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Am J Physiol Lung Cell Mol Physiol 289: L371-L381, 2005; doi:10.1152/ajplung.00175.2004
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Constitutive eNOS-derived nitric oxide is a determinant of endothelial junctional integrity

Dan Predescu, Sanda Predescu, Jun Shimizu, Kayo Miyawaki-Shimizu, and Asrar B. Malik

Department of Pharmacology, University of Illinois, College of Medicine, Chicago, Illinois

Submitted 17 May 2004 ; accepted in final form 24 March 2005

Basal vascular endothelial permeability is normally kept low in part by the restrictiveness of interendothelial junctions (IEJs). We investigated the possible role of nitric oxide (NO) in controlling IEJ integrity and thereby regulating basal vascular permeability. We determined the permeability of continuous endothelia in multiple murine vascular beds, including lung vasculature, of wild-type mice, endothelial nitric oxide synthase (eNOS) null mice, and mice treated with NOS inhibitor N-nitro-L-arginine methyl ester (L-NAME). Light and electron microscopic studies revealed that L-NAME treatment resulted in IEJs opening within a few minutes with a widespread response within 30 min. We observed a 35% increase in transendothelial transport of albumin, using as tracer dinitrophenylated albumin in mouse lungs and other organs studied. To rule out the involvement of blood cells in the mechanism of increased endothelial permeability, vascular beds were flushed free of blood, treated with L-NAME, and perfused with the tracer. The open IEJs observed in these studies indicated a direct role for NO in preserving the normal structure of endothelial junctions. We also used the electron-opaque tracer lanthanum chloride to assess vascular permeability. Lanthanum chloride was presented by perfusion to various vascular beds of mice lacking NO. Open IEJs were seen only in capillary and venular endothelial segments of mice lacking NO, and there was a concomitant increase in vascular permeability to the tracer. Together, these data demonstrate that constitutive eNOS-derived NO is a crucial determinant of IEJ integrity and thus serves to maintain the low basal permeability of continuous endothelia.

morphometric analysis; basal lung vascular permeability; interendothelial junctions; nitric oxide synthase inhibition; endothelial nitric oxide synthase knockout mice; transendothelial transport



Address for reprint requests and other correspondence: D. Predescu, Univ. of Illinois, College of Medicine, Dept. of Pharmacology, 835 S. Wolcott Ave., Chicago, IL 60612 (e-mail: Predescu{at}uic.edu)




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