Mannosylated glycans impair normal T-cell development by reprogramming commitment and repertoire diversity
Manuel M. Vicente, Inês Alves, Ângela Fernandes, Ana M. Dias, Beatriz Santos‐Pereira, Elena Pérez-Anton, Sofia Santos, Tao Yang, Alexandra Correia, Anja Münster-Kühnel, Afonso R. M. Almeida, Sarina Ravens, Gabriel A. Rabinovich, Manuel Vilanova, Ana E. Sousa, Salomé S. Pinho
Abstract
Abstract T-cell development ensures the formation of diverse repertoires of T-cell receptors (TCRs) that recognize a variety of antigens. Glycosylation is a major posttranslational modification present in virtually all cells, including T-lymphocytes, that regulates activity/functions. Although these structures are known to be involved in TCR-selection in DP thymocytes, it is unclear how glycans regulate other thymic development processes and how they influence susceptibility to disease. Here, we discovered stage-specific glycome compositions during T-cell development in human and murine thymocytes, as well as dynamic alterations. After restricting the N -glycosylation profile of thymocytes to high-mannose structures, using specific glycoengineered mice ( Rag1 Cre Mgat1 fl/fl ), we showed remarkable defects in key developmental checkpoints, including ß-selection, regulatory T-cell generation and γδT-cell development, associated with increased susceptibility to colon and kidney inflammation and infection. We further demonstrated that a single N -glycan antenna (modeled in Rag1 Cre Mgat2 fl/fl mice) is the sine-qua-non condition to ensure normal development. In conclusion, we revealed that mannosylated thymocytes lead to a dysregulation in T-cell development that is associated with inflammation susceptibility.