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Development and trafficking of type 1 and type 17 mucosal-associated invariant T cells

Descrizione del progetto

Sviluppo di cellule T invarianti associate alla mucosa

Le cellule T invarianti associate alla mucosa (MAIT) sono un sottogruppo unico di cellule T che svolgono un ruolo cruciale nella difesa immunitaria, in particolare nei siti mucosali come l’intestino, i polmoni e altri tessuti barriera. Esprimono un recettore di cellule T semi-invariante che riconosce i metaboliti di origine microbica. Il progetto MAIT-TraDe, finanziato dal programma di azioni Marie Skłodowska-Curie, vuole capire come le cellule MAIT si sviluppano e migrano dal timo ai tessuti della mucosa. I ricercatori studieranno il ruolo dei metaboliti microbici nell’adattamento e nel mantenimento delle cellule MAIT nei tessuti. Nel complesso, i risultati del progetto sveleranno i meccanismi cruciali che regolano la biologia e la funzione omeostatica delle cellule MAIT.

Obiettivo

Mucosal-associated invariant T (MAIT) cells colonize mucosal tissues where they become tissue-resident and have important protective and homeostatic functions. MAIT cells are selected in the thymus by microbial metabolites presented by MHC-related protein 1 (MR1) on thymocytes thereby acquiring an effector phenotype (type 1 or 17). This project aims at elucidating mechanisms that regulate the last stages of thymic MAIT cell development, including their egress, and identify cues necessary for tissue colonization. Specifically, we will couple transcriptomics and thymus transplantation models to analyze canonical thymic MAIT cell development, thereby identifying new regulators of the MAIT1/17 fates, as well as to identify MAIT cells that recently exited the thymus and seeded mucosal organs, thereby identifying new regulators of tissue adaptation. These targets will be functionally tested in models combining CRISPR/Cas9 encoded by lentivirus with bone-marrow chimeras or adoptive transfers. Additionally, we will determine the identity and dynamics of MAIT cells exiting the thymus to colonize tissues by combining different experimental approaches including in vivo EdU/biotin labeling, thymectomy and blockage of thymus egress. Lastly, we will address whether MR1–microbial metabolites are required for the maintenance of MAIT cells in tissues at steady-state using mono-colonization/decolonization of germ-free mice and by conditionally ablating Mr1. Overall, this work will uncover fundamental mechanisms underlying MAIT cell development and tissue colonization. Albeit outside the scope of this work, it is possible that the mechanisms uncovered here may have implications in other innate-like T cells or for the establishment of mainstream tissue-resident T cells.

Coordinatore

INSTITUT CURIE
Contribution nette de l'UE
€ 195 914,88
Indirizzo
RUE D ULM 26
75231 Paris
Francia

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Regione
Ile-de-France Ile-de-France Paris
Tipo di attività
Research Organisations
Collegamenti
Costo totale
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