Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Establishment of an In Vitro Neurovascular Unit Model With Blood and Brain Components and Investigation of Its Blood–Brain Barrier
Date
2025-11-01
Author
Kole, Gozde E.
KOCAGÖZ, ZÜHTÜ TANIL
Hasırcı, Vasıf Nejat
YÜCEL, DENİZ
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
25
views
0
downloads
Cite This
The neurovascular unit (NVU), including the blood–brain barrier (BBB), governs the interaction between neural tissue and blood vessels. The BBB is a highly selective interface that regulates molecular exchange between the bloodstream and the central nervous system. This study aimed to develop a structurally relevant, multicellular in vitro NVU model integrating both vascular and brain microenvironments to evaluate BBB function. A fibrous membrane mimicking the basement membrane was fabricated via electrospinning, while a methacrylated hyaluronic acid (MeHA)-collagen hydrogel was used on the brain side. Endothelial cells (ECs) were cultured on the vascular side, and astrocytes, pericytes, and neuronal model cells were embedded within the hydrogel. The model was optimized for cell viability and endothelial monolayer formation. Cell behavior was assessed via immunocytochemistry, and barrier function was evaluated using TEER measurements and permeability assays with fluorescein, 0.4 and 20 kDa dextran, ceftriaxone, and amikacin. CD31 expression was elevated in the multicellular model, indicating improved endothelial integrity. The model achieved a TEER of 166.86 ± 5.75 Ω versus 121.70 ± 13.58 Ω cm2 in monoculture. Permeability to tracers was significantly reduced in the multicellular model, and ceftriaxone showed higher transport than amikacin, reflecting human BBB selectivity. This model provides a physiologically relevant platform for neurovascular research and drug screening.
Subject Keywords
blood–brain barrier
,
electrospun fibrous membrane
,
hydrogel-based brain microenvironment
,
in vitro model
,
neurovascular unit (NVU) model
,
tissue engineering
URI
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105021200064&origin=inward
https://hdl.handle.net/11511/117185
Journal
Journal of Biomedical Materials Research - Part A
DOI
https://doi.org/10.1002/jbm.a.38013
Collections
Graduate School of Natural and Applied Sciences, Article
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
G. E. Kole, Z. T. KOCAGÖZ, V. N. Hasırcı, and D. YÜCEL, “Establishment of an In Vitro Neurovascular Unit Model With Blood and Brain Components and Investigation of Its Blood–Brain Barrier,”
Journal of Biomedical Materials Research - Part A
, vol. 113, no. 11, pp. 0–0, 2025, Accessed: 00, 2025. [Online]. Available: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105021200064&origin=inward.