Essential function for the GTPase TC21 in homeostatic antigen receptor signaling
doi: 10.1038/ni.1749
pmid: 19561613
Essential function for the GTPase TC21 in homeostatic antigen receptor signaling
T cell antigen receptors (TCRs) and B cell antigen receptors (BCRs) transmit low-grade signals necessary for the survival and maintenance of mature cell pools. We show here that TC21, a small GTPase encoded by Rras2, interacted constitutively with both kinds of receptors. Expression of a dominant negative TC21 mutant in T cells produced a rapid decrease in cell viability, and Rras2(-/-) mice were lymphopenic, possibly as a result of diminished homeostatic proliferation and impaired T cell and B cell survival. In contrast, TC21 was overexpressed in several human lymphoid malignancies. Finally, the p110delta catalytic subunit of phosphatidylinositol-3-OH kinase (PI(3)K) was recruited to the TCR and BCR in a TC21-dependent way. Consequently, we propose TC21 directly links antigen receptors to PI(3)K-mediated survival pathways.
B-Lymphocytes, Lymphoma, B-Cell, Cell Survival, T-Lymphocytes, Receptors, Antigen, T-Cell, Membrane Proteins, Receptors, Antigen, B-Cell, Lymphoma, T-Cell, Mice, Phosphatidylinositol 3-Kinases, Animals, Homeostasis, Humans, Lymph Nodes, Monomeric GTP-Binding Proteins, Signal Transduction
B-Lymphocytes, Lymphoma, B-Cell, Cell Survival, T-Lymphocytes, Receptors, Antigen, T-Cell, Membrane Proteins, Receptors, Antigen, B-Cell, Lymphoma, T-Cell, Mice, Phosphatidylinositol 3-Kinases, Animals, Homeostasis, Humans, Lymph Nodes, Monomeric GTP-Binding Proteins, Signal Transduction
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