Metcalf D, Lindeman G J, Nicola N A
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.
Blood. 1995 May 1;85(9):2364-70.
An unusual mouse line (max 41) that carries an inserted transgene encoding the nuclear transcription factor, Max, exhibits a 50- to 60-fold elevation of blood neutrophils and a 10-fold elevation of blood monocytes. Analysis showed that these elevated levels of blood cells were sustained incrementally by a sevenfold increase in mature neutrophils in the bone marrow and spleen and a fourfold increase in granulocyte-committed progenitor cells with normal turnover times for mature neutrophils and monocytes in the marrow and blood. the progenitor cells were not autonomous and exhibited a normal quantitative responsiveness to stimulation in vitro by the four colony-stimulating factors. A consistent anomaly noted was that, when stimulated by macrophage colon-stimulating factor, max 41 progenitor cells formed mainly granulocyte-containing colonies, rather than the usual macrophage colonies. The blast colony-forming cells from max 41 mice did not generate abnormal numbers or types of progenitor cells. The transgenic max 41 model requires further analysis to establish the regulatory anomaly responsible for the excessive production of granulocytes and monocytes, but has emphasized that most neutrophils generated in the marrow normally never leave the organ.
一种携带插入的编码核转录因子Max的转基因的异常小鼠品系(max 41),其血液中性粒细胞升高50至60倍,血液单核细胞升高10倍。分析表明,这些血细胞水平的升高是由骨髓和脾脏中成熟中性粒细胞增加7倍以及粒细胞定向祖细胞增加4倍持续递增维持的,骨髓和血液中成熟中性粒细胞和单核细胞的周转时间正常。祖细胞并非自主的,并且对四种集落刺激因子的体外刺激表现出正常的定量反应性。一个持续存在的异常情况是,当受到巨噬细胞集落刺激因子刺激时,max 41祖细胞主要形成含粒细胞的集落,而不是通常的巨噬细胞集落。来自max 41小鼠的原始集落形成细胞不会产生异常数量或类型的祖细胞。转基因max 41模型需要进一步分析以确定导致粒细胞和单核细胞过度产生的调节异常,但已强调骨髓中产生的大多数中性粒细胞通常不会离开该器官。