RasGRP is essential for mouse thymocyte differentiation and TCR signaling

The Ras signaling pathway plays a critical role in thymopoiesis and T cell activation, but the mechanism of Ras regulation is controversial. At least one mode of Ras regulation in T cells involves the messenger diacylglycerol (DAG). RasGRP, a Ras activator with a DAG-binding C1 domain, is expressed...

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Veröffentlicht in:Nature immunology 2000-10, Vol.1 (4), p.317-321
Hauptverfasser: Stone, James C, Dower, Nancy A, Stang, Stacey L, Bottorff, Drell A, Ebinu, Julius O, Dickie, Peter, Ostergaard, Hanne L
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Sprache:eng
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Zusammenfassung:The Ras signaling pathway plays a critical role in thymopoiesis and T cell activation, but the mechanism of Ras regulation is controversial. At least one mode of Ras regulation in T cells involves the messenger diacylglycerol (DAG). RasGRP, a Ras activator with a DAG-binding C1 domain, is expressed in T cells and thymocytes. Here we show that thymi of RasGRP-null mutant mice have approximately normal numbers of immature thymocytes but a marked deficiency of mature, single-positive (CD4+CD8- and CD4-CD8+) thymocytes. In Ras signaling and proliferation assays, mutant thymocytes showed a complete lack of response to DAG analogs or T cell receptor (TCR) stimulation by antibodies. Thus, TCR and DAG are linked through RasGRP to Ras signaling.
ISSN:1529-2908
1529-2916
DOI:10.1038/79766