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Sphingosine-1-phosphate receptor 2 restrains egress of ?? T cells from the skin.


ABSTRACT: Maintenance of a population of IL-17-committed ?? T cells in the dermis is important in promoting tissue immunity. However, the signals facilitating ?? T cell retention within the dermis remain poorly understood. Here, we find that sphingosine-1-phosphate receptor 2 (S1PR2) acts in a cell-intrinsic manner to oppose ?? T cell migration from the dermis to the skin draining lymph node (dLN). Migration of dermal ?? T cells to the dLN under steady-state conditions occurs in an S1PR1-dependent manner. S1PR1 and CD69 are reciprocally expressed on dermal ?? T cells, with loss of CD69 associated with increased S1PR1 expression and enhanced migration to the dLN. ?? T cells lacking both S1PR2 and CD69 are impaired in their maintenance within the dermis. These findings provide a mechanism for how IL-17+ ?? T cells establish residence within the dermis and identify a role for S1PR2 in restraining the egress of tissue-resident lymphocytes.

SUBMITTER: Laidlaw BJ 

PROVIDER: S-EPMC6605748 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

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Sphingosine-1-phosphate receptor 2 restrains egress of γδ T cells from the skin.

Laidlaw Brian J BJ   Gray Elizabeth E EE   Zhang Yang Y   Ramírez-Valle Francisco F   Cyster Jason G JG  

The Journal of experimental medicine 20190603 7


Maintenance of a population of IL-17-committed γδ T cells in the dermis is important in promoting tissue immunity. However, the signals facilitating γδ T cell retention within the dermis remain poorly understood. Here, we find that sphingosine-1-phosphate receptor 2 (S1PR2) acts in a cell-intrinsic manner to oppose γδ T cell migration from the dermis to the skin draining lymph node (dLN). Migration of dermal γδ T cells to the dLN under steady-state conditions occurs in an S1PR1-dependent manner.  ...[more]

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