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MGL-mediated internalization and antigen presentation by dendritic cells: a role for tyrosine-5

  • Sandra J. van Vliet
  • , Corlien A. Aarnoudse
  • , Venice C. M. Broks-van den Berg
  • , Martine Boks
  • , Teunis B. H. Geijtenbeek
  • , Yvette van Kooyk

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Professional antigen-presenting cells are essential for the initiation of adaptive immune responses; however, they also play a vital role in the maintenance of tolerance towards self-antigens. C-type lectins can function as antigen receptors by capturing carbohydrate ligands for processing and presentation. Here, we focused on the dendritic cell (DC)-expressed macrophage galactose-type lectin (MGL), a C-type lectin with a unique specificity for terminal GalNAc residues, such as the tumor-associated Tn antigen. Soluble model antigens are efficiently internalized by MGL and subsequently presented to responder CD4+ T cells. The tyrosine-5 residue in the YENF motif, present in the MGL cytoplasmic domain, was essential for the MGL-mediated endocytosis in CHO cells. In conclusion, MGL contributes to the antigen processing and presentation capacities of DC and may provide a suitable target for the initiation of anti-tumor immune responses
Original languageEnglish
Pages (from-to)2075-2081
JournalEuropean journal of immunology
Volume37
Issue number8
DOIs
Publication statusPublished - 2007

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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