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This Article Full Text Full Text (PDF) All Versions of this Article: 286/2/H731    most recent 00427.2003v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (15) Citing Articles via Google Scholar Google Scholar Articles by DeMaio, L. Articles by Antonetti, D. A. Search for Related Content PubMed PubMed Citation Articles by DeMaio, L. Articles by Antonetti, D. A.

A transmural pressure gradient induces mechanical and biological adaptive responses in endothelial cells

¹Department of Chemical Engineering, Biomolecular Transport Dynamics Laboratory, The Pennsylvania State University, University Park 16802; Departments of ²Cellular and Molecular Physiology and ³Ophthalmology, Penn State College of Medicine, Hershey, Pennsylvania 17033; and ⁴Department of Biomedical Engineering, The City College of The City University of New York, New York, New York 10031

Submitted 2 May 2003 ; accepted in final form 27 September 2003

A sudden increase in the transmural pressure gradient across endothelial monolayers reduces hydraulic conductivity (L_p), a phenomenon known as the sealing effect. To further characterize this endothelial adaptive response, we measured bovine aortic endothelial cell (BAEC) permeability to albumin and 70-kDa dextran, L_p, and the solvent-drag reflection coefficients () during the sealing process. The diffusional permeability coefficients for albumin (1.33 ± 0.18 x 10^–6 cm/s) and dextran (0.60 ± 0.16 x 10^–6 cm/s) were measured before pressure application. The effective permeabilities (measured when solvent drag contributes to solute transport) of albumin and dextran (P_ealb and P_edex) were measured after the application of a 10 cmH₂O pressure gradient; during the first 2 h of pressure application, P_ealb, P_edex, and L_p were significantly reduced by 2.0 ± 0.3-, 2.1 ± 0.3-, and 3.7 ± 0.3-fold, respectively. Immunostaining of the tight junction (TJ) protein zonula occludens-1 (ZO-1) was significantly increased at cell-cell contacts after the application of transmural pressure. Cytochalasin D treatment significantly elevated transport but did not inhibit the adaptive response, whereas colchicine treatment had no effect on diffusive permeability but inhibited the adaptive response. Neither cytoskeletal inhibitor altered despite significantly elevating both L_p and effective permeability. Our data suggest that BAECs actively adapt to elevated transmural pressure by mobilizing ZO-1 to intercellular junctions via microtubules. A mechanical (passive) component of the sealing effect appears to reduce the size of a small pore system that allows the transport of water but not dextran or albumin. Furthermore, the structures of the TJ determine transport rates but do not define the selectivity of the monolayer to solutes ().

permeability; hydraulic conductivity; reflection coefficient; zonula occludens-1

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