Lectin binding to gp60 decreases specific albumin binding and transport in pulmonary artery endothelial monolayers

Publisher Website
Google Scholar
Abstract
The effect of albumin binding to cultured bovine pulmonary artery endothelial cell (BPAEC) monolayers on the transendothelial flux of 125I‐labelled bovine serum albumin (BSA) was examined to determine its possible role on albumin transcy‐tosis. The transport of 125I‐BSA tracer across BPAEC grown on gelatin‐ and fibronectin‐coated filters (0.8 μm pore diam.) was affected by the presence of unlabelled BSA in the medium in that transendothelial 125I‐BSA permeability decreased, reaching a 40% reduction at BSA concentrations equal to or greater than 5 mg/ml. BSA binding to BPAEC monolayers was saturated at concentration of 10 mg/ml with an apparent binding affinity of 6 x 10−7 M. In contrast, gelatin added to the medium altered neither 125I‐BSA binding nor transport. Several lectins were tested for their ability to inhibit 125I‐BSA binding and transport. One lectin, Ricinus communis (RCA), reduced 125I‐BSA binding by 70% and transport by 40%. Other lectins, Ulex europaeus, Triticum vulgare, and Glycine max decreased neither 125I‐BSA binding nor transport. The reduction of 125I‐BSA transport by RCA was not observed in the presence of saturating levels of BSA, indicating that RCA influenced only the albumin‐dependent component of transport. RCA, but not other lectins, precipitated a 60 kDa plasmalemmal glycoprotein from cell lysates of surface radioiodinated BPAEC monolayers. This 60 kDa glycoprotein appears to be the equivalent of gp60 identified previously as an albumin binding glycoprotein in rat microvascular endothelium. In summary, approximately 40% of albumin transport across' BPAEC monolayers is dependent on albumin binding. This component of albumin transport is inhibited by 80% by the binding of RCA to gp60. These results suggest that binding of albumin to gp60 on pulmonary artery endothelial cell membrane is a critical determinant of transendothelial albumin flux involving mechanisms such as plasmalemmal vesicular transcytosis.