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Unraveling the influence of astrocytes on endothelial cell transcription : Towards understanding blood-brain barrier in vitro models’ dynamics

Zamproni, Laura Nicoleti ; Gökçe, Begüm ; Venckute Larsson, Justina ; Ceballos-Torres, Angela ; Gram, Magnus LU orcid ; Porcionatto, Marimélia Aparecida and Herland, Anna (2025) In Brain Research Bulletin 224.
Abstract

In recent years, considerable advancements have been made in developing in vitro models to better understand the complex dynamics of the blood-brain barrier (BBB) and its critical role in neurological health and disease. Incorporating astrocytes into these models introduces an essential layer of complexity, allowing for a more comprehensive investigation of the cellular interactions and regulatory mechanisms that maintain BBB integrity and functionality. Despite these advances, the specific influence of astrocytes on endothelial cells in in vitro systems remains inadequately explored. This study addresses this gap by examining the transcriptional changes in primary human brain microvascular endothelial cells (HBMECs) cocultured with... (More)

In recent years, considerable advancements have been made in developing in vitro models to better understand the complex dynamics of the blood-brain barrier (BBB) and its critical role in neurological health and disease. Incorporating astrocytes into these models introduces an essential layer of complexity, allowing for a more comprehensive investigation of the cellular interactions and regulatory mechanisms that maintain BBB integrity and functionality. Despite these advances, the specific influence of astrocytes on endothelial cells in in vitro systems remains inadequately explored. This study addresses this gap by examining the transcriptional changes in primary human brain microvascular endothelial cells (HBMECs) cocultured with human astrocytes (HAs). Our findings demonstrate that astrocytes profoundly modulate endothelial pathways involved in cell cycle regulation and division while upregulating genes associated with BBB integrity, protective mechanisms, and transporter activity. Furthermore, astrocytes significantly enhanced transendothelial electrical resistance (TEER) and reduced permeability to tracer Cascade Blue dye, confirming their functional impact on BBB models. By providing a comprehensive human primary cell dataset, this research underscores the pivotal role astrocytes play in shaping endothelial cell gene expression and function in contact coculture systems. These results emphasize the necessity of incorporating astrocytes into in vitro BBB models to accurately replicate neurovascular interactions. Ultimately, this study advances our understanding of BBB physiology and highlights the importance of refining in vitro models to better reflect the complexity of the human neurovascular environment, with potential implications for studying neurological disorders and drug delivery strategies.

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author
; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Blood-brain barrier, Human astrocytes, Human brain microvascular endothelial cells, Transcriptional changes
in
Brain Research Bulletin
volume
224
article number
111328
publisher
Elsevier
external identifiers
  • pmid:40174788
  • scopus:105001801984
ISSN
0361-9230
DOI
10.1016/j.brainresbull.2025.111328
language
English
LU publication?
yes
id
8aeaa8f8-d767-4b4f-9924-bcb3db3f8122
date added to LUP
2025-08-18 14:43:09
date last changed
2025-08-18 14:55:15
@article{8aeaa8f8-d767-4b4f-9924-bcb3db3f8122,
  abstract     = {{<p>In recent years, considerable advancements have been made in developing in vitro models to better understand the complex dynamics of the blood-brain barrier (BBB) and its critical role in neurological health and disease. Incorporating astrocytes into these models introduces an essential layer of complexity, allowing for a more comprehensive investigation of the cellular interactions and regulatory mechanisms that maintain BBB integrity and functionality. Despite these advances, the specific influence of astrocytes on endothelial cells in in vitro systems remains inadequately explored. This study addresses this gap by examining the transcriptional changes in primary human brain microvascular endothelial cells (HBMECs) cocultured with human astrocytes (HAs). Our findings demonstrate that astrocytes profoundly modulate endothelial pathways involved in cell cycle regulation and division while upregulating genes associated with BBB integrity, protective mechanisms, and transporter activity. Furthermore, astrocytes significantly enhanced transendothelial electrical resistance (TEER) and reduced permeability to tracer Cascade Blue dye, confirming their functional impact on BBB models. By providing a comprehensive human primary cell dataset, this research underscores the pivotal role astrocytes play in shaping endothelial cell gene expression and function in contact coculture systems. These results emphasize the necessity of incorporating astrocytes into in vitro BBB models to accurately replicate neurovascular interactions. Ultimately, this study advances our understanding of BBB physiology and highlights the importance of refining in vitro models to better reflect the complexity of the human neurovascular environment, with potential implications for studying neurological disorders and drug delivery strategies.</p>}},
  author       = {{Zamproni, Laura Nicoleti and Gökçe, Begüm and Venckute Larsson, Justina and Ceballos-Torres, Angela and Gram, Magnus and Porcionatto, Marimélia Aparecida and Herland, Anna}},
  issn         = {{0361-9230}},
  keywords     = {{Blood-brain barrier; Human astrocytes; Human brain microvascular endothelial cells; Transcriptional changes}},
  language     = {{eng}},
  publisher    = {{Elsevier}},
  series       = {{Brain Research Bulletin}},
  title        = {{Unraveling the influence of astrocytes on endothelial cell transcription : Towards understanding blood-brain barrier in vitro models’ dynamics}},
  url          = {{http://dx.doi.org/10.1016/j.brainresbull.2025.111328}},
  doi          = {{10.1016/j.brainresbull.2025.111328}},
  volume       = {{224}},
  year         = {{2025}},
}