Back to Search
Start Over
Disruption of the Extracellular Matrix Progressively Impairs Central Nervous System Vascular Maturation Downstream of β-Catenin Signaling
- Source :
- Arteriosclerosis, thrombosis, and vascular biology, 39 (7, Arteriosclerosis, Thrombosis, and Vascular Biology
- Publication Year :
- 2019
-
Abstract
- Objective- The Wnt/β-catenin pathway orchestrates development of the blood-brain barrier, but the downstream mechanisms involved at different developmental windows and in different central nervous system (CNS) tissues have remained elusive. Approach and Results- Here, we create a new mouse model allowing spatiotemporal investigations of Wnt/β-catenin signaling by induced overexpression of Axin1, an inhibitor of β-catenin signaling, specifically in endothelial cells ( Axin1 iEC- OE). AOE (Axin1 overexpression) in Axin1 iEC- OE mice at stages following the initial vascular invasion of the CNS did not impair angiogenesis but led to premature vascular regression followed by progressive dilation and inhibition of vascular maturation resulting in forebrain-specific hemorrhage 4 days post-AOE. Analysis of the temporal Wnt/β-catenin driven CNS vascular development in zebrafish also suggested that Axin1 iEC- OE led to CNS vascular regression and impaired maturation but not inhibition of ongoing angiogenesis within the CNS. Transcriptomic profiling of isolated, β-catenin signaling-deficient endothelial cells during early blood-brain barrier-development (E11.5) revealed ECM (extracellular matrix) proteins as one of the most severely deregulated clusters. Among the 20 genes constituting the forebrain endothelial cell-specific response signature, 8 ( Adamtsl2, Apod, Ctsw, Htra3, Pglyrp1, Spock2, Ttyh2, and Wfdc1) encoded bona fide ECM proteins. This specific β-catenin-responsive ECM signature was also repressed in Axin1 iEC- OE and endothelial cell-specific β-catenin-knockout mice ( Ctnnb1-KOiEC) during initial blood-brain barrier maturation (E14.5), consistent with an important role of Wnt/β-catenin signaling in orchestrating the development of the forebrain vascular ECM. Conclusions- These results suggest a novel mechanism of establishing a CNS endothelium-specific ECM signature downstream of Wnt-β-catenin that impact spatiotemporally on blood-brain barrier differentiation during forebrain vessel development. Visual Overview- An online visual overview is available for this article.<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published
- Subjects :
- 0301 basic medicine
Male
vasculature
Angiogenesis
Cell- och molekylärbiologi
extracellular matrix
Vascular Remodeling
Blood–brain barrier
Vascular Regression
Extracellular matrix
03 medical and health sciences
Mice
0302 clinical medicine
Prosencephalon
Axin Protein
AXIN1
medicine
Animals
Zebrafish
Wnt Signaling Pathway
beta Catenin
biology
Basic Sciences
Wnt signaling pathway
Sciences bio-médicales et agricoles
blood-brain barrier
biology.organism_classification
central nervous system
basement membrane
endothelial cells
Cell biology
Mice, Inbred C57BL
030104 developmental biology
medicine.anatomical_structure
embryonic development
Forebrain
ComputingMethodologies_DOCUMENTANDTEXTPROCESSING
Cardiology and Cardiovascular Medicine
030217 neurology & neurosurgery
Cell and Molecular Biology
Signal Transduction
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Arteriosclerosis, thrombosis, and vascular biology, 39 (7, Arteriosclerosis, Thrombosis, and Vascular Biology
- Accession number :
- edsair.doi.dedup.....06033b6ff3ba417f3df4c5de13c061af