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IL-4 and IL-4 Receptor Expression Is Dispensable for the Development and Function of Natural Killer T Cells
Author(s) -
Archna Sharma,
Rosa Berga-Bolaños,
Dil Afroz Sultana,
Jyoti Misra Sen
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0071872
Subject(s) - biology , natural killer t cell , microbiology and biotechnology , interleukin 12 , t cell receptor , interleukin 21 , cytokine , antigen , interleukin 15 , immunology , t cell , cytotoxic t cell , immune system , interleukin , in vitro , biochemistry
CD4 T cells acquire functional properties including cytokine production upon antigenic stimulation through the T cell receptor (TCR) and differentiate into T helper (Th) cells. Th1 cells produce interferon (IFN)-γ and Th2 cells produce interleukin (IL)-4. Th1 and 2 cells utilize IFN-γ and IL-4 for further maturation and maintenance, respectively. Promyelocytic leukemia zinc finger (PLZF)-expressing invariant natural killer T (iNKT) cells develop in the thymus and acquire functional ability to produce IL-4 and IFN-γ in the thymus in the absence of antigenic stimulation. In response to antigenic stimulation, iNKT cells rapidly produce IFN-γ and IL-4. However, it is still unknown as to whether iNKT cells require these cytokines for maturation or survival in vivo. In this study, using IL-4- and IL-4 receptor- (IL-4R) deficient mice, we demonstrate that IL-4 as well as IL-4R expression is dispensable for the development, function and maintenance of iNKT cells.

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