Multiple mechanisms for TRAF3-mediated regulation of the T cell costimulatory receptor GITR

• Published in: The Journal of biological chemistry 2021-09, Vol.297 (3), p.101097-101097, Article 101097
• Main Authors: Li, Hanzeng, Hostager, Bruce S., Arkee, Tina, Bishop, Gail A.
• Format: Article
• Language: English
• Subjects: adaptor protein; Animals; Costimulatory and Inhibitory T-Cell Receptors - metabolism; Female; GITR; Glucocorticoid-Induced TNFR-Related Protein - metabolism; Glucocorticoid-Induced TNFR-Related Protein - physiology; Interleukin-2 - metabolism; Lymphocyte Activation; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; NF-kappa B - metabolism; receptor; Receptors, Tumor Necrosis Factor - metabolism; signal transduction; Signal Transduction - immunology; T-cell; T-Lymphocytes - metabolism; TNF Receptor-Associated Factor 3 - metabolism; TNF Receptor-Associated Factor 3 - physiology; TRAF
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2021.101097

Tumor necrosis factor receptor (TNFR)-associated factor 3 (TRAF3) plays context-specific roles in multiple receptor-mediated signaling pathways in different cell types. Mice lacking TRAF3 in T cells display defective T-cell-mediated immune responses to immunization and infection and demonstrate defective early signaling via the TCR complex. However, the role of TRAF3 in the function of GITR/TNFRSF18, an important costimulatory member of the TNFR superfamily, is unclear. Here we investigated the impact of T cell TRAF3 status on both GITR expression and activation of specific kinases in the GITR signaling pathway in T cells. Our results indicate that TRAF3 negatively regulates GITR functions in several ways. First, expression of GITR protein was elevated in TRAF3-deficient T cells, resulting from both transcriptional and posttranslational regulation that led to greater GITR transcript levels, as well as enhanced GITR protein stability. TRAF3 associated with T cell GITR in a manner dependent upon GITR ligation. TRAF3 also inhibited several events of the GITR mediated early signaling cascade, in a manner independent of recruitment of phosphatases, a mechanism by which TRAF3 inhibits signaling through several other cytokine receptors. These results add new information to our understanding of GITR signaling and function in T cells, which is relevant to the potential use of GITR to enhance immune therapies.