Disparate effects of interleukin 11 and thrombopoietin on megakaryocytopoiesis in vitro

Cytokine. 2001 Sep 7;15(5):241-9. doi: 10.1006/cyto.2001.0928.

Abstract

The effects of interleukin-11 (IL-11) and thrombopoietin (TPO) on murine megakaryocytopoiesis were studied using a serum-free culture system. Acting alone, both IL-11 and TPO increased the number of acetylcholinesterase (AchE)(+)cells (megakaryocytes), the latter being more potent than the former. TPO, but not IL-11, increased the mean AchE activity per megakaryocyte (AchE activity/megakaryocyte). TPO increased both the number of megakaryocytes with high ploidy, and of those with low ploidy. In contrast, IL-11 increased only the number of megakaryocytes with high ploidy. The effect of TPO on megakaryocyte ploidy was stronger than that of IL-11. Both IL-11 and TPO increased the proportion of large megakaryocytes, but the latter was more potent than the former. While the stimulatory effects of IL-11 and TPO on the number of megakaryocytes were enhanced by IL-3 or stem cell factor (SCF), synergism of IL-11 or TPO with IL-3 or SCF in stimulating AchE activity/megakaryocyte was inconsistent. IL-11 and TPO stimulated the formation of colony-forming units of megakaryocyte in the presence of IL-3, but not alone, with similar maximum colony numbers for both cytokines. Our findings thus demonstrate that IL-11 principally stimulates megakaryocyte maturation rather than the proliferation of megakaryocytes, whereas TPO stimulates both.

MeSH terms

  • Acetylcholinesterase / biosynthesis
  • Animals
  • Bone Marrow Cells / cytology
  • Cell Division
  • Cell Line
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Culture Media, Serum-Free / pharmacology
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • In Vitro Techniques
  • Interleukin-11 / pharmacology*
  • Interleukin-11 / physiology*
  • Interleukin-3 / biosynthesis
  • Megakaryocytes / cytology
  • Megakaryocytes / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Ploidies
  • Recombinant Proteins / metabolism
  • Stem Cell Factor / biosynthesis
  • Thrombopoietin / pharmacology*
  • Thrombopoietin / physiology*

Substances

  • Culture Media, Serum-Free
  • Interleukin-11
  • Interleukin-3
  • Recombinant Proteins
  • Stem Cell Factor
  • DNA
  • Thrombopoietin
  • Acetylcholinesterase