Back to Search Start Over

A conserved transcriptional program for MAIT cells across mammalian evolution.

Authors :
Bugaut H
El Morr Y
Mestdagh M
Darbois A
Paiva RA
Salou M
Perrin L
Fürstenheim M
du Halgouet A
Bilonda-Mutala L
Le Gac AL
Arnaud M
El Marjou A
Guerin C
Chaiyasitdhi A
Piquet J
Smadja DM
Cieslak A
Ryffel B
Maciulyte V
Turner JMA
Bernardeau K
Montagutelli X
Lantz O
Legoux F
Source :
The Journal of experimental medicine [J Exp Med] 2024 Feb 05; Vol. 221 (2). Date of Electronic Publication: 2023 Dec 20.
Publication Year :
2024

Abstract

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.<br /> (© 2023 Bugaut et al.)

Details

Language :
English
ISSN :
1540-9538
Volume :
221
Issue :
2
Database :
MEDLINE
Journal :
The Journal of experimental medicine
Publication Type :
Academic Journal
Accession number :
38117256
Full Text :
https://doi.org/10.1084/jem.20231487