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Lopez-Ramirez, Miguel Alejandro; Male, David Kingsley; Wang, Chunfang; Sharrack, Basil; Wu, Dongsheng and Romero, Ignacio Andres
(2013).
DOI: https://doi.org/10.1186/2045-8118-10-27
Abstract
Background: The human cerebral microvascular endothelial cell line, hCMEC/D3, has been used extensively to
model the blood–brain barrier (BBB) in vitro. Recently, we reported that cytokine-treatment induced loss of brain
endothelial barrier properties. In this study, we further determined the gene expression pattern of hCMEC/D3 cells
in response to activation with TNFα and IFNγ.
Findings: Using a microarray approach, we observed that expression of genes involved in the control of barrier
permeability, including inter-brain endothelial junctions (e.g. claudin-5, MARVELD-2), integrin-focal adhesions
complexes (e.g. integrin β1, ELMO-1) and transporter systems (e.g. ABCB1, SLC2A1), are altered by pro-inflammatory
cytokines.
Conclusions: Our study shows that previously-described cytokine-induced changes in the pattern of gene expression of endothelium are reproduced in hCMEC/D3 cells, suggesting that this model is suitable to study inflammation at the BBB, while at the same time it has provided insights into novel key molecular processes that are altered in brain endothelium during neuroinflammation, such as modulation of cell-to-matrix contacts.