Microenvironmentally dependent effects on murine haemopoiesis by a prolonged interleukin-1 treatment

Br J Haematol. 1993 Sep;85(1):15-9. doi: 10.1111/j.1365-2141.1993.tb08639.x.

Abstract

We administered recombinant human IL-1 beta (400 ng/d, s.c.) for 10 d to normal C57B1 mice and determined daily granuloid and erythroid parameters in marrow, spleen and blood. In the marrow CFU-GM numbers were not affected but later granuloid cell stages were moderately enhanced (170%). In the spleen, however, CFU-GM numbers were sharply increased (1600%), whereas the granuloid precursors only doubled. Blood granulocytes increased transiently to 275% on day 5. In the marrow all erythroid parameters were severely reduced. This reduction was partially compensated by the spleen where initially only BFU-E and with some delay also more mature erythroid cells accumulated. At the end of the treatment mice were slightly anaemic. When mice were treated with IL-1 and erythropoietin (10 U/d) simultaneously, the inhibitory effects on erythropoiesis were less severe. In agreement with in vivo results, IL-1 inhibited in vitro colony growth of CFU-E from normal bone marrow and spleen but spleen CFU-E from 5 d IL-1 treated mice were insensitive. We conclude that IL-1 can induce stimulation or inhibition of haemopoietic progenitor cells depending on their microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells
  • Cells, Cultured
  • Colony-Forming Units Assay
  • Drug Administration Schedule
  • Erythroid Precursor Cells / drug effects
  • Erythropoiesis / drug effects
  • Erythropoietin / pharmacology
  • Female
  • Granulocytes / cytology
  • Granulocytes / drug effects
  • Hematopoiesis / drug effects*
  • Interleukin-1 / pharmacology*
  • Mice
  • Mice, Inbred C57BL
  • Recombinant Proteins / pharmacology
  • Spleen / cytology

Substances

  • Interleukin-1
  • Recombinant Proteins
  • Erythropoietin