@article{lymph 3672, author = {X Wu, N-F Liu}, title = {THE ROLE OF ANG/TIE SIGNALING IN LYMPHANGIOGENESIS}, volume = {43}, year = {2010}, url = {http://journals.librarypublishing.arizona.edu/lymph/article/id/3672/}, issue = {2}, abstract = {<p>The angiopoietin/Tie system plays a key role in remodeling and maturation of blood vessels as well as lymphatic vessels. The angiopoietin family includes four ligands (Ang-1,Ang-2 and Ang-3/4) and two corresponding tyrosine kinase receptors (Tie1 and Tie2). The best characterized angiopoietins are Ang-1and Ang-2. Ang-1 acts as an obligate agonist of the Tie2 receptor. Binding of Ang-1 to Tie2induces its autophosphorylation and promotes vascular stability and integrity. Ang-1 induces lymphatic vessel enlargement, sprouting and proliferation in a VEGFR-3-dependentmanner. In contrast, whether Ang-2 is agonistic or antagonistic is dependent on dose and context. Ang-2 modulates angiogenesis in a cooperative manner with another important angiogenic factor, vascular endothelial growth factor A. In the presence of VEGF-A, Ang-2promotes vascular sprouting. When in the absence of VEGF-A, Ang-2 induces vascular regression. However, genetic studies have revealed that Ang-2-deficient mice exhibit more severe defects in the lymphatic vasculature than in blood vessels. Ang-2 seems to be involved in the remodeling and stabilization of lymphatic vessels. Although the Ang/Tie system is essential for blood and lymphatic vessel remodeling and maturation, defining its precise role in blood and lymphatic development has been a major challenge. This review provides an update on our current understanding of the angiopoietin/Tie system inlymphangiogenesis.</p>}, month = {8}, pages = {59-72}, keywords = {lymphatic,Ang/Tie2 signaling,lymphangiogenesis}, issn = {2522-7963}, publisher={International Society of Lymphology and the University of Arizona Libraries}, journal = {Lymphology} }