A conserved transcriptional program for MAIT cells across mammalian evolution.
Hélène BugautYara El MorrMartin MestdaghAurelie Darbois-DelahousseRafael A PaivaMarion SalouLaetitia PerrinMariela FürstenheimAnastasia du HalgouetLinda Bilonda MutalaAnne-Laure Le GacManon ArnaudAhmed El MarjouCoralie L GuerinAtitheb ChaiyasitdhiJulie PiquetDavid M SmadjaAgata CieslakBernhard RyffelValdone MaciulyteJames M A TurnerKarine BernardeauXavier MontagutelliOlivier LantzFrancois LegouxPublished in: The Journal of experimental medicine (2023)
Mucosal-associated invariant T (MAIT) cells harbor evolutionarily conserved TCRs, suggesting important functions. As human and mouse MAIT functional programs appear distinct, the evolutionarily conserved MAIT functional features remain unidentified. Using species-specific tetramers coupled to single-cell RNA sequencing, we characterized MAIT cell development in six species spanning 110 million years of evolution. Cross-species analyses revealed conserved transcriptional events underlying MAIT cell maturation, marked by ZBTB16 induction in all species. MAIT cells in human, sheep, cattle, and opossum acquired a shared type-1/17 transcriptional program, reflecting ancestral features. This program was also acquired by human iNKT cells, indicating common differentiation for innate-like T cells. Distinct type-1 and type-17 MAIT subsets developed in rodents, including pet mice and genetically diverse mouse strains. However, MAIT cells further matured in mouse intestines to acquire a remarkably conserved program characterized by concomitant expression of type-1, type-17, cytotoxicity, and tissue-repair genes. Altogether, the study provides a unifying view of the transcriptional features of innate-like T cells across evolution.
Keyphrases
- single cell
- induced apoptosis
- cell cycle arrest
- transcription factor
- endothelial cells
- immune response
- gene expression
- quality improvement
- escherichia coli
- cell death
- signaling pathway
- adipose tissue
- genome wide
- oxidative stress
- skeletal muscle
- cell therapy
- computed tomography
- insulin resistance
- pet ct
- heat shock protein
- pet imaging