Nagai H, Ueno M, Hirashima M
Department of Pathology, Kumamoto University Medical School, Japan.
Int Arch Allergy Immunol. 1994;104 Suppl 1(1):12-4. doi: 10.1159/000236738.
Effects of lipopolysaccharides (LPS) on the production of chemotactic lymphokines for eosinophils and monocytes (ECF and MCF) from antigen- or mitogen-stimulated T cells were examined. Supernatants from monocytes stimulated with various LPS regulated concanavalin A (Con A)- and purified protein derivative (PPD)-induced ECF or MCF production. The regulation varied with LPS used for monocyte stimulation. The supernatant from monocytes stimulated with LPS from Escherichia coli, J-5 strain, selectively potentiated ECF production, whereas that from Salmonella minesota potentiated MCF production. In contrast, supernatant from monocytes stimulated with LPS from Salmonella typhimurium potentiated both ECF and MCF production, whereas that from Vibrio cholerae failed to potentiate production. The supernatants from monocytes stimulated with lipid A of S. typhimurium, S. minesota, and E. coli, however, failed to potentiate ECF and MCF production. The potentiating activity for each lymphokine was recovered from fractions ranging in molecular weight between 10 and 20 kD. Further purification with isoelectric electrophoresis revealed that the potentiating activity for the production of chemotactic lymphokine for eosinophils has a pI value of about 4-5, and that the activity for MCF production is detected in two fractions of pI about 5-6, and 7-8. Macrophage lineage cell line cells, such as THP-1 and U-937, also release similar factors after differential stimulation.
研究了脂多糖(LPS)对抗原或丝裂原刺激的T细胞产生嗜酸性粒细胞和单核细胞趋化性淋巴因子(ECF和MCF)的影响。用各种LPS刺激单核细胞产生的上清液可调节伴刀豆球蛋白A(Con A)和纯化蛋白衍生物(PPD)诱导的ECF或MCF产生。这种调节因用于刺激单核细胞的LPS不同而异。用大肠杆菌J-5株的LPS刺激单核细胞产生的上清液选择性地增强了ECF的产生,而用明尼苏达沙门氏菌的LPS刺激单核细胞产生的上清液则增强了MCF的产生。相比之下,用鼠伤寒沙门氏菌的LPS刺激单核细胞产生的上清液增强了ECF和MCF的产生,而用霍乱弧菌的LPS刺激单核细胞产生的上清液则未能增强其产生。然而,用鼠伤寒沙门氏菌、明尼苏达沙门氏菌和大肠杆菌的脂多糖A刺激单核细胞产生的上清液未能增强ECF和MCF的产生。每种淋巴因子的增强活性可从分子量在10至20 kD之间的组分中回收。通过等电聚焦进一步纯化表明,嗜酸性粒细胞趋化性淋巴因子产生的增强活性的pI值约为4 - 5,而MCF产生的活性在pI约为5 - 6和7 - 8的两个组分中检测到。巨噬细胞系细胞系,如THP-1和U-937,在差异刺激后也释放类似的因子。