Ross D D, Pollak A, Akman S A, Bachur N R
Laboratory of Clinical Biochemistry, Baltimore Cancer Research Program, DCT, NCI, NIH, 655 West Baltimore Street, Baltimore, MD 21201, USA.
Exp Hematol. 1980 Aug;8(7):954-60.
We investigated whether human circulating myeloid progenitor cells (CFU(c)) exhibit diurnal variation. Peripheral venous blood samples were drawn every 3 h from each of the nine healthy male volunteers. Blood mononuclear cells were harvested by the Ficoll-Hypaque method. CFU(c) content of blood was determined by the soft agar cloning assay. Human placental conditioned medium (HPCM) was used as colony stimulating factor. We found a 24 h cyclic variation of colonies/10(5) mononuclear cells plated with a maximum at 9 a.m. (P < 0.01). Analysis of the colonies by in situ staining indicated that this variation could be attributed almost entirely to colonies composed of eosinophilic cells (representative of CFU(eos)). Neutrophil/macrophage colonies (representative of CFU(G,M)) exhibited a trend toward a 9 a.m. maximum, but this variation was not statistically significant. We conclude that time of blood collection should be standardized in experiments measuring human peripheral blood CFU(c).
我们研究了人类循环髓系祖细胞(CFU(c))是否呈现昼夜变化。从9名健康男性志愿者身上每隔3小时采集一次外周静脉血样本。采用Ficoll-Hypaque法收集血液单核细胞。通过软琼脂克隆试验测定血液中的CFU(c)含量。用人胎盘条件培养基(HPCM)作为集落刺激因子。我们发现每10(5)个接种的单核细胞中集落数存在24小时周期性变化,上午9点达到峰值(P < 0.01)。通过原位染色对集落进行分析表明,这种变化几乎完全归因于由嗜酸性细胞组成的集落(代表CFU(eos))。中性粒细胞/巨噬细胞集落(代表CFU(G,M))呈现出上午9点达到峰值的趋势,但这种变化无统计学意义。我们得出结论,在测量人类外周血CFU(c)的实验中,采血时间应标准化。