Department of Microbiology and Immunology, University of Melbourne, Peter Doherty Institute for Infection and Immunity, Victoria, Australia.
Infection and Immunity Program, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Nat Immunol. 2016 May;17(5):531-7. doi: 10.1038/ni.3416. Epub 2016 Apr 4.
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.
递呈分子 MR1 通过一种尚未明确的途径将维生素 B 相关抗原(VitB 抗原)递呈给黏膜相关不变 T(MAIT)细胞。我们发现,MR1 与其他抗原递呈分子不同,它不会组成性地递呈自身配体。在稳态下,它在内质网中以配体接受构象积累。VitB 抗原到达该位置并与 MR1 形成 Schiff 碱,触发“分子开关”,使 MR1-VitB 抗原复合物能够转运到质膜。这些复合物以与 MR1-配体相互作用亲和力无关的动力学被内吞,并在细胞内降解,尽管一些 MR1 分子在通过内体时获得新的配体并循环回表面。MR1 抗原递呈的特点是快速的“开-关-开”机制,该机制严格依赖于抗原的可用性。