Ricin toxin binding subunit B (RTB) is one of the subunits of the ricin protein. RTB has been used as adjuvant, but little is known about its mechanism. In this study, we found that RTB increased not only nitric oxide (NO) release, but also tumor necrosis factor (TNF)-α and interleukin (IL)-6 production in mouse macrophage cell line RAW264.7 cells. They subsequently exhibited enhanced ConA-induced T-cell and LPS-induced B-cell proliferative responses. We also examined the cytokines that were produced from splenocytes following in vitro RTB administration. Increased levels of IL-2, interferon (IFN)-γ and TNF-α were observed, while IL-4 and IL-5 were unaffected. These results demonstrate that recombinant RTB can act on the immune system and activate T-cells by introducing a Th1 immune response. Th1 cells might be the primary cellular target affected by RTB. Our results suggest that the recombinant RTB can promote the activation of macrophages and has a beneficial effect on immunomodulatory activity. 相似文献
CuO–CeO2 (Cu–Ce) catalyst with a CuO/CeO2 mass ratio of 1 prepared by a sol–gel method is used in the CO catalytic oxidation reaction in the actual industrial sulfur-containing atmosphere. At a reaction temperature of 200 °C, the catalyst exhibits quite different stability under sulfur-containing and sulfur-free conditions. When 30 ppm SO2 was added to the feed gas, the Cu–Ce catalyst had an initial CO conversion rate of 100%, gradually decreasing after 26 h, and this catalyst completely deactivated at about 50 h. However, the CO conversion rate of the catalyst under sulfur-free conditions could be nearly maintained at 100% within the measured time range (60 h). The results of IR, Raman, and XPS characterizations proved that the accumulation of cerium sulfate on the Cu–Ce catalyst would cover the active sites of the catalyst, eventually leading to the complete deactivation of the catalyst, which provides favorable evidence for the actual industrial anti-sulfur application.
The present study found that ricin toxicity did not only manifest itself as inhibition of protein synthesis, but also induced apoptosis of immune cells and played an extremely significant role in intestinal injury. In this report, we describe a novel method to estimate binding events occurring on intestinal brush border membranes (BBM) based on SPR technology in an attempt to mimic the real intestinal surface capable of interacting physically and/or actively with certain biological molecules. Combined with HPCE-ESI-MS indentification, we obtained 28 kinds of proteins in BBM that interacted with ricin. 相似文献