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Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert

The blood-brain barrier (BBB) is a specialized brain endothelial barrier structure that regulates the highly selective transport of molecules under continuous blood flow. Recently, various types of BBB-on-chip models have been developed to mimic the microenvironmental cues that regulate the human BB...

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Autores principales: Miura, Shigenori, Morimoto, Yuya, Furihata, Tomomi, Takeuchi, Shoji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIP Publishing LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912992/
https://www.ncbi.nlm.nih.gov/pubmed/35308826
http://dx.doi.org/10.1063/5.0085564
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author Miura, Shigenori
Morimoto, Yuya
Furihata, Tomomi
Takeuchi, Shoji
author_facet Miura, Shigenori
Morimoto, Yuya
Furihata, Tomomi
Takeuchi, Shoji
author_sort Miura, Shigenori
collection PubMed
description The blood-brain barrier (BBB) is a specialized brain endothelial barrier structure that regulates the highly selective transport of molecules under continuous blood flow. Recently, various types of BBB-on-chip models have been developed to mimic the microenvironmental cues that regulate the human BBB drug transport. However, technical difficulties in complex microfluidic systems limit their accessibility. Here, we propose a simple and easy-to-handle microfluidic device integrated with a cell culture insert to investigate the functional regulation of the human BBB endothelium in response to fluid shear stress (FSS). Using currently established immortalized human brain microvascular endothelial cells (HBMEC/ci18), we formed a BBB endothelial barrier without the substantial loss of barrier tightness under the relatively low range of FSS (0.1–1 dyn/cm(2)). Expression levels of key BBB transporters and receptors in the HBMEC/ci18 cells were dynamically changed in response to the FSS, and the effect of FSS reached a plateau around 1 dyn/cm(2). Similar responses were observed in the primary HBMECs. Taking advantage of the detachable cell culture insert from the device, the drug efflux activity of P-glycoprotein (P-gp) was analyzed by the bidirectional permeability assay after the perfusion culture of cells. The data revealed that the FSS-stimulated BBB endothelium exhibited the 1.9-fold higher P-gp activity than that of the static culture control. Our microfluidic system coupling with the transwell model provides a functional human BBB endothelium with secured transporter activity, which is useful to investigate the bidirectional transport of drugs and its regulation by FSS.
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spelling pubmed-89129922022-03-17 Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert Miura, Shigenori Morimoto, Yuya Furihata, Tomomi Takeuchi, Shoji APL Bioeng Articles The blood-brain barrier (BBB) is a specialized brain endothelial barrier structure that regulates the highly selective transport of molecules under continuous blood flow. Recently, various types of BBB-on-chip models have been developed to mimic the microenvironmental cues that regulate the human BBB drug transport. However, technical difficulties in complex microfluidic systems limit their accessibility. Here, we propose a simple and easy-to-handle microfluidic device integrated with a cell culture insert to investigate the functional regulation of the human BBB endothelium in response to fluid shear stress (FSS). Using currently established immortalized human brain microvascular endothelial cells (HBMEC/ci18), we formed a BBB endothelial barrier without the substantial loss of barrier tightness under the relatively low range of FSS (0.1–1 dyn/cm(2)). Expression levels of key BBB transporters and receptors in the HBMEC/ci18 cells were dynamically changed in response to the FSS, and the effect of FSS reached a plateau around 1 dyn/cm(2). Similar responses were observed in the primary HBMECs. Taking advantage of the detachable cell culture insert from the device, the drug efflux activity of P-glycoprotein (P-gp) was analyzed by the bidirectional permeability assay after the perfusion culture of cells. The data revealed that the FSS-stimulated BBB endothelium exhibited the 1.9-fold higher P-gp activity than that of the static culture control. Our microfluidic system coupling with the transwell model provides a functional human BBB endothelium with secured transporter activity, which is useful to investigate the bidirectional transport of drugs and its regulation by FSS. AIP Publishing LLC 2022-03-09 /pmc/articles/PMC8912992/ /pubmed/35308826 http://dx.doi.org/10.1063/5.0085564 Text en © 2022 Author(s). https://creativecommons.org/licenses/by/4.0/All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Articles
Miura, Shigenori
Morimoto, Yuya
Furihata, Tomomi
Takeuchi, Shoji
Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
title Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
title_full Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
title_fullStr Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
title_full_unstemmed Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
title_short Functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
title_sort functional analysis of human brain endothelium using a microfluidic device integrating a cell culture insert
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912992/
https://www.ncbi.nlm.nih.gov/pubmed/35308826
http://dx.doi.org/10.1063/5.0085564
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