The NFκB-inducing kinase is essential for the developmental programming of skin-resident and IL-17-producing γδ T cells

  1. Florian Mair
  2. Stefanie Joller
  3. Romy Hoeppli
  4. Lucas Onder
  5. Matthias Hahn
  6. Burkhard Ludewig
  7. Ari Waisman
  8. Burkhard Becher  Is a corresponding author
  1. University of Zurich, Switzerland
  2. University of British Columbia, Canada
  3. Kantonsspital St. Gallen, Switzerland
  4. Johannes Gutenberg University of Mainz, Germany

Abstract

γδ T cells contribute to first line immune defense, particularly through their ability for rapid production of proinflammatory cytokines. The cytokine profile of γδ T cells is hard-wired already during thymic development. Yet, the molecular pathways underlying this phenomenon are incompletely understood. Here we show that signaling via the NFκB inducing kinase (NIK) is essential for the formation of a fully functional γδ T cell compartment. In the absence of NIK, development of Vγ5+ dendritic epidermal T cells (DETCs) was halted in the embryonic thymus, and impaired NIK function caused a selective loss of IL-17 expression by γδ T cells. Using a novel conditional mutant of NIK, we could show in vivo that NIK signaling in thymic epithelial cells is essential for the thymic hardwiring of γδ T cell cytokine production.

Article and author information

Author details

  1. Florian Mair

    Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland
    Competing interests
    The authors declare that no competing interests exist.
  2. Stefanie Joller

    Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland
    Competing interests
    The authors declare that no competing interests exist.
  3. Romy Hoeppli

    Department of Surgery / Child and Family Research Institute, University of British Columbia, Vancouver, Canada
    Competing interests
    The authors declare that no competing interests exist.
  4. Lucas Onder

    Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland
    Competing interests
    The authors declare that no competing interests exist.
  5. Matthias Hahn

    Institute for Molecular Medicine, Johannes Gutenberg University of Mainz, Mainz, Germany
    Competing interests
    The authors declare that no competing interests exist.
  6. Burkhard Ludewig

    Institute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland
    Competing interests
    The authors declare that no competing interests exist.
  7. Ari Waisman

    Institute for Molecular Medicine, Johannes Gutenberg University of Mainz, Mainz, Germany
    Competing interests
    The authors declare that no competing interests exist.
  8. Burkhard Becher

    Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland
    For correspondence
    becher@immunology.uzh.ch
    Competing interests
    The authors declare that no competing interests exist.

Reviewing Editor

  1. Fiona M Powrie, University of Oxford, United Kingdom

Ethics

Animal experimentation: All animal experiments were approved by local authorities (Swiss cantonal veterinary office Zurich, KVET license numbers 86/2012, 70/2015, 100/2015 and 68/2013) and performed in strict accordance with the corresponding license.

Version history

  1. Received: July 15, 2015
  2. Accepted: December 2, 2015
  3. Accepted Manuscript published: December 5, 2015 (version 1)
  4. Version of Record published: January 14, 2016 (version 2)

Copyright

© 2015, Mair et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

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  1. Florian Mair
  2. Stefanie Joller
  3. Romy Hoeppli
  4. Lucas Onder
  5. Matthias Hahn
  6. Burkhard Ludewig
  7. Ari Waisman
  8. Burkhard Becher
(2015)
The NFκB-inducing kinase is essential for the developmental programming of skin-resident and IL-17-producing γδ T cells
eLife 4:e10087.
https://doi.org/10.7554/eLife.10087

Share this article

https://doi.org/10.7554/eLife.10087

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