Angiopoietin-2, a Natural Antagonist for Tie2 That Disrupts in vivo Angiogenesis

Author:

Maisonpierre Peter C.1,Suri Chitra1,Jones Pamela F.1,Bartunkova Sona1,Wiegand Stanley J.1,Radziejewski Czeslaw1,Compton Debra1,McClain Joyce1,Aldrich Thomas H.1,Papadopoulos Nick1,Daly Thomas J.1,Davis Samuel1,Sato Thomas N.1,Yancopoulos George D.1

Affiliation:

1. P. C. Maisonpierre, C. Suri, P. F. Jones, S. J. Wiegand, C. Radziejewski, D. Compton, J. McClain, T. H. Aldrich, N. Papadopoulos, T. J. Daly, S. Davis, and G. D. Yancopoulos are at Regeneron Pharmaceuticals Inc., 777 Old Saw Mill River Road, Tarrytown, NY 10591, USA. S. Bartunkova and T. N. Sato are at Beth Israel–Deaconess Medical Center and Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.

Abstract

Angiogenesis is thought to depend on a precise balance of positive and negative regulation. Angiopoietin-1 (Ang1) is an angiogenic factor that signals through the endothelial cell–specific Tie2 receptor tyrosine kinase. Like vascular endothelial growth factor, Ang1 is essential for normal vascular development in the mouse. An Ang1 relative, termed angiopoietin-2 (Ang2), was identified by homology screening and shown to be a naturally occurring antagonist for Ang1 and Tie2. Transgenic overexpression of Ang2 disrupts blood vessel formation in the mouse embryo. In adult mice and humans, Ang2 is expressed only at sites of vascular remodeling. Natural antagonists for vertebrate receptor tyrosine kinases are atypical; thus, the discovery of a negative regulator acting on Tie2 emphasizes the need for exquisite regulation of this angiogenic receptor system.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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