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The FGF system has a key role in regulating vascular integrity
Masahiro Murakami, Loc T. Nguyen, Zhen W. Zhang, Karen L. Moodie, Peter Carmeliet, Radu V. Stan, Michael Simons
Masahiro Murakami, Loc T. Nguyen, Zhen W. Zhang, Karen L. Moodie, Peter Carmeliet, Radu V. Stan, Michael Simons
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Research Article Vascular biology

The FGF system has a key role in regulating vascular integrity

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Abstract

The integrity of the endothelial monolayer is essential to blood vessel homeostasis and active regulation of endothelial permeability. The FGF system plays important roles in a wide variety of physiologic and pathologic conditions; however, its role in the adult vasculature has not been defined. To assess the role of the FGF system in the adult endothelial monolayer, we disrupted FGF signaling in bovine aortic endothelial cells and human saphenous vein endothelial cells in vitro and in adult mouse and rat endothelial cells in vivo using soluble FGF traps or a dominant inhibitor of all FGF receptors. The inhibition of FGF signaling using these approaches resulted in dissociation of the VE-cadherin/p120-catenin complex and disassembly of adherens and tight junctions, which progressed to loss of endothelial cells, severe impairment of the endothelial barrier function, and finally, disintegration of the vasculature. Thus, FGF signaling plays a key role in the maintenance of vascular integrity.

Authors

Masahiro Murakami, Loc T. Nguyen, Zhen W. Zhang, Karen L. Moodie, Peter Carmeliet, Radu V. Stan, Michael Simons

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Figure 3

In vivo effect of FGF inhibition in the endothelium.

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In vivo effect of FGF inhibition in the endothelium.
(A) Enface preparat...
(A) Enface preparation of the rat femoral artery transduced with Ad-Null or Ad-FGFR1DN (109 PFUs). Segments of arteries were transduced with adenoviruses and stained for VE-cadherin (red) and maximum intensity projection of 1-μm Z-Stack sections is shown. At day 5, endothelial cells lost cell-cell contacts and gaps formed between cells. Scale bars: 10 μm. (B) Mouse carotid artery and jugular vein exposed to systemic Ad-Null or Ad-sFGFR1IIIc viruses. Segments of arteries were stained for VE-cadherin, and maximum intensity projection of 1-μm Z-Stack sections is shown. Scale bars: 20 μm.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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