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B Cell Induction of IL-13 Expression in NK Cells: Role of CD244 and SLAM-Associated Protein
Author(s) -
Ning Gao,
Pamela Schwartzberg,
Julie A. Wilder,
Bruce R. Blazar,
Dorothy Yuan
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.5.2758
Subject(s) - microbiology and biotechnology , janus kinase 3 , interleukin 21 , interleukin 12 , biology , secretion , cd49b , nk 92 , cell , immune system , immunology , cytotoxic t cell , t cell , in vitro , biochemistry , genetics
NK cells are an important component of the innate immune system that can also interact with B cells in a mutually productive manner. We have previously shown that activated B cells can induce NK cells to up-regulate their secretion of IFN-gamma. In this study, we show that B cells, and, particularly, marginal zone B cells, can, in addition, induce NK cells via direct cell-cell interactions to express mRNA encoding the Th2 cytokine IL-13. The induction of NK cell IL-13 mRNA expression requires the ligation of the CD244 receptor by the CD48 ligand on B cells via signaling pathways that depend upon expression of the X-linked lymphoproliferative disease gene product, SH2D1A/DSHP/SAP (SLAM-associated protein, or SAP) in NK cells. Thus, the positive signals attributed to the B cell activation of CD244 on murine NK cells appears to be more similar to the activity of CD244 on human cells. The induction of IL-13 mRNA by B cells may account for the effect of NK cells on the generation of Th2-type responses in the presence of some adjuvants.

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