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Synchrony of bone marrow proliferation and maturation as the origin of cyclic haemopoiesis
Authors:S Schmitz  M Loeffler  J B Jones  R D Lange†  H E Wichmann‡
Institution:Medical Clinic I, LFJ-EDV, University of Cologne. Köln. F.R. Germany, University of Wuppertal, Wuppertal, F.R. Germany;*Medical Clinic I, LFJ-EDV, University of Cologne. Köln. F.R. Germany, Department of Environmental Practice, College of Veterinary Medicine and University of Wuppertal, Wuppertal, F.R. Germany;†Medical Clinic I, LFJ-EDV, University of Cologne. Köln. F.R. Germany, Department of Medical Biology, University of Tennessee, Tennessee, U.S.A. and University of Wuppertal, Wuppertal, F.R. Germany;‡Medical Clinic I, LFJ-EDV, University of Cologne. Köln. F.R. Germany, Department of Occupational Safety and Environmental Medicine, University of Wuppertal, Wuppertal, F.R. Germany
Abstract:Abstract. 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.
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