Ogawa T, Shimauchi H, Uchida H, Mori Y
Department of Oral Microbiology, Osaka University Faculty of Dentistry, Japan.
Immunobiology. 1996;196(4):399-414. doi: 10.1016/S0171-2985(96)80062-3.
Porphyromonas gingivalis 381 lipid A induced strong mitogenic response in splenic B cells separated from LPS-non-responsive C3H/HeJ mice as well as LPS-responsive C3H/HeN mice, by using a magnetic cell sorting system. The lipid A also exhibited mitogenic activity in splenic T cells. P. gingivalis lipid A induced lower production of interleukin-1 beta (IL-1 beta) in splenic macrophage cultures and exhibited a comparable IL-6 producing activity in splenic B cells of C3H/HeN mice as compared to Escherichia coli-type synthetic lipid A (compound 506) and monophosphoryl lipid A from Salmonella minnesota Re 595 (MLA). Furthermore, P. gingivalis lipid A, but not compound 506 nor MLA, induced low IL-1 beta and high IL-6 production in C3H/HeJ mice. C3H/HeJ T cells in response to P. gingivalis lipid A stimulation resulted in definite IL-2 mRNA and its production, whereas IL-4 response was scarcely active in both C3H/HeN and C3H/HeJ T cells. P. gingivalis lipid A increased tyrosine, serine/threonine phosphorylation of proteins with various major induced bands in splenic B cells of both C3H/HeN and C3H/HeJ mice. Thus, P. gingivalis lipid A stimulated the splenic immunocytes of C3H/HeJ as well as C3H/HeN mice.
牙龈卟啉单胞菌381脂多糖通过使用磁性细胞分选系统,在从对脂多糖无反应的C3H/HeJ小鼠以及对脂多糖有反应的C3H/HeN小鼠分离出的脾脏B细胞中诱导出强烈的促有丝分裂反应。该脂多糖在脾脏T细胞中也表现出促有丝分裂活性。牙龈卟啉单胞菌脂多糖在脾脏巨噬细胞培养物中诱导产生较低水平的白细胞介素-1β(IL-1β),并且与大肠杆菌型合成脂多糖(化合物506)和来自明尼苏达沙门氏菌Re 595的单磷酰脂多糖(MLA)相比,在C3H/HeN小鼠的脾脏B细胞中表现出相当的IL-6产生活性。此外,牙龈卟啉单胞菌脂多糖而非化合物506或MLA,在C3H/HeJ小鼠中诱导产生低水平的IL-1β和高水平的IL-6。对牙龈卟啉单胞菌脂多糖刺激有反应的C3H/HeJ T细胞产生了确定的IL-2 mRNA及其产物,而在C3H/HeN和C3H/HeJ T细胞中IL-4反应几乎没有活性。牙龈卟啉单胞菌脂多糖增加了C3H/HeN和C3H/HeJ小鼠脾脏B细胞中具有各种主要诱导条带的蛋白质的酪氨酸、丝氨酸/苏氨酸磷酸化。因此,牙龈卟啉单胞菌脂多糖刺激了C3H/HeJ以及C3H/HeN小鼠的脾脏免疫细胞。