Cargando…
3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults
Blood‐brain‐barrier (BBB) disruption has been associated with a variety of central‐nervous‐system diseases. In vitro BBB models enable to investigate how the barrier reacts to external injury events, commonly referred to as insults. Here, a human‐cell‐based BBB platform with integrated, transparent...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104638/ https://www.ncbi.nlm.nih.gov/pubmed/36782313 http://dx.doi.org/10.1002/advs.202205752 |
_version_ | 1785026078584078336 |
---|---|
author | Wei, Wei Cardes, Fernando Hierlemann, Andreas Modena, Mario M. |
author_facet | Wei, Wei Cardes, Fernando Hierlemann, Andreas Modena, Mario M. |
author_sort | Wei, Wei |
collection | PubMed |
description | Blood‐brain‐barrier (BBB) disruption has been associated with a variety of central‐nervous‐system diseases. In vitro BBB models enable to investigate how the barrier reacts to external injury events, commonly referred to as insults. Here, a human‐cell‐based BBB platform with integrated, transparent electrodes to monitor barrier tightness in real time at high resolution is presented. The BBB model includes human cerebral endothelial cells and primary pericytes and astrocytes in a 3D arrangement within a pump‐free, open‐microfluidic platform. With this platform, this study demonstrates that oxygen‐glucose deprivation (OGD), which mimics the characteristics of an ischemic insult, induces a rapid remodeling of the cellular actin structures and subsequent morphological changes in the endothelial cells. High‐resolution live imaging shows the formation of large actin stress‐fiber bundles in the endothelial layer during OGD application, which ultimately leads to cell shrinkage and barrier breakage. Simultaneous electrical measurements evidence a rapid decrease of the barrier electrical resistance before the appearance of stress fibers, which indicates that the barrier function is compromised already before the appearance of drastic morphological changes. The results demonstrate that the BBB platform recapitulates the main barrier functions in vitro and can be used to investigate rapid reorganization of the BBB upon application of external stimuli. |
format | Online Article Text |
id | pubmed-10104638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101046382023-04-15 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults Wei, Wei Cardes, Fernando Hierlemann, Andreas Modena, Mario M. Adv Sci (Weinh) Research Articles Blood‐brain‐barrier (BBB) disruption has been associated with a variety of central‐nervous‐system diseases. In vitro BBB models enable to investigate how the barrier reacts to external injury events, commonly referred to as insults. Here, a human‐cell‐based BBB platform with integrated, transparent electrodes to monitor barrier tightness in real time at high resolution is presented. The BBB model includes human cerebral endothelial cells and primary pericytes and astrocytes in a 3D arrangement within a pump‐free, open‐microfluidic platform. With this platform, this study demonstrates that oxygen‐glucose deprivation (OGD), which mimics the characteristics of an ischemic insult, induces a rapid remodeling of the cellular actin structures and subsequent morphological changes in the endothelial cells. High‐resolution live imaging shows the formation of large actin stress‐fiber bundles in the endothelial layer during OGD application, which ultimately leads to cell shrinkage and barrier breakage. Simultaneous electrical measurements evidence a rapid decrease of the barrier electrical resistance before the appearance of stress fibers, which indicates that the barrier function is compromised already before the appearance of drastic morphological changes. The results demonstrate that the BBB platform recapitulates the main barrier functions in vitro and can be used to investigate rapid reorganization of the BBB upon application of external stimuli. John Wiley and Sons Inc. 2023-02-13 /pmc/articles/PMC10104638/ /pubmed/36782313 http://dx.doi.org/10.1002/advs.202205752 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wei, Wei Cardes, Fernando Hierlemann, Andreas Modena, Mario M. 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults |
title | 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults |
title_full | 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults |
title_fullStr | 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults |
title_full_unstemmed | 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults |
title_short | 3D In Vitro Blood‐Brain‐Barrier Model for Investigating Barrier Insults |
title_sort | 3d in vitro blood‐brain‐barrier model for investigating barrier insults |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104638/ https://www.ncbi.nlm.nih.gov/pubmed/36782313 http://dx.doi.org/10.1002/advs.202205752 |
work_keys_str_mv | AT weiwei 3dinvitrobloodbrainbarriermodelforinvestigatingbarrierinsults AT cardesfernando 3dinvitrobloodbrainbarriermodelforinvestigatingbarrierinsults AT hierlemannandreas 3dinvitrobloodbrainbarriermodelforinvestigatingbarrierinsults AT modenamariom 3dinvitrobloodbrainbarriermodelforinvestigatingbarrierinsults |