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Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy
BACKGROUND: Ferritin, the natural iron storage protein complex, self-assembles into a uniform cage-like structure. Human H-ferritin (HFn) has been shown to transverse the blood–brain barrier (BBB) by binding to transferrin receptor 1 (TfR1), which is abundant in endothelial cells and overexpressed i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201891/ https://www.ncbi.nlm.nih.gov/pubmed/34120610 http://dx.doi.org/10.1186/s12951-021-00925-1 |
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author | Huang, Chiun-Wei Chuang, Chia-Pao Chen, Yan-Jun Wang, Hsu-Yuan Lin, Jia-Jia Huang, Chiung-Yin Wei, Kuo-Chen Huang, Feng-Ting |
author_facet | Huang, Chiun-Wei Chuang, Chia-Pao Chen, Yan-Jun Wang, Hsu-Yuan Lin, Jia-Jia Huang, Chiung-Yin Wei, Kuo-Chen Huang, Feng-Ting |
author_sort | Huang, Chiun-Wei |
collection | PubMed |
description | BACKGROUND: Ferritin, the natural iron storage protein complex, self-assembles into a uniform cage-like structure. Human H-ferritin (HFn) has been shown to transverse the blood–brain barrier (BBB) by binding to transferrin receptor 1 (TfR1), which is abundant in endothelial cells and overexpressed in tumors, and enters cells via endocytosis. Ferritin is easily genetically modified with various functional molecules, justifying that it possesses great potential for development into a nanocarrier drug delivery system. RESULTS: In this study, a unique integrin α2β1-targeting H-ferritin (2D-HFn)-based drug delivery system was developed that highlights the feasibility of receptor-mediated transcytosis (RMT) for glioma tumor treatment. The integrin targeting α2β1 specificity was validated by biolayer interferometry in real time monitoring and followed by cell binding, chemo-drug encapsulation stability studies. Compared with naïve HFn, 2D-HFn dramatically elevated not only doxorubicin (DOX) drug loading capacity (up to 458 drug molecules/protein cage) but also tumor targeting capability after crossing BBB in an in vitro transcytosis assay (twofold) and an in vivo orthotopic glioma model. Most importantly, DOX-loaded 2D-HFn significantly suppressed subcutaneous and orthotopic U-87MG tumor progression; in particular, orthotopic glioma mice survived for more than 80 days. CONCLUSIONS: We believe that this versatile nanoparticle has established a proof-of-concept platform to enable more accurate brain tumor targeting and precision treatment arrangements. Additionally, this unique RMT based ferritin drug delivery technique would accelerate the clinical development of an innovative drug delivery strategy for central nervous system diseases with limited side effects in translational medicine. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00925-1. |
format | Online Article Text |
id | pubmed-8201891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82018912021-06-16 Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy Huang, Chiun-Wei Chuang, Chia-Pao Chen, Yan-Jun Wang, Hsu-Yuan Lin, Jia-Jia Huang, Chiung-Yin Wei, Kuo-Chen Huang, Feng-Ting J Nanobiotechnology Research BACKGROUND: Ferritin, the natural iron storage protein complex, self-assembles into a uniform cage-like structure. Human H-ferritin (HFn) has been shown to transverse the blood–brain barrier (BBB) by binding to transferrin receptor 1 (TfR1), which is abundant in endothelial cells and overexpressed in tumors, and enters cells via endocytosis. Ferritin is easily genetically modified with various functional molecules, justifying that it possesses great potential for development into a nanocarrier drug delivery system. RESULTS: In this study, a unique integrin α2β1-targeting H-ferritin (2D-HFn)-based drug delivery system was developed that highlights the feasibility of receptor-mediated transcytosis (RMT) for glioma tumor treatment. The integrin targeting α2β1 specificity was validated by biolayer interferometry in real time monitoring and followed by cell binding, chemo-drug encapsulation stability studies. Compared with naïve HFn, 2D-HFn dramatically elevated not only doxorubicin (DOX) drug loading capacity (up to 458 drug molecules/protein cage) but also tumor targeting capability after crossing BBB in an in vitro transcytosis assay (twofold) and an in vivo orthotopic glioma model. Most importantly, DOX-loaded 2D-HFn significantly suppressed subcutaneous and orthotopic U-87MG tumor progression; in particular, orthotopic glioma mice survived for more than 80 days. CONCLUSIONS: We believe that this versatile nanoparticle has established a proof-of-concept platform to enable more accurate brain tumor targeting and precision treatment arrangements. Additionally, this unique RMT based ferritin drug delivery technique would accelerate the clinical development of an innovative drug delivery strategy for central nervous system diseases with limited side effects in translational medicine. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00925-1. BioMed Central 2021-06-13 /pmc/articles/PMC8201891/ /pubmed/34120610 http://dx.doi.org/10.1186/s12951-021-00925-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Huang, Chiun-Wei Chuang, Chia-Pao Chen, Yan-Jun Wang, Hsu-Yuan Lin, Jia-Jia Huang, Chiung-Yin Wei, Kuo-Chen Huang, Feng-Ting Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
title | Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
title_full | Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
title_fullStr | Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
title_full_unstemmed | Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
title_short | Integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
title_sort | integrin α(2)β(1)-targeting ferritin nanocarrier traverses the blood–brain barrier for effective glioma chemotherapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201891/ https://www.ncbi.nlm.nih.gov/pubmed/34120610 http://dx.doi.org/10.1186/s12951-021-00925-1 |
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