Article
- The EMBO Journal (2003) 22, 3772 - 3782
- doi:10.1093/emboj/cdg382
Subject Category:
The guanylate binding protein-1 GTPase controls the invasive and angiogenic capability of endothelial cells through inhibition of MMP-1 expression
Eric Guenzi1, Kristin Töpolt1, Clara Lubeseder-Martellato1, Anita Jörg1, Elisabeth Naschberger1, Roberto Benelli2, Adriana Albini2 and Michael Stürzl1,3
- Department of Virus-induced Vasculopathy, Institute of Molecular Virology, GSF-National Research Center for Environment and Health, Neuherberg, D-85764, Germany
- Centro di Biotecnologie Avanzate, Istituto Nazionale per la Ricerca sul Cancro, 16132 Genova, Italy
- Department of Surgery, Section of Molecular and Experimental Surgery, University of Erlangen-Nürnberg, D-91054 Erlangen, Germany
Correspondence to:
Michael Stürzl, E-mail: Michael.stuerzl@chir.imed.uni-erlangen.de
Received 17 December 2002; Accepted 11 June 2003; Revised 20 May 2003
Abstract
Expression of the large GTPase guanylate binding protein-1 (GBP-1) is induced by inflammatory cytokines (ICs) in endothelial cells (ECs), and the helical domain of the molecule mediates the repression of EC proliferation by ICs. Here we show that the expression of GBP-1 and of the matrix metalloproteinase-1 (MMP-1) are inversely related in vitro and in vivo, and that GBP-1 selectively inhibits the expression of MMP-1 in ECs, but not the expression of other proteases. The GTPase activity of GBP-1 was necessary for this effect, which inhibited invasiveness and tube-forming capability of ECs in three-dimensional collagen-I matrices. A GTPase-deficient mutant (D184N-GBP-1) operated as a transdominant inhibitor of wild-type GBP-1 and rescued MMP-1 expression in the presence of ICs. Expression of D184N-GBP-1, as well as paracrine supplementation of MMP-1, restored the tube-forming capability of ECs in the presence of wild-type GBP-1. The latter finding indicated that the inhibition of capillary formation is specifically due to the repression of MMP-1 expression by GBP-1, and is not affected by the anti-proliferative activity of the helical domain of GBP-1. These findings substantiate the role of GBP-1 as a major regulator of the anti-angiogenic response of ECs to ICs.
Keywords:
- angiogenesis,
- collagenase,
- inflammation,
- invasion,
- MMP



