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Am J Physiol Heart Circ Physiol 291: H2126-H2135, 2006. First published May 5, 2006; doi:10.1152/ajpheart.00185.2006
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Growth factor- and heparin-dependent regulation of constitutive and agonist-mediated human endothelial barrier function

Alan B. Moy,1,2 Ken Blackwell,5 Mack H. Wu,4 and Harris J. Granger3

1Cellular Engineering Technologies, Inc., 2Departments of Biomedical Engineering and 5Pathology, University of Iowa, Iowa City, Iowa; 3Department of Medical Physiology, Texas A & M University Health Science Center, Temple, Texas; and 4Department of Surgery, University of California Davis Medical Center, Sacramento, California

Submitted 21 February 2006 ; accepted in final form 27 April 2006

We report functional differences in constitutive and agonist-mediated endothelial barrier function between cultured primary and Clonetics human umbilical vein endothelial cells (pHUVEC and cHUVEC) grown in soluble growth factors and heparin. Basal transendothelial resistance (TER) was much lower in pHUVEC than in cHUVEC grown in medium supplemented with growth factors, such as basic fibroblast growth factor (bFGF), vascular endothelial growth factor (VEGF), and human epithelial growth factor (EGF), and heparin. On the basis of a numerical model of TER, the increased basal TER in cHUVEC was due to effects on cell-matrix adhesion and membrane capacitance. Heparin and bFGF increased constitutive TER in cultured pHUVEC, and heparin mediated additional increases in constitutive TER in pHUVEC supplemented with bFGF. EGF attenuated bFGF-mediated increases in TER. On the basis of the numerical model, in contrast to cHUVEC, heparin and bFGF augmented TER through effects on cell-cell adhesion and membrane capacitance in pHUVEC. Thrombin mediated quantitatively greater amplitude and a more sustained decline in TER in cultured cHUVEC than pHUVEC. Thrombin-mediated barrier dysfunction was attenuated in pHUVEC conditioned in EGF in the presence or absence of heparin. Thrombin-mediated barrier dysfunction was also attenuated when monolayers were exposed to low concentrations of heparin and further attenuated in the presence of bFGF. cAMP stimulation mediated differential attenuation of thrombin-mediated barrier dysfunction between pHUVEC and cHUVEC. VEGF displayed differential effects in TER in serum-free medium. Taken together, these data demonstrate marked differential regulation of constitutive and agonist-mediated endothelial barrier function in response to mitogens and heparin stimulation.

commercial endothelial; fibroblast growth factor; vascular endothelial growth factor; epithelial growth factor; numerical modeling of transendothelial resistance



Address for reprint requests and other correspondence: A. B. Moy, Cellular Engineering Technologies, Inc., 2501 Crosspark Rd., Ste. B105, Coralville, IA 52241 (e-mail: moya{at}celleng-tech.com)







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