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Sci. STKE, 13 November 2007
Vol. 2007, Issue 412, p. re8
[DOI: 10.1126/stke.4122007re8]

REVIEWS

Dual Regulation of Endothelial Junctional Permeability

Yulia A. Komarova{dagger}, Dolly Mehta{dagger}, and Asrar B. Malik*

Department of Pharmacology and Center for Lung and Vascular Biology, University of Illinois College of Medicine, Chicago, IL 60612, USA.
{dagger}These authors contributed equally to this work.

Abstract: G protein–coupled receptors (GPCRs) of endothelial cells transmit diverse intracellular signals that regulate adherens junction (AJ) permeability. Increased endothelial permeability contributes to pathological processes such as inflammation, atherogenesis, and acute lung injury. Thrombin, a serine protease, and sphingosine-1-phosphate (S1P), a bioactive lipid, regulate endothelial barrier function by activating their respective GPCRs—the protease-activated receptor PAR1 and the S1P receptor S1P1—which initiate intracellular signals that regulate AJ integrity and cytoskeleton organization. The distinct patterns of PAR1 and S1P1 signal transduction underlie the functional antagonism between thrombin and S1P. Evidence points to a role for activation of the S1P1 receptor that is induced by PAR1-mediated signaling in the mechanism of AJ reannealing and endothelial barrier repair. Understanding the molecular basis of AJ integrity in the context of inflammation is important in developing novel anti-inflammatory therapeutics. This Review provides a working model for molecular mechanisms for the dual regulation of endothelial barrier function.

*Corresponding author. E-mail, abmalik{at}uic.edu

Citation: Y. A. Komarova, D. Mehta, A. B. Malik, Dual Regulation of Endothelial Junctional Permeability. Sci. STKE 2007, re8 (2007).

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