Compensatory splenic hemopoiesis in beta-thalassemic mice

Exp Hematol. 1993 Feb;21(2):350-3.

Abstract

beta-Thalassemic mice, homozygous for the deletion of the beta major-globin gene, were investigated for compensatory hemopoiesis in bone marrow and spleen. Apart from characteristic severe anemia, these mice have a marked granulocytosis, monocytosis and lymphocytosis. A large compensatory expansion of late (CFU-E) erythroid progenitor cells was demonstrated, predominantly in the spleen. Immature hemopoietic cells (CFU-S) were also expanded, as were early progenitor cells of erythroid (BFU-E), as well as granulocyte/macrophage (GM-CFU) and megakaryocytic (CFU-Meg) lineages. It is concluded that the persistent erythropoietic stress results in a selective expansion of immature hemopoietic cells and inappropriate production of nonerythroid blood cells from excess production of progenitor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow / pathology
  • Bone Marrow / physiology
  • Female
  • Granulocytes / pathology
  • Granulocytes / physiology
  • Hematopoiesis / physiology*
  • Hematopoietic Stem Cells / pathology
  • Hematopoietic Stem Cells / physiology
  • Macrophages / pathology
  • Macrophages / physiology
  • Male
  • Megakaryocytes / pathology
  • Megakaryocytes / physiology
  • Mice
  • Mice, Inbred C57BL
  • Spleen / pathology
  • Spleen / physiopathology*
  • beta-Thalassemia / pathology
  • beta-Thalassemia / physiopathology*