| Literature DB >> 25903786 |
Cornelia Podjaski1, Jorge I Alvarez2, Lyne Bourbonniere2, Sandra Larouche2, Simone Terouz2, Jenea M Bin3, Marc-André Lécuyer2, Olivia Saint-Laurent2, Catherine Larochelle2, Peter J Darlington3, Nathalie Arbour2, Jack P Antel3, Timothy E Kennedy3, Alexandre Prat4.
Abstract
Blood-brain barrier function is driven by the influence of astrocyte-secreted factors. During neuroinflammatory responses the blood-brain barrier is compromised resulting in central nervous system damage and exacerbated pathology. Here, we identified endothelial netrin 1 induction as a vascular response to astrocyte-derived sonic hedgehog that promotes autocrine barrier properties during homeostasis and increases with inflammation. Netrin 1 supports blood-brain barrier integrity by upregulating endothelial junctional protein expression, while netrin 1 knockout mice display disorganized tight junction protein expression and barrier breakdown. Upon inflammatory conditions, blood-brain barrier endothelial cells significantly upregulated netrin 1 levels in vitro and in situ, which prevented junctional breach and endothelial cell activation. Finally, netrin 1 treatment during experimental autoimmune encephalomyelitis significantly reduced blood-brain barrier disruption and decreased clinical and pathological indices of disease severity. Our results demonstrate that netrin 1 is an important regulator of blood-brain barrier maintenance that protects the central nervous system against inflammatory conditions such as multiple sclerosis and experimental autoimmune encephalomyelitis.Entities:
Keywords: blood–brain barrier; experimental autoimmune encephalomyelitis; multiple sclerosis; netrin 1; neuroinflammation
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Year: 2015 PMID: 25903786 PMCID: PMC4614143 DOI: 10.1093/brain/awv092
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501