Schmitz S, Loeffler M, Jones J B, Lange R D, Wichmann H E
Medical Clinic I, LFI-EDV, University of Cologne, Köln, F.R. Germany.
Cell Tissue Kinet. 1990 Sep;23(5):425-42. doi: 10.1111/j.1365-2184.1990.tb01135.x.
Cyclic haemopoiesis in Grey Collie dogs is characterized by stable oscillations in all haemopoietic lineages. It is proposed that in these animals, in contrast to normal animals, the maturation process of haemopoietic (in particular granuloid) cells from the primitive progenitors to the functional cells is characterized by an abnormally strong synchrony. It is conjectured that the marrow maturation time has a very small variance compared with non-cyclic normal dogs. With a mathematical model of haemopoiesis it is shown that small fluctuations are amplified via regular feedback processes such that stable granuloid oscillations are established. Erythroid oscillations are induced indirectly by granuloid feedback to the stem cell pool. The model calculations further show that the synchrony hypothesis of bone marrow maturation can quantitatively explain the following experimental results: (1) the maintenance of stable cycles of granuloid and erythroid bone marrow and blood cells with a period of approximately 14 d; (2) the disappearance of granuloid and erythroid cycles during the administration of the colony stimulating factor rhG-CSF; (3) the reappearance of oscillations when the administration of CSF is discontinued; (4) the cessation of cycles during endotoxin application; and (5) the persistence of cycles during erythroid manipulations (bleeding anaemia, hypoxia, hypertransfusion). We therefore conclude that cyclic haemopoiesis is not caused by a defect in the regulatory control system but by an unusual maturation process.
灰色柯利犬的周期性造血表现为所有造血谱系的稳定振荡。与正常动物相比,这些动物中造血(特别是粒细胞)细胞从原始祖细胞到功能细胞的成熟过程具有异常强烈的同步性。据推测,与非周期性正常犬相比,骨髓成熟时间的方差非常小。通过造血数学模型表明,小波动通过规则反馈过程被放大,从而建立稳定的粒细胞振荡。红细胞振荡是由粒细胞对干细胞池的反馈间接诱导的。模型计算进一步表明,骨髓成熟的同步性假说可以定量解释以下实验结果:(1)粒细胞和红细胞骨髓及血细胞的稳定周期维持,周期约为14天;(2)在给予集落刺激因子rhG-CSF期间,粒细胞和红细胞周期消失;(3)停止给予CSF时振荡重新出现;(4)应用内毒素期间周期停止;(5)在红细胞操作(出血性贫血、缺氧、大量输血)期间周期持续存在。因此,我们得出结论,周期性造血不是由调节控制系统缺陷引起的,而是由异常的成熟过程引起的。