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Requirement of vasculogenesis and blood circulation in late stages of liver growth in zebrafish
Authors:Svetlana Korzh  Xiufang Pan  Marta Garcia-Lecea  Cecilia Lanny Winata  Xiaotao Pan  Thorsten Wohland  Vladimir Korzh  Zhiyuan Gong
Institution:1. Centro Interdisciplinar de Investiga??o em Sanidade Animal, Faculdade de Medicina Veterinária, Technical University of Lisbon, Lisboa, Portugal
2. Instituto Gulbenkian de Ciência, Oeiras, Portugal
7. Max Planck Institute for Molecular Biomedicine, Muenster, Germany
3. Sakaguchi Laboratory of Developmental Biology, School of Medicine, Keio University, Tokyo, Japan
4. Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisboa, Portugal
5. Department of Pathology, University of Southern California Keck School of Medicine, Los Angeles, CA, USA
6. Program for Developmental Biology, Hospital for Sick Children, Toronto, Canada
Abstract:

Background

In the vascular system, Notch receptors and ligands are expressed mainly on arteries, with Delta-like 4 (Dll4) being the only ligand known to be expressed early during the development of arterial endothelial cells and capillaries. Dll4 null embryos die very early in development with severely reduced arterial calibre and lumen and loss of arterial cell identity.

Results

The current detailed analysis of these mutants shows that the arterial defect precedes the initiation of blood flow and that the arterial Dll4 -/- endothelial cells proliferate and migrate more actively. Dll4 -/- mutants reveal a defective basement membrane around the forming aorta and increased endothelial cell migration from the dorsal aorta to peripheral regions, which constitute the main causes of arterial lumen reduction in these embryos. The increased proliferation and migration of Dll4 -/- endothelial cells was found to coincide with increased expression of the receptors VEGFR-2 and Robo4 and with downregulation of the TGF-β accessory receptor Endoglin.

Conclusion

Together, these results strongly suggest that Notch signalling can increase arterial stability and calibre by decreasing the response of arterial endothelial cells to local gradients of pro-angiogenic factors like VEGF.
Keywords:
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