A variety of nanocarriers have been developed for intracellular delivery of CpG ODNs that are otherwise nonpermeable through the cellular membrane. For example, previous studies showed that gold nanoparticles (AuNPs) could efficiently deliver synthetic thiolated CpG ODNs into cultured cells and induce expression of proinflammatory cytokines. Nevertheless, the necessity of using thiolated CpG ODNs for the modification of AuNPs inevitably complicates the synthesis of the nanoconjugates and increases the cost. A new approach is demonstrated for facile assembly of AuNP-CpG nanoconjugates for cost-effective drug delivery. It is found that non-thiolated, diblock ODNs containing a CpG motif and a poly-adenine (polyA) tail can readily self-assemble on the surface of AuNPs with controllable and tunable density. Such nanoconjugates are efficiently delivered into RAW264.7 cells and induce immune response in a Toll-like receptor 9 (TLR9)-dependent manner. Under optimal conditions, polyA-CpG-AuNPs show significantly higher immunostimulatory activity than their thiolated counterpart. In addition, the immunostimulatory activity of CpG-AuNPs can be modulated by varying the length of the polyA tail. In vivo induction of immune responses in mice is demonstrated by using polyA-tailed CpG-AuNP nanoconjugates. Non-thiolated, diblock poly-adenine-tailed unmethylated cytosine-guanine (CpG) oligodeoxynucleotides, which self-assemble on the surface of gold nanoparticles (AuNPs) with tightly controlled density, are efficiently delivered into RAW264.7 cells and exhibit high immunostimulatory activity. CpG-AuNP conjugates are capable of inducing an immune response in vivo. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:368 / 375
页数:8
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