Tufano M A, Berlingieri M T, Sommese L, Galdiero F
Microbiologica. 1984 Oct;7(4):353-66.
In this study, we describe the role of porins extracted from the outer membrane of S. typhimurium on the interaction with the host organism. The tests were performed on CD-1 mice immunized both with whole S. typhimurium cells and with purified porins. The antibody titres obtained in mice treated with purified porins and in those treated with whole Salmonella are 1/320 and 1/80 respectively. Cell-mediated response was found to be stimulated in both mice groups: our results show that T lymphocytes determine an increase in H3-thymidine incorporation and MIF production. An increase in lymphocytes with membrane immunoglobulins was observed in the lymphocyte population from the spleens of the treated mice. Purified porins added to macrophages cultures exerted a toxic effect at concentrations between 10 and 20 micrograms/ml. Subinhibiting concentrations (5 micrograms/ml) led to modifications in the surface tension of macrophages layers adhering to the slides. Moreover, subinhibiting porins concentrations were found to modify macrophage functionality as shown by evaluation of the phagocytic index and of intracellular killing, both of which were found to have diminished with respect to controls. When purified porins were added in vitro to populations enriched with T and B lymphocytes, at concentrations between 1 and 5 micrograms/ml they were found to be mitogenic with respect to B lymphocytes. The results we obtained showed that lymphocytes with IgM increase in porins tests. Eventually, purified porins added to Hela and Hep-2 cells were shown to exert a toxic effect which became detectable in the final concentration of 5 micrograms/ml and 1 micrograms/ml for Hela and Hep-2 cells respectively.
在本研究中,我们描述了从鼠伤寒沙门氏菌外膜提取的孔蛋白在与宿主生物体相互作用中的作用。对用完整鼠伤寒沙门氏菌细胞和纯化孔蛋白免疫的CD - 1小鼠进行了测试。用纯化孔蛋白处理的小鼠和用完整沙门氏菌处理的小鼠获得的抗体滴度分别为1/320和1/80。发现两组小鼠的细胞介导反应均受到刺激:我们的结果表明,T淋巴细胞可导致H3 - 胸腺嘧啶核苷掺入量增加和巨噬细胞移动抑制因子(MIF)产生增加。在处理过的小鼠脾脏淋巴细胞群体中观察到带有膜免疫球蛋白的淋巴细胞增加。添加到巨噬细胞培养物中的纯化孔蛋白在浓度为10至20微克/毫升时发挥毒性作用。亚抑制浓度(5微克/毫升)导致附着在载玻片上的巨噬细胞层表面张力发生改变。此外,如通过吞噬指数和细胞内杀伤评估所示,发现亚抑制浓度的孔蛋白会改变巨噬细胞功能,相对于对照组,这两项指标均有所下降。当在体外将纯化孔蛋白添加到富含T和B淋巴细胞的群体中时,发现其在浓度为1至5微克/毫升时对B淋巴细胞具有促有丝分裂作用。我们获得的结果表明,在孔蛋白测试中带有IgM的淋巴细胞增加。最终,添加到Hela细胞和Hep - 2细胞中的纯化孔蛋白显示出毒性作用,分别在Hela细胞终浓度为5微克/毫升和Hep - 2细胞终浓度为1微克/毫升时可检测到。