| Literature DB >> 27043408 |
Hamish E G McWilliam1,2,3,4, Sidonia B G Eckle1, Alex Theodossis2, Ligong Liu5,6, Zhenjun Chen1, Jacinta M Wubben2,3,4, David P Fairlie5,6, Richard A Strugnell1, Justine D Mintern7, James McCluskey1, Jamie Rossjohn2,3,4,8, Jose A Villadangos1,7.
Abstract
The antigen-presenting molecule MR1 presents vitamin B-related antigens (VitB antigens) to mucosal-associated invariant T (MAIT) cells through an uncharacterized pathway. We show that MR1, unlike other antigen-presenting molecules, does not constitutively present self-ligands. In the steady state it accumulates in a ligand-receptive conformation within the endoplasmic reticulum. VitB antigens reach this location and form a Schiff base with MR1, triggering a 'molecular switch' that allows MR1-VitB antigen complexes to traffic to the plasma membrane. These complexes are endocytosed with kinetics independent of the affinity of the MR1-ligand interaction and are degraded intracellularly, although some MR1 molecules acquire new ligands during passage through endosomes and recycle back to the surface. MR1 antigen presentation is characterized by a rapid 'off-on-off' mechanism that is strictly dependent on antigen availability.Entities:
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Year: 2016 PMID: 27043408 DOI: 10.1038/ni.3416
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606