The Journal of Experimental Medicine
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Published online November 17, 2008
doi:10.1084/jem.20080406
The Journal of Experimental Medicine, Vol. 205, No. 12, 2929-2945
The Rockefeller University Press, 0022-1007 $30.00
© 2008 Nottebaum et al.
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ARTICLE

VE-PTP maintains the endothelial barrier via plakoglobin and becomes dissociated from VE-cadherin by leukocytes and by VEGF

Astrid F. Nottebaum1, Giuseppe Cagna1, Mark Winderlich1, Alexander C. Gamp1, Ruth Linnepe1, Christian Polaschegg1, Kristina Filippova1, Ruth Lyck2, Britta Engelhardt2, Olena Kamenyeva1, Maria Gabriele Bixel1, Stefan Butz1, and Dietmar Vestweber1

1 Max-Planck-Institute of Molecular Biomedicine, 48149 Münster, Germany
2 Theodor Kocher Institute, University of Bern, 3012 Bern, Switzerland

CORRESPONDENCE Dietmar Vestweber: vestweb{at}mpi-muenster.mpg.de

We have shown recently that vascular endothelial protein tyrosine phosphatase (VE-PTP), an endothelial-specific membrane protein, associates with vascular endothelial (VE)–cadherin and enhances VE-cadherin function in transfected cells (Nawroth, R., G. Poell, A. Ranft, U. Samulowitz, G. Fachinger, M. Golding, D.T. Shima, U. Deutsch, and D. Vestweber. 2002. EMBO J. 21:4885–4895). We show that VE-PTP is indeed required for endothelial cell contact integrity, because down-regulation of its expression enhanced endothelial cell permeability, augmented leukocyte transmigration, and inhibited VE-cadherin–mediated adhesion. Binding of neutrophils as well as lymphocytes to endothelial cells triggered rapid (5 min) dissociation of VE-PTP from VE-cadherin. This dissociation was only seen with tumor necrosis factor {alpha}–activated, but not resting, endothelial cells. Besides leukocytes, vascular endothelial growth factor also rapidly dissociated VE-PTP from VE-cadherin, indicative of a more general role of VE-PTP in the regulation of endothelial cell contacts. Dissociation of VE-PTP and VE-cadherin in endothelial cells was accompanied by tyrosine phoshorylation of VE-cadherin, β-catenin, and plakoglobin. Surprisingly, only plakoglobin but not β-catenin was necessary for VE-PTP to support VE-cadherin adhesion in endothelial cells. In addition, inhibiting the expression of VE-PTP preferentially increased tyrosine phosphorylation of plakoglobin but not β-catenin. In conclusion, leukocytes interacting with endothelial cells rapidly dissociate VE-PTP from VE-cadherin, weakening endothelial cell contacts via a mechanism that requires plakoglobin but not β-catenin.


Abbreviations used: CHO, Chinese hamster ovary; ESAM, endothelial cell–selective adhesion molecule; GST, glutathione S-transferase; HUVEC, human umbilical vein endothelial cell; ICAM, intercellular adhesion molecule; JAM, junctional adhesion molecule; PECAM-1, platelet endothelial cell adhesion molecule; siRNA, small interfering RNA; VE, vascular endothelial; VEGF, vascular endothelial growth factor; VE-PTP, vascular endothelial protein tyrosine phosphatase.

© 2008 Nottebaum et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).


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