In contrast, Tax2 protein does not contain NF-κB2 domain, does not bind p100, and therefore does not induce its processing to the active p52 subunit [19, 20]. Tax1, but not Tax2, has

been found to have a co-operative role with the non-canonical NF-κB pathway to mediate T cell transformation and leukaemogenesis [23]. Recently our group reported that extracellular Tax1 and Tax2 proteins induce the expression of macrophage inflammatory protein (MIP)-1α/CCL3, MIP-1β/CCL4 and regulated upon activation normal T cell expressed and secreted (RANTES)/CCL5 from peripheral blood mononuclear cells (PBMCs) and monocyte-derived macrophages (MDMs) [24, 25] with the concomitant down-regulation of CCR5, the HIV-1 co-receptor [24]. Additionally Tax1 and Tax2 expressed via adenoviral vectors delivered into MDMs also induced the secretion of CC-chemokines [25]. Fostamatinib CC-chemokines have been correlated with innate resistance to HIV-1 infection, decreased viral loads in individuals already infected and protection against disease progression to AIDS [26]. We have hypothesized that Tax2 has the potential to alter innate Buparlisib manufacturer host immune responses

and may be capable of modifying HIV-1 pathogenesis in HIV-1/HTLV-2 co-infected individuals. In this study we aimed to investigate whether or not Tax2 could induce the expression of CC-chemokines in cultured PBMCs through the canonical NF-κB signalling pathway. The effect of potent inhibitors of the canonical NF-κB signalling was examined to determine whether CC-chemokine production is dependent upon this pathway. Blood samples from three HIV-1 and HTLV-1/-2 seronegative donors were obtained following informed consent using a protocol that was approved by the Institutional Review Board for Human Investigation of the Milwaukee Veterans Affairs, Research Service Committee. Whole blood was collected in CPT/Vacutainer BD tubes (BD Biosciences, San Jose, CA,

USA) and PBMCs were obtained following the manufacturer’s instructions. Phorbol 12-myristate 13-acetate (PMA at 50 ng/ml; Sigma, St Louis, MO, USA) and phytohaemagglutinin (PHA at 5 μg/ml; Sigma) were used to stimulate PBMCs. The NF-κB inhibitor pyrrolidine dithiocarbamate was used to pretreat Baricitinib PBMCs (PDTC at 30 μM; Sigma). Antibodies specific for phospho-p65/RelA (Ser536) were from Cell Signaling Technology and fluorescein isothiocyanate (FITC)-labelled goat anti-rabbit immunoglobulin (Ig)G (H + L), F(ab′)2 was obtained from KPL Inc. (Gaithersburg, MD, USA). The HTLV-2-infected human T cell line (known as MoT, ATCC CRL-8086) expresses Tax2 and mature HTLV-2 viral particles and exhibits constitutive activation of NF-κB [27]. MoT cells, used as positive control, were grown in complete RPMI medium [RPMI medium supplemented with 10% fetal bovine serum (FBS), 2·05 mM L-glutamine, 1% penicillin/streptomycin (P/S v/v), 1% sodium pyruvate (v/v)] and cultured in a humidified incubator at 37°C with 5% CO2.