Johnson E, Bögwald J, Seljelid R
Scand J Immunol. 1982 Dec;16(6):525-30. doi: 10.1111/j.1365-3083.1982.tb00754.x.
Agarose stimulation of macrophages in vitro was studied. Under conditions where agarose was ingested, stimulation was detected during 24-48 h of incubation at a time when the agarose increasingly was concentrated in the perinuclear region. Removal of extracellular agarose after 24 h when endocytosis had reached a plateau did not reduce the stimulatory effect. Preincubation for 4 days with dextran sulphate in concentrations reported to inhibit phagosome-lysosome fusion potentiated strongly the stimulatory effect. In all situations in which agarose was not internalized--in teflon tubes where the cells remain in suspension, on glass cover slips with inhibitors (2-deoxy-D-glucose, cytochalasin B), or with large, noningestible Sepharose beads--no stimulation was recorded. The possibility is discussed that stimulation of macrophages by agarose may be related to complement activation in phagosomes.
研究了体外琼脂糖对巨噬细胞的刺激作用。在琼脂糖被摄取的条件下,在孵育24 - 48小时期间检测到刺激,此时琼脂糖越来越多地集中在核周区域。当内吞作用达到平台期后,在24小时去除细胞外琼脂糖并不会降低刺激作用。用据报道可抑制吞噬体-溶酶体融合的浓度的硫酸葡聚糖预孵育4天,强烈增强了刺激作用。在所有琼脂糖未被内化的情况下——在细胞保持悬浮的聚四氟乙烯管中、在含有抑制剂(2 - 脱氧 - D - 葡萄糖、细胞松弛素B)的玻璃盖玻片上,或与大的、不可摄取的琼脂糖珠一起——未记录到刺激。讨论了琼脂糖对巨噬细胞的刺激可能与吞噬体中的补体激活有关的可能性。