Ferritin Nanocarrier Traverses the Blood Brain Barrier and Kills Glioma

被引:314
作者
Fan, Kelong [1 ]
Jia, Xiaohua
Zhou, Meng [1 ,3 ]
Wang, Kun [2 ]
Conde, Joao [4 ]
He, Jiuyang [1 ]
Tian, Jie [2 ]
Yan, Xiyun [1 ,3 ]
机构
[1] Chinese Acad Sci, Key Lab Prot & Peptide Pharmaceut, CAS Univ Tokyo Joint Lab Struct Virol & Immunol, Inst Biophys, Beijing 100101, Peoples R China
[2] Chinese Acad Sci, Key Lab Mol Imaging, Inst Automat, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[4] Queen Mary Univ London, Sch Engn & Mat Sci, London E1 4NS, England
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
human H-ferritin nanocarrier; blood brain barrier; transferrin receptor 1; receptor-mediated transcytosis; glioma-targeted therapy; RECEPTOR-MEDIATED ENDOCYTOSIS; TRANSFERRIN RECEPTOR; DRUG-DELIVERY; H-FERRITIN; BINDING-SITES; NANOPARTICLES; GLIOBLASTOMA; TUMORS; PATHWAY; CANCER;
D O I
10.1021/acsnano.7b06969
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Over the last decades, considerable efforts have been put into developing active nanocarrier systems that cross the blood brain barrier (BBB) to treat brain-related diseases such as glioma tumors. However, to date none have been approved for clinical usage. Here, we show that a human H-ferritin (HFn) nanocarrier both successfully crosses the BBB and kills glioma tumor cells. Its principle point of entry is the HFn receptor (transferrin receptor 1), which is overexpressed in both BBB endothelial cells (ECs) and glioma cells. Importantly, we found that HFn enters and exits the BBB via the endosome compartment. In contrast, upon specifically targeting and entering glioma cells, nearly all of the HFn accumulated in the lysosomal compartment, resulting in the killing of glioma tumor cells, with no HFn accumulation in the surrounding healthy brain tissue. Thus, HFn is an ideal nanocarrier for glioma therapy and possesses the potential to serve as a therapeutic approach against a broad range of central nervous system diseases.
引用
收藏
页码:4105 / 4115
页数:11
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