L-selectin ligands that are O-glycoprotease resistant and distinct from MECA-79 antigen are sufficient for tethering and rolling of lymphocytes on human high endothelial venules

During the process of lymphocyte recirculation, lymphocytes bind via L-selectin to sulfated sialyl-Lewis(x) (sLe(x))-containing carbohydrate ligands expressed on the surface of high endothelial venules (HEV). We have examined the expression of sLe(x) on HEV using a panel of mAbs specific for sLe(x) and sLe(x)-related structures, and have examined the function of different sLe(x)-bearing structures using an in vitro assay of lymphocyte rolling on HEV, We report that three sLe(x) mAbs, 2F3, 2H5, and CSLEX-1, previously noted to bind with high affinity to glycolipid-linked sLe(x), vary in their ability to stain HEV in different lymphoid tis sues and bind differentially to O-linked versus N-linked sLe(x) on glycoproteins, Treatment of tissue sections with neuraminidase abolished staining with all three mAbs but slightly increased staining with MECA-79, a mAb to a sulfation-dependent HEV-associated carbohydrate determinant. Treatment of tissue sections with O-sialoglycoprotease under conditions that removed the vast majority of MECA-79 staining, only partially reduced staining with the 2F3 and 2H5 mAbs. Using a novel rolling assay in which cells bind under flow to HEV of frozen tissue sections, we demonstrate that a pool of O-sialoglycoprotease-resistant molecules is present on HEV that is sufficient for attachment and rolling of lymphocytes via L-selectin, This interaction is not inhibited by the mAb MECA-79, Furthermore, MECA-79 mAb blocks binding to untreated sections by only 30%, whereas the sLe(x) mAb 2H5 blocks binding by similar to 60% and a combination of MECA-79 and 2H5 mAb blocks binding by 75%. We conclude that a pool of O-glycoprotease-resistant sLe(x)-like L-selectin ligands exist on human HEV that is distinct from the mucin-associated moieties recognized by MECA-79 mAb. We postulate that these ligands may participate in lymphocyte binding to HEV.