Importantly, we demonstrated this negative regulatory activity not only in the leukemic Jurkat T-cell line (which lacks PTEN and SHIP expression), but also in the mouse D10 T-cell line, which expresses both PTEN and SHIP, and has apparently normal regulation of the PI3K pathway. At this point, we believe that at least a part of this activity of PIK3IP1 is due to its ability to dampen signaling through the PI3K pathway, since siRNA-mediated knock-down of PIK3IP1 resulted in enhanced phosphorylation of Akt. Also, this is consistent with a previous study that directly demonstrated inhibition of PI3K by PIK3IP1 [7]. Unlike previously described negative regulators of the PI3K

pathway, PIK3IP1

appears ICG-001 to function further upstream, at the level of PI3K activation itself. Further study will be necessary to determine more precisely the molecular mechanism behind this inhibition, including which isoforms of p110 are inhibited by PIK3IP1 in T cells. In addition, it will be of interest to understand the function of the PIK3IP1 extracellular kringle domain, which may mediate its association with other cell-surface proteins. Finally, our data indicate that further genetic analysis is warranted to more carefully tease out the role of PIK3IP1 in T-cell development and function in vivo. Anti-PIK3IP1 antibody and siRNA specific for human PIK3IP1 were described PD0325901 cost previously [7]. SmartPool siRNA oligos specific for murine PIK3IP1 Chloroambucil were obtained from Dharmacon (Chicago, IL, USA). The additional PIK3IP1 antibody H-180, and antibodies to p110α and p110β and the myc epitope tag were from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Anti-p110δ was from Abcam (Cambridge, MA, USA). Anti-p85 (phospho and total)

antibodies were obtained from Cell Signaling Technology (Danvers, MA, USA). Polyclonal antibody specific for phospho (S473) Akt was obtained from Biosource/Invitrogen (Carlsbad, CA, USA). Antibody to the Jurkat TCR was purified from the C305.2 hybridoma, which was obtained from ATCC (Manassas, VA, USA). Biotinylated antibodies to human and mouse CD28 (10F3 and 37.51, respectively) and mouse CD3 (2C11), as well as streptavidin were from Invitrogen (Carlsbad, CA, USA). Monoclonal antibody to β-actin was from Sigma (St. Louis, MO, USA). mRNA from D10 T cells was isolated with the ArrayGrade mRNA purification kit (SA Biosciences, Frederick, MD, USA). Total RNA was reverse transcribed using the RT2 first strand kit (C-03; SA Biosciences), and 18s rRNA was chosen as the reference gene for normalization. Real-time PCR was performed with a StepOnePlus system (Applied Biosystems; Foster City, CA, USA) using RT2 SYBR Green/ROX qPCR Master Mixes (SA Biosciences). PCR primers were from SA Biosciences.