| Literature DB >> 29608290 |
Kelong Fan1, Xiaohua Jia2, Meng Zhou1,3, Kun Wang2, João Conde4, Jiuyang He1, Jie Tian2, Xiyun Yan1,3.
Abstract
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.Entities:
Keywords: blood brain barrier; glioma-targeted therapy; human H-ferritin nanocarrier; receptor-mediated transcytosis; transferrin receptor 1
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Year: 2018 PMID: 29608290 DOI: 10.1021/acsnano.7b06969
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881