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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AIP Publishing LLC
2022
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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. |
format | Online Article Text |
id | pubmed-8912992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AIP Publishing LLC |
record_format | MEDLINE/PubMed |
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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