G41, using quantitative real-time RT-PCR. Thus, as shown in Fig. 1B, PIK3IP1 message was detected in these cells, and stimulation

with anti-CD3/CD28 antibodies led to a transient decrease in this mRNA, relative to the control (18S rRNA). We next sought to confirm that PIK3IP1 is also present at the protein level in T cells. Lysates from the Jurkat human T-cell line, as well as primary murine T cells, both naïve and activated, were analyzed by western blotting for expression of PIK3IP1 and other members of the PI3K pathway, using a previously described antibody [7]. As shown in Fig. 1C, PIK3IP1 protein was detected in all T cells with particularly high levels in the human leukemic T-cell line Jurkat. The latter is intriguing, since Jurkat cells were previously described as lacking expression two other regulators

of the PI3K pathway, the lipid phosphatases PTEN and SHIP selleck [10, 11]. We confirmed the expression of PIK3IP1 at the protein by western blotting with a different antibody (H-180, from www.selleckchem.com/products/VX-809.html Santa Cruz Biotechnology). Thus, as shown in Fig. 1D, this antibody also detected PIK3IP1 in lysates of Jurkat T cells, as well as the mouse T-cell clone D10 and naïve CD3+ T cells freshly isolated from mouse spleen and lymph node. Since PIK3IP1 has been characterized as a negative regulator of the PI3K pathway in other cell types [7], we hypothesized that altered levels of PIK3IP1 expression might modulate signaling pathways that regulate T-cell activation. We first investigated the effects of ectopic PIK3IP1 expression. T-cell activation and effector function are critically regulated by the transcription factors

NF-κB, NFAT, and AP-1, the latter two of which often bind in tandem to composite elements Sorafenib in genes like that encode IL-2. Thus, transfection of a myc-tagged PIK3IP1 construct into D10 T cells, a murine Th2 T-cell line that expresses normal levels of both PTEN and SHIP [12], led to a dose-dependent decrease in the activation of an NFAT/AP-1 transcriptional reporter (Fig. 2A). This inhibition was evident in response to stimulation with anti-TCR/CD28 antibodies or the pharmacological agents PMA and ionomycin. We also examined the effects of ectopic PIK3IP1 expression on the NF-κB pathway, and although statistically significant inhibition was observed at the highest concentration of PIK3IP1 transfection, less dramatic results were observed with an NF-κB reporter (Fig. 2B). Transfected PIK3IP1 was detected with an antibody to the myc epitope tag (Fig. 2C) or with an antibody to total PIK3IP1 (Fig. 2D). The latter revealed overexpression in the range of 2–3-fold over endogenous protein. Ectopic expression of PIK3IP1 had no apparent broad effects on transfection efficiency or viability, as determined by the expression of a constitutively expressed GFP reporter (Fig. 2E), which was co-transfected with the NFAT/AP-1 or NF-κB transcriptional reporters.