Expression and trafficking of MR1
Open accessAbstract
Summary: MHC class I‐related gene protein (MR1) is a non‐polymorphic MHC class IB antigen‐presenting molecule that is the restricting molecule for mucosal‐associated invariant T (MAIT) cells, a prominent population of innate‐like antibacterial T cells. The MAIT cell–MR1 axis represents a new paradigm in antigen presentation, with the MR1 ligand derived from vitamin B compounds or their metabolic precursors. Many bacteria and some fungi produce the activating ligand for MR1. In evolution, MR1 is highly conserved in most, but not all, mammals. In humans and rodents it is expressed in a broad range of cell types, both haematopoietic and non‐haematopoietic, although cell surface expression has been difficult to detect. Although MR1 trafficking shares features with both the MHC class I and MHC class II pathways, it is distinct. Several strands of evidence suggest that the intracellular location where MR1 is loaded differs for soluble ligand and for ligand derived from intact bacteria. The regulation of MR1 surface expression may also vary between different cell types. This paper will review what is currently known about the expression and trafficking of MR1 and propose a model for the loading and trafficking of MR1.
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MR1 mostly traffics intracellularly within LAMP1+ late endosomes/lysosomes.
“Although MR1 mostly traffics intracellularly within LAMP1+ late endosomes/lysosomes, 32 , 33”
From The MR1/MAIT cell axis enhances dystrophic neurite development in Alzheimer's disease (2025) · cites this paper as [33]
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Li, Y., Huang, B., Jiang, X., Chen, W., Zhang, J., Wei, Y., Chen, Y., Lian, M., Bian, Z., Miao, Q., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01994 · Cited by 107 · see citing works
The MR1/MAIT cell axis enhances dystrophic neurite development in Alzheimer's disease
Wyatt‐Johnson, S. K., Ackley, S., Warren, J., Priya, R., Wan, J., Liu, S., & Brutkiewicz, R. R. (2025) · Alzheimer's & Dementia · doi:10.1002/alz.14480 · Cited by 4 · see citing works
- Authors
- Lamichhane, R., & Ussher, J. E.
- Affiliations
- University of Otago (NZ)
- Corresponding author
- Ussher, James E.
- Venue
- Immunology
- Publisher
- Wiley
- Published
- 2017-05-18
- Volume
- 151
- Issue
- 3
- Pages
- 270-279
- ISSN
- 0019-2805 (ISSN-L)
- 1365-2567
- PMC
- PMC5461101
- OpenAlex
- W2606512914
- Cited by
- 45
- References
- 0
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 7 · 2023: 1 · 2022: 6 · 2021: 6 · 2020: 4 · 2019: 7 · 2018: 3 · 2017: 4
- FWCI
- 0.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Immunology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Keywords
- MR1, mucosal-associated invariant T cells, antigen presentation, antigen loading, MHC class Ib, innate-like T cells, bacterial ligands
- MeSH terms
- Amino Acid Sequence, Animals, Gene Expression Regulation, Humans, Ligands, RNA, Messenger, T-Lymphocytes, Histocompatibility Antigens Class I, Signal Transduction, Minor Histocompatibility Antigens, Conserved Sequence, Evolution, Molecular, Protein Transport
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