Becker S
Cell Immunol. 1984 Mar;84(1):145-53. doi: 10.1016/0008-8749(84)90085-6.
The effect of interferon-alpha (Wellferon) on human monocyte to macrophage maturation in vitro has been investigated. Cell volume and three markers, acid phosphatase, leucine aminopeptidase, and phagocytosis, which increase with maturation, have been studied employing recently developed flow cytofluorometric techniques. The increase in cell volume and in the expression of all three markers was inhibited in a dose-dependent manner in monocyte cultures given 50-300 U/ml of interferon within 2 hr of culture initiation. An initial dose of 300 U/ml of interferon, removed from the cultures after 24 hr, was as effective in inhibiting the development of each of the markers as three 100 U pulses on three consecutive days, and as effective as 300 U interferon left in throughout the culture period. Histogram analysis of marker expression indicated that all monocytes, and not a subpopulation, were affected by the interferon. Cytotoxic activity of freshly isolated monocytes rapidly decayed when the cells were cultured under standard maturation conditions. The addition of interferon to the cultures prevented the loss of this activity while also preventing the development of more mature cells. It appears that maintenance of the cytotoxic state is one influence of interferons; however, it may be that these cells have also been directed toward alternate pathways of macrophage differentiation.
已对α干扰素(惠福仁)在体外对人单核细胞向巨噬细胞成熟的影响进行了研究。利用最近开发的流式细胞荧光测定技术,研究了细胞体积以及随着成熟而增加的三种标志物,即酸性磷酸酶、亮氨酸氨肽酶和吞噬作用。在培养开始后2小时内给予50 - 300 U/ml干扰素的单核细胞培养物中,细胞体积的增加以及所有三种标志物表达的增加均受到剂量依赖性抑制。初始剂量为300 U/ml的干扰素在培养24小时后从培养物中去除,其抑制每种标志物发育的效果与连续三天给予三个100 U脉冲相同,并且与在整个培养期间都保留300 U干扰素的效果相同。标志物表达的直方图分析表明,所有单核细胞而非亚群受到干扰素的影响。当新鲜分离的单核细胞在标准成熟条件下培养时,其细胞毒性活性迅速下降。向培养物中添加干扰素可防止这种活性的丧失,同时还可防止更成熟细胞的发育。看来维持细胞毒性状态是干扰素的一种作用;然而,可能这些细胞也已被导向巨噬细胞分化的替代途径。