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A Critical Role of Costimulation during Intrathymic Development of Invariant NK T Cells
Author(s) -
Yeonseok Chung,
Roza Nurieva,
Eiji Esashi,
Yi-Hong Wang,
Dapeng Zhou,
Laurent Gapin,
Chen Dong
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.4.2276
Subject(s) - cd80 , cd86 , microbiology and biotechnology , cd1d , foxp3 , biology , t cell , natural killer t cell , immunology , regulatory t cell , il 2 receptor , immune system , cd40 , cytotoxic t cell , in vitro , biochemistry
CD1d-restricted Valpha14(+) invariant NK T (iNKT) cells are a specialized alphabeta T cell subset that regulates both innate and adaptive immunity. Although costimulatory molecules are required for the activation of conventional T cells and for the development of Foxp3(+) T cells, their role in iNKT cell regulation is unclear. Here we report that mice deficient in CD80/CD86 and/or B7h exhibit severe defects in thymic iNKT cell maturation, associated with largely reduced iNKT cell number in the thymus and the periphery. We show that costimulation is necessary for the optimal expansion of postselected NK1.1(-) immature iNKT cells in the thymus and for the proper expression of the maturation markers T-bet and CD122. Surprisingly, costimulatory molecules on both hemopoietic and nonhematopoietic cells are required for iNKT cell development. Our results thus demonstrate a previously unknown function of costimulation in the intrathymic development of iNKT cells, distinct from that of conventional T cells and regulatory T cells.

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