Notch4 and Jagged-1 Induce Microvessel Differentiation of Rat Brain Endothelial Cells

The mouse Notch4 gene is expressed specifically in endothelial cells. Notch4/int-3, a truncated form of Notch4, acts as a constitutive activated Notch receptor. We used rat brain microvessel endothelial cells (RBE4) to study the role of Notch4 and Jagged-1 in endothelial cell differentiation. Both N...

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Veröffentlicht in:Microvascular research 2000-09, Vol.60 (2), p.91-103
Hauptverfasser: Uyttendaele, Hendrik, Closson, Violaine, Wu, Guangyu, Roux, Françoise, Weinmaster, Gerry, Kitajewski, Jan
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Sprache:eng
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Zusammenfassung:The mouse Notch4 gene is expressed specifically in endothelial cells. Notch4/int-3, a truncated form of Notch4, acts as a constitutive activated Notch receptor. We used rat brain microvessel endothelial cells (RBE4) to study the role of Notch4 and Jagged-1 in endothelial cell differentiation. Both Notch4/int-3 and Jagged-1 were able to induce microvessel-like structures with morphological and biochemical properties similar to brain endothelial microvessels. Ectopic expression of full-length Notch4 did not effect RBE4 cells. Activation of the Notch signal transduction pathway was measured by the induction of endogenous Notch4 and Jagged-1 genes and of Jagged-1 proteins. The observed morphological changes to RBE4 cells correlated with endogenous Notch4 and Jagged-1 gene activation. Our observations demonstrate that Notch signaling can promote endothelial cell differentiation and morphogenesis.
ISSN:0026-2862
1095-9319
DOI:10.1006/mvre.2000.2254