01% Tween 20/PBS for 30 min. Subsequently, cells were incubated with fluorochrome-conjugated secondary antibodies [Ax488 goat anti-mouse IgG1/2a, Ax546 goat anti-mouse IgG1, Ax546 goat anti-rabbit IgG, Ax546 donkey anti-goat IgG (Invitrogen)] in 2% BSA/0.01% Tween 20/PBS

for 30 min and mounted using DakoCytomation mounting medium. Imaging was performed using a Zeiss EX-527 LSM 510 META confocal microscope equipped with a 63 × /1.4 NA oil-immersion objective and an AxioCam HR (Carl Zeiss, Göttingen, Germany), using laser excitation at 488, 561 and 633 nm. DPC localization was evaluated as the area fraction of fluorescent pixels at the DPC relative to total area of fluorescent pixels for the cell/bead conjugate https://www.selleckchem.com/products/PD-0325901.html using the image analysis software ImageJ developed by Wayne Rasband, National Institute of Health, Bethesda, MD, USA. Graphs were made in SigmaPlot 8.0 (SPSS, Chicago, IL, USA). Statistical analyses were performed using the Mann–Whitney U-test, conducted in spss 16.0 for Windows (Chicago, IL, USA). Upon sustained T cell activation, maintained type II PKA association with the centrosome and the microtubule organizing centre [16] and redistribution of type I PKA (in mouse T cells) [17] have been described. Additionally, type I PKA localization has been observed at the IS and at the DPC of primary human T cells activated by SEB-pulsed Raji B cells [5]. We found type

I PKA [regulatory subunit (R)Iα] to mainly localize with filamentous

(F)-actin close to the cell membrane in resting primary human T cells (Fig. 1B, upper panel). Upon activation with CD3/CD28-coated beads, F-actin accumulated at the cell/bead contact zone, a known hallmark of productive TCR engagement alongside reorientation of the microtubule organizing centre identified here by β-tubulin staining (Fig. 1A, [3]). The accumulation intensified and persisted for at least 20 min (Fig. 1B, left column, Interleukin-3 receptor and A) and was used as a marker for activated conjugates. About 1 min after activation, RIα was recruited to the IS, then distributed back in the membrane at 5 min before translocating to the distal pole (DP) of the cell (20 min) (Fig. 1B, middle column). After 20 min, RIα was localized at the DP in 69 ± 4% of activated T cells (mean ± SEM, n = 100 T cells from each of three donors). Thus, CD3/CD28-coated beads robustly and reproducibly generated a high percentage of activated T cells, in which RIα was consistently found to migrate via the IS to the DP. To align cross-ligation with CD3/CD28-coated beads with a more physiological mode of activation, we stimulated primary human T cells for 30 min with SE-primed Raji B cells (Fig. 1C). In successfully activated T cells (31 ± 10% of the conjugates, mean ± SEM, n = 100 T cells from each of two donors), CD3 accumulated at the IS at the T cell/Raji B cell interface (Fig. 1C, left column).