Decreased diacylglycerol metabolism enhances ERK activation and augments CD8+ T cell functional responses. J Biol Chem 2011 Feb 18;286(7):5254-65
Date
12/09/2010Pubmed ID
21138839Pubmed Central ID
PMC3037638DOI
10.1074/jbc.M110.171884Scopus ID
2-s2.0-79953141058 (requires institutional sign-in at Scopus site) 54 CitationsAbstract
Modulation of T cell receptor signal transduction in CD8(+) T cells represents a novel strategy toward enhancing the immune response to tumor. Recently, levels of guanine exchange factors, RasGRP and SOS, within T cells have been shown to represent a key determinant in the regulation of the analog to the digital activation threshold of Ras. One important for regulating activation levels of RasGRP is diacylglycerol (DAG), and its levels are influenced by diacylglycerol kinase-ζ (DGKζ), which metabolizes DAG into phosphatidic acid, terminating DAG-mediated Ras signaling. We sought to determine whether DGKζ-deficient CD8(+) T cells demonstrated enhanced in vitro responses in a manner predicted by the current model of Ras activation and to evaluate whether targeting this threshold confers enhanced CD8(+) T cell responsiveness to tumor. We observed that DGKζ-deficient CD8(+) T cells conform to most predictions of the current model of how RasGRP levels influence Ras activation. But our results differ in that the EC(50) value of stimulation is not altered for any T cell receptor stimulus, a finding that suggests a further degree of complexity to how DGKζ deficiency affects signals important for Ras and ERK activation. Additionally, we found that DGKζ-deficient CD8(+) T cells demonstrate enhanced responsiveness in a subcutaneous lymphoma model, implicating the analog to a digital conversion threshold as a novel target for potential therapeutic manipulation.
Author List
Riese MJ, Grewal J, Das J, Zou T, Patil V, Chakraborty AK, Koretzky GAMESH terms used to index this publication - Major topics in bold
AnimalsCD8-Positive T-Lymphocytes
Diacylglycerol Kinase
Diglycerides
Enzyme Activation
Extracellular Signal-Regulated MAP Kinases
Lymphoma
Mice
Mice, Knockout
Models, Immunological
Neoplasms, Experimental
ras Proteins
