The Tec kinases Itk and Rlk regulate NKT cell maturation, cytokine production, and survival
The Tec kinases Itk and Rlk regulate NKT cell maturation, cytokine production, and survival
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DOI:
10.4049/jimmunol.180.5.3007
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发表时间:
2008-03-01
影响因子:
4.4
通讯作者:
Berg, Leslie J.
中科院分区:
文献类型:
--
作者:
Felices, Martin;Berg, Leslie J.
The Tec kinases Itk and Rlk are required for efficient positive selection of conventional CD4(+) and CD8(+) T cells in the thymus. In contrast, recent studies have shown that these Tec kinases are dispensable for the development of CD8(+) T cells with characteristics of innate T cells. These findings raise questions about the potential role of Itk and Rlk in NKT cell development, because NKT cells represent a subset of innate T cells. To address this issue, we examined invariant NKT cells in Itk(-/-) and Itk/Rlk(-/-) mice. We find, as has been reported previously, that Itk(-/-) mice have reduced numbers of NKT cells with a predominantly immature phenotype. We further show that this defect is greatly exacerbated in the absence of both Itk and Rlk, leading to a 7-fold reduction in invariant NKT cell numbers in the thymus of Itk/Rlk(-/-) mice and a more severe block in NKT cell maturation. Splenic Itk(-/-) and Itk/Rlk(-/-) NKT cells are also functionally defective, because they produce little to no cytokine following in vivo activation. Tec kinase-deficient NKT cells also show enhanced cell death in the spleen. These defects correlate with greatly diminished expression of CD122, the IL-2R/IL-15R beta-chain, and impaired expression of the T-box transcription factor, T-bet. These data indicate that the Tec kinases Itk and Rlk provide important signals for terminal maturation, efficient cytokine production, and peripheral survival of NKT cells.