Analysis of the Phenotype and Function of the Subpopulations of Mucosal-Associated Invariant T Cells
Language English Country Great Britain, England Media print
Document type Journal Article
PubMed
27474379
DOI
10.1111/sji.12467
Knihovny.cz E-resources
- MeSH
- Biomarkers metabolism MeSH
- Cell Lineage immunology MeSH
- CD8-Positive T-Lymphocytes cytology immunology MeSH
- Adult MeSH
- Gene Expression MeSH
- GPI-Linked Proteins genetics immunology MeSH
- Granzymes genetics immunology MeSH
- Immunophenotyping MeSH
- Immunologic Memory * MeSH
- Interferon-gamma genetics immunology MeSH
- NK Cell Lectin-Like Receptor Subfamily K genetics immunology MeSH
- Middle Aged MeSH
- Humans MeSH
- Mucosal-Associated Invariant T Cells cytology immunology MeSH
- Lysosomal-Associated Membrane Protein 1 genetics immunology MeSH
- Receptors, IgG genetics immunology MeSH
- Tumor Necrosis Factor-alpha genetics immunology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- FCGR3B protein, human MeSH Browser
- GPI-Linked Proteins MeSH
- Granzymes MeSH
- GZMB protein, human MeSH Browser
- IFNG protein, human MeSH Browser
- Interferon-gamma MeSH
- KLRK1 protein, human MeSH Browser
- NK Cell Lectin-Like Receptor Subfamily K MeSH
- Lysosomal-Associated Membrane Protein 1 MeSH
- Receptors, IgG MeSH
- Tumor Necrosis Factor-alpha MeSH
Mucosal-associated invariant T (MAIT) cells contain two main subpopulations, CD8(+) and double-negative (DN) cells. The first reports suggested that subpopulations of MAIT cells have similar phenotype and function. Recent works, however, demonstrate that the subpopulations have different ontogenesis and are differentially affected by xenobiotic treatment. In this work, we re-examined the possible differences between subpopulations of MAIT cells. We demonstrate that the main subpopulations of MAIT cells (CD8 and DN) are relatively uniform in terms of both phenotype and function. Both populations are memory/activated, tissue-homing and pro-inflammatory. CD8(+) MAIT cells are better equipped for pro-inflammatory functions as they express higher levels of CD16 and NKG2D, produce more pro-inflammatory cytokines (TNF-α and IFN-γ) and have higher cytotoxic potential (contain more granzyme B and express higher levels of CD107A upon stimulation). Our study contributes to the understanding of the heterogeneity of MAIT cell population.
References provided by Crossref.org
Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)