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Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro

The blood-brain barrier prevents the entry of many therapeutic agents into the brain. Various nanocarriers have been developed to help agents to cross this barrier, but they all have limitations, with regard to tissue-selectivity and their ability to cross the endothelium. This study investigated th...

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Autores principales: Gromnicova, Radka, Davies, Heather A., Sreekanthreddy, Peddagangannagari, Romero, Ignacio A., Lund, Torben, Roitt, Ivan M., Phillips, James B., Male, David K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855187/
https://www.ncbi.nlm.nih.gov/pubmed/24339894
http://dx.doi.org/10.1371/journal.pone.0081043
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author Gromnicova, Radka
Davies, Heather A.
Sreekanthreddy, Peddagangannagari
Romero, Ignacio A.
Lund, Torben
Roitt, Ivan M.
Phillips, James B.
Male, David K.
author_facet Gromnicova, Radka
Davies, Heather A.
Sreekanthreddy, Peddagangannagari
Romero, Ignacio A.
Lund, Torben
Roitt, Ivan M.
Phillips, James B.
Male, David K.
author_sort Gromnicova, Radka
collection PubMed
description The blood-brain barrier prevents the entry of many therapeutic agents into the brain. Various nanocarriers have been developed to help agents to cross this barrier, but they all have limitations, with regard to tissue-selectivity and their ability to cross the endothelium. This study investigated the potential for 4 nm coated gold nanoparticles to act as selective carriers across human brain endothelium and subsequently to enter astrocytes. The transfer rate of glucose-coated gold nanoparticles across primary human brain endothelium was at least three times faster than across non-brain endothelia. Movement of these nanoparticles occurred across the apical and basal plasma membranes via the cytosol with relatively little vesicular or paracellular migration; antibiotics that interfere with vesicular transport did not block migration. The transfer rate was also dependent on the surface coating of the nanoparticle and incubation temperature. Using a novel 3-dimensional co-culture system, which includes primary human astrocytes and a brain endothelial cell line hCMEC/D3, we demonstrated that the glucose-coated nanoparticles traverse the endothelium, move through the extracellular matrix and localize in astrocytes. The movement of the nanoparticles through the matrix was >10 µm/hour and they appeared in the nuclei of the astrocytes in considerable numbers. These nanoparticles have the correct properties for efficient and selective carriers of therapeutic agents across the blood-brain barrier.
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spelling pubmed-38551872013-12-11 Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro Gromnicova, Radka Davies, Heather A. Sreekanthreddy, Peddagangannagari Romero, Ignacio A. Lund, Torben Roitt, Ivan M. Phillips, James B. Male, David K. PLoS One Research Article The blood-brain barrier prevents the entry of many therapeutic agents into the brain. Various nanocarriers have been developed to help agents to cross this barrier, but they all have limitations, with regard to tissue-selectivity and their ability to cross the endothelium. This study investigated the potential for 4 nm coated gold nanoparticles to act as selective carriers across human brain endothelium and subsequently to enter astrocytes. The transfer rate of glucose-coated gold nanoparticles across primary human brain endothelium was at least three times faster than across non-brain endothelia. Movement of these nanoparticles occurred across the apical and basal plasma membranes via the cytosol with relatively little vesicular or paracellular migration; antibiotics that interfere with vesicular transport did not block migration. The transfer rate was also dependent on the surface coating of the nanoparticle and incubation temperature. Using a novel 3-dimensional co-culture system, which includes primary human astrocytes and a brain endothelial cell line hCMEC/D3, we demonstrated that the glucose-coated nanoparticles traverse the endothelium, move through the extracellular matrix and localize in astrocytes. The movement of the nanoparticles through the matrix was >10 µm/hour and they appeared in the nuclei of the astrocytes in considerable numbers. These nanoparticles have the correct properties for efficient and selective carriers of therapeutic agents across the blood-brain barrier. Public Library of Science 2013-12-05 /pmc/articles/PMC3855187/ /pubmed/24339894 http://dx.doi.org/10.1371/journal.pone.0081043 Text en © 2013 Gromnicova et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gromnicova, Radka
Davies, Heather A.
Sreekanthreddy, Peddagangannagari
Romero, Ignacio A.
Lund, Torben
Roitt, Ivan M.
Phillips, James B.
Male, David K.
Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro
title Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro
title_full Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro
title_fullStr Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro
title_full_unstemmed Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro
title_short Glucose-Coated Gold Nanoparticles Transfer across Human Brain Endothelium and Enter Astrocytes In Vitro
title_sort glucose-coated gold nanoparticles transfer across human brain endothelium and enter astrocytes in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855187/
https://www.ncbi.nlm.nih.gov/pubmed/24339894
http://dx.doi.org/10.1371/journal.pone.0081043
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