中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Tumor associated macrophage-targeted microRNA delivery with dual-responsive polypeptide nanovectors for anti-cancer therapy

文献类型:期刊论文

作者Lanlan Liu; Huqiang Yi; Huamei He; Hong Pan; Lintao Cai; Yifan Ma
刊名Biomaterials
出版日期2017
文献子类期刊论文
英文摘要Repolarizing Tumor-associated macrophages (TAMs) to anti-tumor M1 macrophages with microRNA (miR) is a plausible approach for cancer treatment. However, how to achieve TAM-targeted miR delivery remains a challenge. The present study generated redox/pH dual-responsive hybrid polypeptide nanovectors, which consisted of self-crosslinked redox-responsive nanoparticles based on galactose-functionalized n-butylamine-poly(l-lysine)-b-poly(l-cysteine) polypeptides (GLC) coated with DCA-grafted sheddable PEG-PLL (sPEG) copolymers. The ex vivo study showed that sPEG shielded cationic GLC core at physiological pH but quickly shed off to re-expose GLC due to it charge reversible property. Encapsulation with sPEG/GLC nanovectors effectively facilitated macrophage-targeted miR delivery at the acidic condition but diminished miR uptake at neutral pH. Administration of miR155-loaded sPEG/GLC (sPEG/GLC/155) nanocomplexes increased miR155 expression in TAMs about 100–400 folds both in vitro and in vivo. sPEG/GLC/155 also effectively repolarized immunosuppressive TAMs to anti-tumor M1 macrophages through elevating M1 macrophage markers (IL-12, iNOS, MHC II) and suppressing M2 macrophage markers (Msr2 and Arg1) in TAMs. Moreover, the treatment of sPEG/GLC/155 significantly increased activated T lymphocytes and NK cells in tumors, which consequently led to robust tumor regression. Hence, TAM-targeted delivery of miR with redox/pH dual-responsive sPEG/GLC nanovectors could be a promising approach to re-polarize TAMs to M1 macrophages in situ and induce tumor regression.
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语种英语
源URL[http://ir.siat.ac.cn:8080/handle/172644/12258]  
专题深圳先进技术研究院_医药所
作者单位Biomaterials
推荐引用方式
GB/T 7714
Lanlan Liu,Huqiang Yi,Huamei He,et al. Tumor associated macrophage-targeted microRNA delivery with dual-responsive polypeptide nanovectors for anti-cancer therapy[J]. Biomaterials,2017.
APA Lanlan Liu,Huqiang Yi,Huamei He,Hong Pan,Lintao Cai,&Yifan Ma.(2017).Tumor associated macrophage-targeted microRNA delivery with dual-responsive polypeptide nanovectors for anti-cancer therapy.Biomaterials.
MLA Lanlan Liu,et al."Tumor associated macrophage-targeted microRNA delivery with dual-responsive polypeptide nanovectors for anti-cancer therapy".Biomaterials (2017).

入库方式: OAI收割

来源:深圳先进技术研究院

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