Thrombin-induced endothelial barrier disruption in intact microvessels: role of RhoA/Rho kinase-myosin phosphatase axis

• Published in: American Journal of Physiology: Cell Physiology 2008-05, Vol.294 (5), p.C1234-C1241
• Main Authors: van Nieuw Amerongen, G. P, Musters, R. J. P, Eringa, E. C, Sipkema, P, van Hinsbergh, V. W. M
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Concanavalin A - pharmacology; Cytoskeleton; Endothelium, Vascular - drug effects; Endothelium, Vascular - physiology; Enzymes; Humans; Microcirculation - drug effects; Microcirculation - physiology; Myosin-Light-Chain Phosphatase - physiology; Proteins; Rats; Rats, Wistar; rho-Associated Kinases - physiology; rhoA GTP-Binding Protein - physiology; Three dimensional imaging; Thrombin - pharmacology; Umbilical Veins - drug effects; Umbilical Veins - physiology
• ISSN: 0363-6143; 1522-1563
• DOI: 10.1152/ajpcell.00551.2007

Laboratory for Physiology, Institute for Cardiovascular Research, Vrije Universiteit University Medical Center, Amsterdam, The Netherlands Submitted 20 November 2007 ; accepted in final form 5 March 2008 Endothelial hyperpermeability is regulated by a myosin light chain-2 (MLC2) phosphorylation-dependent contractile mechanism. Thrombin is a potent inducer of hyperpermeability of cultured monolayers of endothelial cells (ECs) via Rho kinase-mediated MLC2-phosphorylation. The aim of the present study was to investigate the effects of thrombin on in situ endothelial morphology and barrier integrity. Cytoskeletal dynamics, regions of paracellular flux, and MLC2-phosphorylation of ECs were visualized by digital three-dimensional imaging microscopy of pressurized rat kidney arterioles. Myosin phosphatase targeting subunit (MYPT1)-phosphorylation was used as a surrogate marker for Rho kinase activity. Thrombin induced the formation of F-actin filaments in ECs in situ and rounding of the ECs in the absence of obvious formation of gaps between ECs. These changes were accompanied by an increase in MLC2 phosphorylation and a decrease in barrier integrity. In vitro analysis revealed that Rho kinase activity on F-actin filaments was associated with a contractile response that enhanced opening of the barrier. Rho kinase activity was not detectable on F-actin filaments induced by histamine, an inducer of a more transient hyperpermeability response. Inhibition of the myosin phosphatase mimicked the effects of thrombin on barrier function. The thrombin-induced changes in in situ MLC2 phosphorylation and barrier function were Rho kinase dependent. These data demonstrate a direct effect of thrombin on EC morphology and barrier integrity in intact microvessels. Furthermore, they establish an important contribution of enhanced Rho kinase activity to the development of prolonged but not transient types of endothelial barrier dysfunction. vascular biology; three-dimensional digital imaging; cytoskeleton; stress fibers Address for reprint requests and other correspondence: G. P. van Nieuw Amerongen, VU Univ. Medical Center, Laboratory for Physiology, Boechorstraat 7, 1081BT, Amsterdam, The Netherlands (e-mail: nieuwamerongen{at}vumc.nl )