Confer A W, Simons K R
Am J Vet Res. 1986 Jan;47(1):154-7.
Lipopolysaccharide (LPS) was obtained from Pasteurella haemolytica serotype 1, using phenol-water extraction, and was evaluated for its ability to modify the biological activity of bovine leukocytes. The LPS was not toxic to polymorphonuclear leukocytes (PMN). The LPS preparation had little effect on random migration of PMN or mononuclear leukocytes (MNL), but caused a 2.5- to 3- fold increase in migration of cells within a whole peripheral blood leukocyte preparation. Phagocytosis of [125I]-labeled Staphylococcus aureus by PMN decreased with low (2.5 micrograms/10(6) cells) and high (65 micrograms/10(6) cells) concentrations of LPS and increased with moderate concentrations of LPS (5 to 25 micrograms/10(6) cells). The LPS enhanced nitroblue tetrazolium reduction by PMN. Moderate LPS concentrations (25 to 50 micrograms/10(6) cells) were mitogenic for MNL, whereas high LPS concentrations (300 micrograms/10(6) inhibited [3H]thymidine incorporation by MNL.
采用酚水提取法从溶血巴斯德氏菌1型中获得脂多糖(LPS),并对其改变牛白细胞生物活性的能力进行评估。该LPS对多形核白细胞(PMN)无毒。LPS制剂对PMN或单核白细胞(MNL)的随机迁移影响不大,但可使全外周血白细胞制剂中的细胞迁移增加2.5至3倍。低浓度(2.5微克/10⁶个细胞)和高浓度(65微克/10⁶个细胞)的LPS会使PMN对[¹²⁵I]标记的金黄色葡萄球菌的吞噬作用降低,而中等浓度(5至25微克/10⁶个细胞)的LPS会使其增加。LPS增强了PMN对硝基蓝四氮唑的还原作用。中等浓度的LPS(25至50微克/10⁶个细胞)对MNL有促有丝分裂作用,而高浓度的LPS(300微克/10⁶个细胞)则抑制MNL掺入[³H]胸腺嘧啶核苷。