Since PCT also presents two/three relevant polycationic motifs, c

Since PCT also presents two/three relevant polycationic motifs, comparable to some of the physical-chemical patterns of such antimicrobial peptides previously studied, we investigated the in vitro interaction between PCT and both rough and smooth chemotype LPS

[7] by limulus amoebocyte lysate (LAL) test. As PCT was able to significantly decrease LAL assay reactivity Crenigacestat molecular weight in both LPSs tested, the effects of PCT-pre-incubated LPS on the release of cytokines in human peripheral blood mononuclear cells (PBMC) were examined. For this purpose, the mononuclear cell targeting chemokine (MCP-1), as well as Th1, Th2 and Treg type cytokines were selected. Results LPS-neutralizing activity of PCT Following incubation of different concentrations of PCT with LPS for 30 minutes, PCT at a concentration of 500 pg/ml, significantly decreased the LAL reactivity of 100 pg/ml of both GSK2879552 chemical structure the rough LPS chemotype (S. typhimurium LPS, p = 0.0010) and the smooth LPS chemotype (E. coli LPS, p = 0.0030) (Figure 1). Higher (5000 pg/ml) (Figure 1) or lower (50 pg/ml) (data not shown), concentrations of PCT did not produce any significant change in LAL reactivity of the LPS assessed. Figure

1 Neutralization by PCT of LPS from S. typhimurium and E. coli . The effect of PCT on S. typhimurium and E. coli LPS (100 pg/ml) reactivity was evaluated as O. D. (405 nm) by the chromogenic LAL test after 30 minutes incubation of the above reported LPS concentration: with 0 pg/ml PCT (LPS 30 min), with 5000 pg/ml PCT (LPS + PCT 5000 30 min), 500 pg/ml PCT (LPS + PCT 500 30 min). Results are Beta adrenergic receptor kinase presented as means ± SEM of at least four experiments each carried out in duplicate. Statistical significance between groups was assessed by Student’s t test. A p < 0.05 was considered significant,

whereas not significant (n.s.) difference was associated with a p ≥ 0.05. Statistics were performed in comparison with respective LPS type-stimulated PCT-untreated cells (LPS 30 min), and the exact significance index is indicated on the top of the horizontal line encompassing the two statistically compared bars. PCT effects on LPS-induced cytokine release After 4 and 24 hours incubation of human PBMC with S. typhimurium LPS pre-incubated with PCT, the release of TNFα, IL-10, IL-4 and MCP-1 was simultaneously assessed with a cytokine biochip array. LPS in RPMI 1640 medium in the absence of PCT induced a substantial increase of all the cytokines evaluated in human PBMC at both time points of 4 and 24 hours as expected. When LPS was pre-incubated with PCT at different concentrations, a decrease of the TNFα release was observed for both time points, this reduction was concentration-dependent at 4 hours (Figure 2). The LPS-induced release of TNFα after 4 hours of incubation was significantly reduced by 500 ng/ml (p = 0.0453) and by 5000 ng/ml (p = 0.

Comments are closed.