Diverse MR1-restricted T cells in mice and humans.
Hui-Fern KoayNicholas A GherardinCalvin XuRebecca SeneviratnaZhe ZhaoZhenjun ChenDavid P FairlieJames McCluskeyDaniel G PellicciAdam P UldrichDale I GodfreyPublished in: Nature communications (2019)
Mucosal-associated invariant T (MAIT) cells express an invariant TRAV1/TRAJ33 TCR-α chain and are restricted to the MHC-I-like molecule, MR1. Whether MAIT cell development depends on this invariant TCR-α chain is unclear. Here we generate Traj33-deficient mice and show that they are highly depleted of MAIT cells; however, a residual population remains and can respond to exogenous antigen in vitro or pulmonary Legionella challenge in vivo. These residual cells include some that express Trav1+ TCRs with conservative Traj-gene substitutions, and others that express Trav1- TCRs with a broad range of Traj genes. We further report that human TRAV1-2- MR1-restricted T cells contain both MAIT-like and non-MAIT-like cells, as judged by their TCR repertoire, antigen reactivity and phenotypic features. These include a MAIT-like population that expresses a public, canonical TRAV36+ TRBV28+ TCR. Our findings highlight the TCR diversity and the resulting potential impact on antigen recognition by MR1-restricted T cells.
Keyphrases
- induced apoptosis
- regulatory t cells
- cell cycle arrest
- magnetic resonance
- contrast enhanced
- healthcare
- endothelial cells
- endoplasmic reticulum stress
- genome wide
- mental health
- emergency department
- oxidative stress
- stem cells
- cell death
- single cell
- metabolic syndrome
- computed tomography
- pulmonary hypertension
- adipose tissue
- dendritic cells
- signaling pathway
- cell therapy
- skeletal muscle
- mesenchymal stem cells
- bone marrow
- transcription factor
- electronic health record
- adverse drug