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Memory formation and long-term maintenance of IL-7R?+ ILC1s via a lymph node-liver axis.


ABSTRACT: Natural killer (NK) cells are reported to have immunological memory, with CD49a+ liver-resident NK cells shown to confer hapten-specific memory responses, but how this memory is induced or maintained is unclear. Here we show that memory type I innate lymphoid cells (ILC1s), which express IL-7R?, are generated in the lymph nodes (LNs) and require IL-7R signaling to maintain their longevity in the liver. Hapten sensitization initiates CXCR3-dependent recruitment of IL-7R?+ ILC1s into skin-draining LNs, where they are primed and acquire hapten-specific memory potential. Memory IL-7R?+ ILC1s then exit draining LNs and are preferentially recruited, via CXCR6, to reside in the liver. Moreover, long-term blockade of IL-7R signaling significantly reduces ILC1-mediated memory responses. Thus, our results identify a memory IL-7R?+ ILC1 population and reveal a LN-liver axis that is essential for ILC1 memory generation and long-term maintenance.

SUBMITTER: Wang X 

PROVIDER: S-EPMC6242895 | biostudies-other | 2018 Nov

REPOSITORIES: biostudies-other

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Memory formation and long-term maintenance of IL-7Rα<sup>+</sup> ILC1s via a lymph node-liver axis.

Wang Xianwei X   Peng Hui H   Cong Jingjing J   Wang Xuefu X   Lian Zhexiong Z   Wei Haiming H   Sun Rui R   Tian Zhigang Z  

Nature communications 20181119 1


Natural killer (NK) cells are reported to have immunological memory, with CD49a<sup>+</sup> liver-resident NK cells shown to confer hapten-specific memory responses, but how this memory is induced or maintained is unclear. Here we show that memory type I innate lymphoid cells (ILC1s), which express IL-7Rα, are generated in the lymph nodes (LNs) and require IL-7R signaling to maintain their longevity in the liver. Hapten sensitization initiates CXCR3-dependent recruitment of IL-7Rα<sup>+</sup> IL  ...[more]

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