Tufano M A, Rossano F, Catalanotti P, Liguori G, Capasso C, Ceccarelli M T, Marinelli P
Istituto di Microbiologia, Seconda Università di Napoli, Italy.
Infect Immun. 1994 Apr;62(4):1392-9. doi: 10.1128/iai.62.4.1392-1399.1994.
Studies were carried out on some biological activities of Helicobacter pylori porins in vitro. We extracted and purified a porin with an apparent molecular mass of 30 kDa. Human polymorphonuclear leukocytes preincubated with H. pylori porins showed a decrease of chemotaxis, of adherence to nylon wool, and of chemiluminescence. Used as chemotaxins in place of zymosan-activated serum or as chemotaxinogens in place of zymosan, the porins induced polymorphonuclear leukocyte migration. Human monocytes and lymphocytes cultivated in the presence of H. pylori porins released cytokines. Release of the various cytokines studied was obtained with differentiated kinetics and at various porin concentrations. Starting only 3 h after culture, tumor necrosis factor alpha is released quickly, reaching a peak at 18 h, at a porin concentration of 1 microgram/ml/10(6) cells. Interleukin-6 (IL-6) appears later, with a peak at 10 micrograms/ml/10(6) cells, while IL-8 is released after 6 h of culture, with a peak at 24 h, at a porin concentration of 10 micrograms/ml/10(6) cells, while IL-8 is released after 6 h of culture, with a peak at 24 h, at a porin concentration of 10 micrograms/ml/10(6) cells. Lymphocytes stimulated by H. pylori porins release gamma interferon after 18 h of culture at higher concentrations of porins (20 micrograms/ml/10(6) cells). Granulocyte macrophage colony-stimulating factor is released from 6 to 48 h at a concentration of 1 microgram/ml/10(6) cells, while both IL-3 and IL-4 are released after 18 h of culture at different porin concentrations (0.1 and 1 microgram/ml/10(6) cells, respectively). Our results lead us to think that during H. pylori infection, surface components, porins in particular, are able to induce a series of chain reactions ranging from the inflammatory to the immunological responses.
对幽门螺杆菌孔蛋白的一些体外生物学活性进行了研究。我们提取并纯化了一种表观分子量为30 kDa的孔蛋白。预先与幽门螺杆菌孔蛋白孵育的人多形核白细胞表现出趋化性、对尼龙毛的黏附性及化学发光的降低。孔蛋白用作趋化因子替代酵母聚糖激活血清或用作趋化因子原替代酵母聚糖时,可诱导多形核白细胞迁移。在幽门螺杆菌孔蛋白存在的情况下培养的人单核细胞和淋巴细胞会释放细胞因子。所研究的各种细胞因子的释放具有不同的动力学且在不同的孔蛋白浓度下出现。仅在培养3小时后,肿瘤坏死因子α迅速释放,在18小时达到峰值,孔蛋白浓度为1微克/毫升/10⁶个细胞。白细胞介素-6(IL-6)出现较晚,在10微克/毫升/10⁶个细胞时达到峰值,而IL-8在培养6小时后释放,在24小时达到峰值,孔蛋白浓度为10微克/毫升/10⁶个细胞,而IL-8在培养6小时后释放,在24小时达到峰值,孔蛋白浓度为10微克/毫升/10⁶个细胞。在较高孔蛋白浓度(20微克/毫升/10⁶个细胞)下培养18小时后,受幽门螺杆菌孔蛋白刺激的淋巴细胞释放γ干扰素。粒细胞巨噬细胞集落刺激因子在6至48小时以1微克/毫升/10⁶个细胞的浓度释放,而IL-3和IL-4在培养18小时后在不同的孔蛋白浓度(分别为0.1和1微克/毫升/10⁶个细胞)下释放。我们的结果使我们认为在幽门螺杆菌感染期间,表面成分,尤其是孔蛋白,能够引发一系列从炎症反应到免疫反应的连锁反应。