TY - JOUR
T1 - Ferritin Nanocarrier Traverses the Blood Brain Barrier and Kills Glioma
AU - Fan, Kelong
AU - Jia, Xiaohua
AU - Zhou, Meng
AU - Wang, Kun
AU - Conde, João
AU - He, Jiuyang
AU - Tian, Jie
AU - Yan, Xiyun
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/5/22
Y1 - 2018/5/22
N2 - 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.
AB - 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.
KW - blood brain barrier
KW - glioma-targeted therapy
KW - human H-ferritin nanocarrier
KW - receptor-mediated transcytosis
KW - transferrin receptor 1
UR - https://www.scopus.com/pages/publications/85047391665
U2 - 10.1021/acsnano.7b06969
DO - 10.1021/acsnano.7b06969
M3 - 文章
C2 - 29608290
AN - SCOPUS:85047391665
SN - 1936-0851
VL - 12
SP - 4105
EP - 4115
JO - ACS Nano
JF - ACS Nano
IS - 5
ER -