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Blood, 15 February 2004, Vol. 103, No. 4, pp. 1370-1372.
Prepublished online as a Blood First Edition Paper on October 23, 2003; DOI 10.1182/blood-2003-05-1701.


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HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY
Brief report

Dual roles of the C-terminal Src kinase (Csk) during developmental vascularization

Li-Juan Duan, Akira Imamoto, and Guo-Hua Fong

From the Center for Vascular Biology, University of Connecticut Health Center, Farmington; Department of Cell Biology, University of Connecticut Health Center, Farmington; Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington; The Ben May Institute for Cancer Research and Center for Molecular Oncology, University of Chicago, Chicago, IL.

Here we report that C-terminal Src kinase (Csk), a tyrosine kinase that negatively regulates the activity of Src and related kinases, is important for vascular development. In Csk/ embryos, although vascular tubules were formed and organized into capillary-like networks during the initial genesis of blood vessels, the vessels failed to engage in normal sprout formation. In chimeric embryos containing both wild-type and Csk/ cells, the presence of wild-type cells enabled Csk/ endothelial cells to participate in branching morphogenesis. We suggest that wild-type cells may have supplied an angiogenic factor absent in Csk/ cells. Despite the partial rescue of vascular development in chimeric embryos, the embryos failed to form vitelline vessels and died at E9.5. These results indicate that Csk is required both for angiogenic sprouting and vascular remodeling.


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L. Labrecque, C. Nyalendo, S. Langlois, Y. Durocher, C. Roghi, G. Murphy, D. Gingras, and R. Beliveau
Src-mediated Tyrosine Phosphorylation of Caveolin-1 Induces Its Association with Membrane Type 1 Matrix Metalloproteinase
J. Biol. Chem., December 10, 2004; 279(50): 52132 - 52140.
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