Literature DB >> 1700930

Synchrony of bone marrow proliferation and maturation as the origin of cyclic haemopoiesis.

S Schmitz1, M Loeffler, J B Jones, R D Lange, H E Wichmann.   

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.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1700930     DOI: 10.1111/j.1365-2184.1990.tb01135.x

Source DB:  PubMed          Journal:  Cell Tissue Kinet        ISSN: 0008-8730


  9 in total

1.  Modelling human granulopoiesis under poly-chemotherapy with G-CSF support.

Authors:  M Scholz; C Engel; M Loeffler
Journal:  J Math Biol       Date:  2004-12-20       Impact factor: 2.259

2.  The impact of time delays on the robustness of biological oscillators and the effect of bifurcations on the inverse problem.

Authors:  Nicole Radde
Journal:  EURASIP J Bioinform Syst Biol       Date:  2008-11-19

3.  Understanding, treating and avoiding hematological disease: better medicine through mathematics?

Authors:  David C Dale; Michael C Mackey
Journal:  Bull Math Biol       Date:  2014-09-12       Impact factor: 1.758

4.  Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide.

Authors:  John H Baird; Caterina P Minniti; Jung-Min Lee; Xin Tian; Colin Wu; Mary Jackson; Shoaib Alam; James G Taylor; Gregory J Kato
Journal:  Br J Haematol       Date:  2014-11-06       Impact factor: 6.998

5.  Progenitor cell self-renewal and cyclic neutropenia.

Authors:  D Dingli; T Antal; A Traulsen; J M Pacheco
Journal:  Cell Prolif       Date:  2009-04-21       Impact factor: 6.831

6.  A mathematical approach to benzo[a]pyrene-induced hematotoxicity.

Authors:  S Scheding; M Loeffler; V Anselstetter; H E Wichmann
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

Review 7.  Dynamic hematological disease: a review.

Authors:  Catherine Foley; Michael C Mackey
Journal:  J Math Biol       Date:  2008-03-04       Impact factor: 2.259

8.  Personalising docetaxel and G-CSF schedules in cancer patients by a clinically validated computational model.

Authors:  O Vainas; S Ariad; O Amir; W Mermershtain; V Vainstein; M Kleiman; O Inbar; R Ben-Av; A Mukherjee; S Chan; Z Agur
Journal:  Br J Cancer       Date:  2012-07-19       Impact factor: 7.640

9.  A combined model of human erythropoiesis and granulopoiesis under growth factor and chemotherapy treatment.

Authors:  Sibylle Schirm; Christoph Engel; Markus Loeffler; Markus Scholz
Journal:  Theor Biol Med Model       Date:  2014-05-26       Impact factor: 2.432

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.