A conserved transcriptional program for MAIT cells across mammalian evolution

哺乳动物进化过程中MAIT细胞的保守转录程序

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作者:Hélène Bugaut # ,Yara El Morr # ,Martin Mestdagh ,Aurélie Darbois ,Rafael A Paiva ,Marion Salou ,Laetitia Perrin ,Mariela Fürstenheim ,Anastasia du Halgouet ,Linda Bilonda-Mutala ,Anne-Laure Le Gac ,Manon Arnaud ,Ahmed El Marjou ,Coralie Guerin ,Atitheb Chaiyasitdhi ,Julie Piquet ,David M Smadja ,Agata Cieslak ,Bernhard Ryffel ,Valdone Maciulyte ,James M A Turner ,Karine Bernardeau ,Xavier Montagutelli ,Olivier Lantz # ,François Legoux #

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.

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