However, the scaffold proteins specific for TCR-mediated JNK1 activation is less clear. The TCR connects

to JNK activation through the guanine exchange factor Vav1 and the adaptor/guanine exchange factor complex, Grb2/SOS. These molecules are recruited to phosphorylated tyrosine residues on the linker for activation of T cells (LAT) [1]. Importantly, both Vav1 and Grb2/SOS activate Rac1 and deficiencies in either lead to significant reduction in JNK signaling [29, 30]. POSH was initially identified as a scaffold protein that linked active Rac1 to JNK and NF-κB activation [26], while JIP-1 is a scaffold that facilitates JNK activation through the recruitment of MLK and MKK7 [25]. Interestingly, in neurons, the association

of POSH and JIP-1 mediates JNK activation MI-503 purchase and apoptosis [31, 32]. However, the role of POSH and JIP-1 in TCR-dependent JNK activation is not known. Here, we investigated the role of POSH in JNK activation in CD8+ T cells. Using a peptide inhibitor strategy, we determined that the interaction between POSH and JIP-1 is required for JNK1, but not JNK2, phosphorylation, and T-cell effector function. Most interestingly, the disruption of the POSH/JIP-1 complex results in functional defects that phenocopy JNK1−/− T cells. Uncoupling POSH and JIP-1 resulted in decreased proliferation, defects in IFN-γ and TNF-α expression, and markedly selleck chemicals reduced tumor clearance. Correspondingly, the POSH/JIP-1 regulation of JNK1 was also important for the induction of the transcription factors c-Jun, T-bet, and Eomesodermin (Eomes), which play important roles in programing effector function. Collectively,

these data indicate for the first time that POSH and the POSH/JIP-1 scaffold network are specifically required for JNK1-dependent Urocanase T-cell differentiation and effector function in mature CD8+ T cells. POSH is a Rac1-dependent scaffold of JNK signaling [26]. To identify a role for POSH in TCR-mediated JNK activation, we established its ability to bind components of the JNK signaling cascade in CD8+ T cells. For this, OT-1 TCR transgenic blasts (CTLs) were restimulated with OVA-tetramer (Tet)/α-CD28 and subjected to immunoprecipitation (IP) with antibodies against Rac1. Co-IP of components of the JNK signaling pathway was assessed by immunoblot. POSH, JIP-1, JNK, and MKK7 were all found in complex with Rac1 (Fig. 1A, data not shown). Interestingly, pulldowns of GTP-bound (active) Rac1 indicated that the association of POSH and JNK increased with JNK activation (Fig. 1B). Given the importance of JNK in regulating T-cell differentiation, we also wished to assess the association of these molecules in naïve cells. However, naïve cells have low expression of POSH, JIP-1, and JNK [21], which greatly reduces the ability to detect their association by classic IP.