Brain astrocytes and microglia express functional MR1 molecules that present microbial antigens to mucosal-associated invariant T (MAIT) cells
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It is unknown whether brain astrocytes and microglia have the capacity to present microbial antigens via the innate immune MR1/MAIT cell axis. We have detected MAIT cells in the normal mouse brain and found that both astrocytes and microglia are MR1+. When we stimulated brain astrocytes and microglia with E. coli, and then co-cultured them with MAIT cells, MR1 surface expression was upregulated and MAIT cells were activated in an antigen-dependent manner. Considering the association of MAIT cells with inflammatory conditions, including those in the CNS, the MR1/MAIT cell axis could be a novel therapeutic target in neuroinflammatory disorders.
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Functional MR1 is expressed in the brain.
“we have recently shown that functional MR1 is expressed in the brain [14].”
From Control of the temporal development of Alzheimer’s disease pathology by the MR1/MAIT cell axis (2023) · cites this paper as [14]
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Sweeney, M. D., Zhao, Z., Montagne, A., Nelson, A. R., & Zlokovic, B. V. (2019) · Physiological Reviews · doi:10.1152/physrev.00050.2017 · Cited by 2,294 · see citing works
Neuroinflammation: The Devil Is in the Details
DiSabato, D. J., Quan, N., & Godbout, J. P. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13607 · Cited by 1,640 · see citing works
How do immune cells overcome the blood-brain barrier in multiple sclerosis?
Larochelle, C., Alvarez, J. I., & Prat, A. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.04.066 · Cited by 405 · see citing works
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Control of the temporal development of Alzheimer’s disease pathology by the MR1/MAIT cell axis
Wyatt-Johnson, S. K., Kersey, H. N., Codocedo, J. F., Newell, K. L., Landreth, G. E., Lamb, B. T., Oblak, A. L., & Brutkiewicz, R. R. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02761-6 · Cited by 22 · see citing works
“MAIT cells are the prototypic MR1-restricted T cell subpopulation [32, 33] and can easily be identified using MR1 tetramers [14, 34, 35].”
BackgroundMethodInfluentialSelf-citationThe 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
“In terms of NT-APP densitometry, there was a significant interaction between both the age of the mice and genotype ( F [1,11] = 19.55, P = 0.001).”
InfluentialSelf-citation
- Authors
- Priya, R., & Brutkiewicz, R. R.
- Affiliations
- Indiana University Indianapolis (US)
- Corresponding author
- Brutkiewicz, Randy R.
- Venue
- Journal of Neuroimmunology
- Publisher
- Elsevier BV
- Published
- 2020-12
- Volume
- 349
- Pages
- 577428
- ISSN
- 0165-5728 (ISSN-L)
- PMC
- PMC7680413
- OpenAlex
- W3093275938
- Cited by
- 18
- References
- 3
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 6 · 2023: 3 · 2022: 3 · 2021: 1
- FWCI
- 0.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Journal of Neuroimmunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- IUScholarWorks (Indiana University) (submittedVersion)
- Funders
- National Institutes of Health (R01 CA161178)
- Indiana Spinal Cord Injury and Brain Injury Grant Program
- Indiana University School of Medicine's Cooperative Center of Excellence in Hematology (U54 DK106846)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- MR1, mucosal-associated invariant T cells, astrocytes, microglia, antigen presentation, microbial antigens, brain, neuroinflammation, neuroinflammatory disorders, therapeutic target, co-culture, Escherichia coli
- MeSH terms
- Mucosal-Associated Invariant T Cells, Animals, Astrocytes, Brain, Cell Line, Female, Immunity, Innate, Male, Mice, Inbred C57BL, Histocompatibility Antigens Class I, Minor Histocompatibility Antigens, Microglia, Mice, Knockout, Mice
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