Cargando…

Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model

A hybrid blood–brain barrier (BBB)-on-chip cell culture device is proposed in this study by integrating microcontact printing and perfusion co-culture to facilitate the study of BBB function under high biological fidelity. This is achieved by crosslinking brain extracellular matrix (ECM) proteins to...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Ajay Vikram, Chandrasekar, Vaisali, Laux, Peter, Luch, Andreas, Dakua, Sarada Prasad, Zamboni, Paolo, Shelar, Amruta, Yang, Yin, Pandit, Vaibhav, Tisato, Veronica, Gemmati, Donato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497163/
https://www.ncbi.nlm.nih.gov/pubmed/36139383
http://dx.doi.org/10.3390/cells11182801
_version_ 1784794446506754048
author Singh, Ajay Vikram
Chandrasekar, Vaisali
Laux, Peter
Luch, Andreas
Dakua, Sarada Prasad
Zamboni, Paolo
Shelar, Amruta
Yang, Yin
Pandit, Vaibhav
Tisato, Veronica
Gemmati, Donato
author_facet Singh, Ajay Vikram
Chandrasekar, Vaisali
Laux, Peter
Luch, Andreas
Dakua, Sarada Prasad
Zamboni, Paolo
Shelar, Amruta
Yang, Yin
Pandit, Vaibhav
Tisato, Veronica
Gemmati, Donato
author_sort Singh, Ajay Vikram
collection PubMed
description A hybrid blood–brain barrier (BBB)-on-chip cell culture device is proposed in this study by integrating microcontact printing and perfusion co-culture to facilitate the study of BBB function under high biological fidelity. This is achieved by crosslinking brain extracellular matrix (ECM) proteins to the transwell membrane at the luminal surface and adapting inlet–outlet perfusion on the porous transwell wall. While investigating the anatomical hallmarks of the BBB, tight junction proteins revealed tortuous zonula occludens (ZO-1), and claudin expressions with increased interdigitation in the presence of astrocytes were recorded. Enhanced adherent junctions were also observed. This junctional phenotype reflects in-vivo-like features related to the jamming of cell borders to prevent paracellular transport. Biochemical regulation of BBB function by astrocytes was noted by the transient intracellular calcium effluxes induced into endothelial cells. Geometry-force control of astrocyte–endothelial cell interactions was studied utilizing traction force microscopy (TFM) with fluorescent beads incorporated into a micropatterned polyacrylamide gel (PAG). We observed the directionality and enhanced magnitude in the traction forces in the presence of astrocytes. In the future, we envisage studying transendothelial electrical resistance (TEER) and the effect of chemomechanical stimulations on drug/ligand permeability and transport. The BBB-on-chip model presented in this proposal should serve as an in vitro surrogate to recapitulate the complexities of the native BBB cellular milieus.
format Online
Article
Text
id pubmed-9497163
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-94971632022-09-23 Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model Singh, Ajay Vikram Chandrasekar, Vaisali Laux, Peter Luch, Andreas Dakua, Sarada Prasad Zamboni, Paolo Shelar, Amruta Yang, Yin Pandit, Vaibhav Tisato, Veronica Gemmati, Donato Cells Article A hybrid blood–brain barrier (BBB)-on-chip cell culture device is proposed in this study by integrating microcontact printing and perfusion co-culture to facilitate the study of BBB function under high biological fidelity. This is achieved by crosslinking brain extracellular matrix (ECM) proteins to the transwell membrane at the luminal surface and adapting inlet–outlet perfusion on the porous transwell wall. While investigating the anatomical hallmarks of the BBB, tight junction proteins revealed tortuous zonula occludens (ZO-1), and claudin expressions with increased interdigitation in the presence of astrocytes were recorded. Enhanced adherent junctions were also observed. This junctional phenotype reflects in-vivo-like features related to the jamming of cell borders to prevent paracellular transport. Biochemical regulation of BBB function by astrocytes was noted by the transient intracellular calcium effluxes induced into endothelial cells. Geometry-force control of astrocyte–endothelial cell interactions was studied utilizing traction force microscopy (TFM) with fluorescent beads incorporated into a micropatterned polyacrylamide gel (PAG). We observed the directionality and enhanced magnitude in the traction forces in the presence of astrocytes. In the future, we envisage studying transendothelial electrical resistance (TEER) and the effect of chemomechanical stimulations on drug/ligand permeability and transport. The BBB-on-chip model presented in this proposal should serve as an in vitro surrogate to recapitulate the complexities of the native BBB cellular milieus. MDPI 2022-09-08 /pmc/articles/PMC9497163/ /pubmed/36139383 http://dx.doi.org/10.3390/cells11182801 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Singh, Ajay Vikram
Chandrasekar, Vaisali
Laux, Peter
Luch, Andreas
Dakua, Sarada Prasad
Zamboni, Paolo
Shelar, Amruta
Yang, Yin
Pandit, Vaibhav
Tisato, Veronica
Gemmati, Donato
Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model
title Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model
title_full Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model
title_fullStr Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model
title_full_unstemmed Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model
title_short Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model
title_sort micropatterned neurovascular interface to mimic the blood–brain barrier’s neurophysiology and micromechanical function: a bbb-on-chip model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497163/
https://www.ncbi.nlm.nih.gov/pubmed/36139383
http://dx.doi.org/10.3390/cells11182801
work_keys_str_mv AT singhajayvikram micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT chandrasekarvaisali micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT lauxpeter micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT luchandreas micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT dakuasaradaprasad micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT zambonipaolo micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT shelaramruta micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT yangyin micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT panditvaibhav micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT tisatoveronica micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel
AT gemmatidonato micropatternedneurovascularinterfacetomimicthebloodbrainbarriersneurophysiologyandmicromechanicalfunctionabbbonchipmodel