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Publication : Differential regulation of primary and memory CD8 T cell immune responses by diacylglycerol kinases.

First Author  Shin J Year  2012
Journal  J Immunol Volume  188
Issue  5 Pages  2111-7
PubMed ID  22271650 Mgi Jnum  J:181278
Mgi Id  MGI:5310688 Doi  10.4049/jimmunol.1102265
Citation  Shin J, et al. (2012) Differential regulation of primary and memory CD8 T cell immune responses by diacylglycerol kinases. J Immunol 188(5):2111-7
abstractText  The manipulation of signals downstream of the TCR can have profound consequences for T cell development, function, and homeostasis. Diacylglycerol (DAG) produced after TCR stimulation functions as a secondary messenger and mediates the signaling to Ras-MEK-Erk and NF-kappaB pathways in T cells. DAG kinases (DGKs) convert DAG into phosphatidic acid, resulting in termination of DAG signaling. In this study, we demonstrate that DAG metabolism by DGKs can serve a crucial function in viral clearance upon lymphocytic choriomeningitis virus infection. Ag-specific CD8(+) T cells from DGKalpha(-/-) and DGKzeta(-/-) mice show enhanced expansion and increased cytokine production after lymphocytic choriomeningitis virus infection, yet DGK-deficient memory CD8(+) T cells exhibit impaired expansion after rechallenge. Thus, DGK activity plays opposing roles in the expansion of CD8(+) T cells during the primary and memory phases of the immune response, whereas consistently inhibiting antiviral cytokine production.
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