Biosynthesis of Sulfated L-Selectin Ligands in Human High Endothelial Venules (HEV)

  • Jean-Philippe Girard
  • François Amalric
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 435)


High endothelial venules (HEVs) are specialized post-capillary venules found in lymphoid tissues, that support high levels of lymphocyte extravasation from the blood. Lymphocyte L-selectin plays a key role in the initial interaction of lymphocytes with HEVs by recognizing sulfated carbohydrate ligands on HEV mucin-like glycoproteins, GlyCAM-1, CD34 and MAdCAM-1. Sulfation is key to the uniqueness of the HEV ligands since 6 or 6′sulfated-sLex isoforms have recently been identified as major capping groups of GlyCAM-1 and sulfation of both GlyCAM1 and CD34 has been shown to be required for high-affinity L-selectin binding and recognition by the HEV-specific monoclonal antibody MECA-79. To characterize the molecular mechanisms involved in the biosynthesis of sulfated L-selectin ligands in HEVs, we have started to isolate genes that play a role in sulfate metabolism in HEVs. Studies with chlorate, a selective inhibitor of the synthesis of the high energy donor of sulfate, PAPS (3′-phosphoadénosine 5′-phosphosulfate), had previously revealed that PAPS synthesis is required for sulfation of HEV ligands and recognition by L-selectin. Therefore, we screened an HEV cDNA library in order to isolate cDNAs encoding enzymes involved in PAPS synthesis. This strategy allowed us to isolate a novel cDNA encoding the PAPS synthetase from human HEVs. The molecular characteristics of PAPS synthetase and its role in biosynthesis of sulfated L-selectin ligands in HEVs are discussed.


Sulfate Transporter High Endothelial Venule Lymphocyte Migration Lymphocyte Homing Sulfate Incorporation 
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Copyright information

© Springer Science+Business Media New York 1998

Authors and Affiliations

  • Jean-Philippe Girard
    • 1
  • François Amalric
    • 1
  1. 1.Laboratoire de Biologie Moléculaire Eucaryote du CNRSToulouseFrance

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