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Dual Channel Microfluidics for Mimicking the Blood–Brain Barrier
[Image: see text] High-resolution imaging is essential for analysis of the steps and way stations of cargo transport in in vitro models of the endothelium. In this study, we demonstrate a microfluidic system consisting of two channels horizontally separated by a cell-growth-promoting membrane. Its d...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905877/ https://www.ncbi.nlm.nih.gov/pubmed/33480670 http://dx.doi.org/10.1021/acsnano.0c09263 |
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author | Buchroithner, Boris Mayr, Sandra Hauser, Fabian Priglinger, Eleni Stangl, Herbert Santa-Maria, Ana Raquel Deli, Maria A. Der, Andras Klar, Thomas A. Axmann, Markus Sivun, Dmitry Mairhofer, Mario Jacak, Jaroslaw |
author_facet | Buchroithner, Boris Mayr, Sandra Hauser, Fabian Priglinger, Eleni Stangl, Herbert Santa-Maria, Ana Raquel Deli, Maria A. Der, Andras Klar, Thomas A. Axmann, Markus Sivun, Dmitry Mairhofer, Mario Jacak, Jaroslaw |
author_sort | Buchroithner, Boris |
collection | PubMed |
description | [Image: see text] High-resolution imaging is essential for analysis of the steps and way stations of cargo transport in in vitro models of the endothelium. In this study, we demonstrate a microfluidic system consisting of two channels horizontally separated by a cell-growth-promoting membrane. Its design allows for high-resolution (down to single-molecule level) imaging using a high numerical aperture objective with a short working distance. To reduce optical aberrations and enable single-molecule-sensitive imaging, an observation window was constructed in the membrane via laser cutting with subsequent structuring using 3D multiphoton lithography for improved cell growth. The upper channel was loaded with endothelial cells under flow conditions, which showed polarization and junction formation. A coculture of human vascular endothelial cells with pericytes was developed that mimics the blood–brain barrier. Finally, this dual channel microfluidics system enabled 3D localization microscopy of the cytoskeleton and 3D single-molecule-sensitive tracing of lipoprotein particles. |
format | Online Article Text |
id | pubmed-7905877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79058772021-02-25 Dual Channel Microfluidics for Mimicking the Blood–Brain Barrier Buchroithner, Boris Mayr, Sandra Hauser, Fabian Priglinger, Eleni Stangl, Herbert Santa-Maria, Ana Raquel Deli, Maria A. Der, Andras Klar, Thomas A. Axmann, Markus Sivun, Dmitry Mairhofer, Mario Jacak, Jaroslaw ACS Nano [Image: see text] High-resolution imaging is essential for analysis of the steps and way stations of cargo transport in in vitro models of the endothelium. In this study, we demonstrate a microfluidic system consisting of two channels horizontally separated by a cell-growth-promoting membrane. Its design allows for high-resolution (down to single-molecule level) imaging using a high numerical aperture objective with a short working distance. To reduce optical aberrations and enable single-molecule-sensitive imaging, an observation window was constructed in the membrane via laser cutting with subsequent structuring using 3D multiphoton lithography for improved cell growth. The upper channel was loaded with endothelial cells under flow conditions, which showed polarization and junction formation. A coculture of human vascular endothelial cells with pericytes was developed that mimics the blood–brain barrier. Finally, this dual channel microfluidics system enabled 3D localization microscopy of the cytoskeleton and 3D single-molecule-sensitive tracing of lipoprotein particles. American Chemical Society 2021-01-22 2021-02-23 /pmc/articles/PMC7905877/ /pubmed/33480670 http://dx.doi.org/10.1021/acsnano.0c09263 Text en © 2021 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Buchroithner, Boris Mayr, Sandra Hauser, Fabian Priglinger, Eleni Stangl, Herbert Santa-Maria, Ana Raquel Deli, Maria A. Der, Andras Klar, Thomas A. Axmann, Markus Sivun, Dmitry Mairhofer, Mario Jacak, Jaroslaw Dual Channel Microfluidics for Mimicking the Blood–Brain Barrier |
title | Dual Channel Microfluidics for Mimicking the Blood–Brain
Barrier |
title_full | Dual Channel Microfluidics for Mimicking the Blood–Brain
Barrier |
title_fullStr | Dual Channel Microfluidics for Mimicking the Blood–Brain
Barrier |
title_full_unstemmed | Dual Channel Microfluidics for Mimicking the Blood–Brain
Barrier |
title_short | Dual Channel Microfluidics for Mimicking the Blood–Brain
Barrier |
title_sort | dual channel microfluidics for mimicking the blood–brain
barrier |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905877/ https://www.ncbi.nlm.nih.gov/pubmed/33480670 http://dx.doi.org/10.1021/acsnano.0c09263 |
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