Wickramasinghe S N
Alcohol Alcohol. 1985;20(3):299-303.
Studies employing uninduced and dimethylsulphoxide-induced HL60 cells have shown that promyelocytes metabolise ethanol (0.1 mg/ml) to acetate at the rate of 3.9 nmol/10(7) cells/hr and there is a progressive fall in the ethanol-metabolising capacity as promyelocytes mature into neutrophil myelocytes and, eventually, to band forms and neutrophil granulocytes. By contrast, macrophages derived from the treatment of HL60 cells with 1,25 [OH]2 vitamin D3 and from the culture of normal blood monocytes metabolised ethanol to acetate at much higher average rates of 180.1 and 184.7 nmol/10(7) cells/hr. Furthermore, nucleated marrow cell suspensions which were depleted of cells capable of adhering to plastic metabolised ethanol at only one-third the rate shown by non-depleted cell suspensions. The data indicate that neutrophils and their granule-containing precursors contribute relatively little and macrophages contribute substantially to the overall rate of ethanol metabolism by suspensions of nucleated marrow cells. In addition, the considerable capacity of macrophages to metabolise ethanol in vitro raises the possibility that the metabolism of ethanol by these cells in vivo may result in some deleterious effect on surrounding cells and thus, account, at least in part, for ethanol-induced tissue damage.
对未诱导和经二甲亚砜诱导的HL60细胞进行的研究表明,早幼粒细胞以3.9纳摩尔/10⁷细胞/小时的速率将乙醇(0.1毫克/毫升)代谢为乙酸盐,随着早幼粒细胞成熟为中性粒细胞髓细胞,最终成为带状细胞和中性粒细胞,其乙醇代谢能力逐渐下降。相比之下,用1,25[OH]₂维生素D₃处理HL60细胞以及正常血液单核细胞培养产生的巨噬细胞将乙醇代谢为乙酸盐的平均速率要高得多,分别为180.1和184.7纳摩尔/10⁷细胞/小时。此外,去除了能够附着于塑料的细胞的有核骨髓细胞悬液代谢乙醇的速率仅为未去除细胞悬液的三分之一。数据表明,中性粒细胞及其含颗粒的前体细胞对有核骨髓细胞悬液中乙醇代谢的总体速率贡献相对较小,而巨噬细胞贡献很大。此外,巨噬细胞在体外具有相当大的乙醇代谢能力,这增加了这些细胞在体内代谢乙醇可能对周围细胞产生一些有害影响的可能性,因此至少部分解释了乙醇诱导的组织损伤。