Hammerstrøm J, Unsgaard G
Acta Pathol Microbiol Scand C. 1979 Dec;87(6):381-9.
The effect of E. coli endotoxin (LPS) on human monocytes and peritoneal macrophages (PEC) during in vitro differentiation was studied. Short-term (less than 24 hours) exposure to LPS in concentrations up to 50 microgram/ml did not affect monocyte survival or 51Cr-release, but concentrations of 10 microgram/ml or more reduced monocyte survival when LPS exposure was prolonged to 72 h. Undifferentiated monocytes seemed to be sensitive to this effect. Monocyte and PEC protein synthesis was reduced by nontoxic LPS concentrations in both undifferentiated and differentiated cells. LPS exposure reduced monocyte ingestion and degradation of 125I-labelled Candida albicans, dependent on time and dosage. The induction of monocyte- and PEC-mediated cytoststic activity to tumour cells induced by prolonged in vitro culture was also impaired by LPS. The morphological alterations induced in mononuclear phagocytes by LPS included a changes distribution of cells in the monolayer, changes in membrane structure and apparent reduction of lysosomes. LPS thus interferes adversely with several aspects of human mononuclear phagocyte in vitro differentiation.
研究了大肠杆菌内毒素(LPS)在体外分化过程中对人单核细胞和腹腔巨噬细胞(PEC)的影响。短期(少于24小时)暴露于浓度高达50微克/毫升的LPS不会影响单核细胞的存活或51铬释放,但当LPS暴露延长至72小时时,10微克/毫升或更高的浓度会降低单核细胞的存活。未分化的单核细胞似乎对这种作用敏感。无毒LPS浓度会降低未分化和分化细胞中单核细胞和PEC的蛋白质合成。LPS暴露会降低单核细胞对125I标记的白色念珠菌的摄取和降解,这取决于时间和剂量。LPS还会损害体外长期培养诱导的单核细胞和PEC介导的对肿瘤细胞的细胞毒性活性。LPS在单核吞噬细胞中诱导的形态学改变包括单层细胞分布的变化、膜结构的变化以及溶酶体的明显减少。因此,LPS对人单核吞噬细胞体外分化的多个方面产生不利影响。