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Diversity in medullary thymic epithelial cells controls the activity and availability of iNKT cells.


ABSTRACT: The thymus supports multiple ?? T cell lineages that are functionally distinct, but mechanisms that control this multifaceted development are poorly understood. Here we examine medullary thymic epithelial cell (mTEC) heterogeneity and its influence on CD1d-restricted iNKT cells. We find three distinct mTEClow subsets distinguished by surface, intracellular and secreted molecules, and identify LT?R as a cell-autonomous controller of their development. Importantly, this mTEC heterogeneity enables the thymus to differentially control iNKT sublineages possessing distinct effector properties. mTEC expression of LT?R is essential for the development thymic tuft cells which regulate NKT2 via IL-25, while LT?R controls CD104+CCL21+ mTEClow that are capable of IL-15-transpresentation for regulating NKT1 and NKT17. Finally, mTECs regulate both iNKT-mediated activation of thymic dendritic cells, and iNKT availability in extrathymic sites. In conclusion, mTEC specialization controls intrathymic iNKT cell development and function, and determines iNKT pool size in peripheral tissues.

SUBMITTER: Lucas B 

PROVIDER: S-EPMC7198500 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Diversity in medullary thymic epithelial cells controls the activity and availability of iNKT cells.

Lucas Beth B   White Andrea J AJ   Cosway Emilie J EJ   Parnell Sonia M SM   James Kieran D KD   Jones Nick D ND   Ohigashi Izumi I   Takahama Yousuke Y   Jenkinson William E WE   Anderson Graham G  

Nature communications 20200504 1


The thymus supports multiple αβ T cell lineages that are functionally distinct, but mechanisms that control this multifaceted development are poorly understood. Here we examine medullary thymic epithelial cell (mTEC) heterogeneity and its influence on CD1d-restricted iNKT cells. We find three distinct mTEC<sup>low</sup> subsets distinguished by surface, intracellular and secreted molecules, and identify LTβR as a cell-autonomous controller of their development. Importantly, this mTEC heterogenei  ...[more]

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