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Promotion of megakaryocyte progenitor expansion and differentiation by the c-Mpl ligand thrombopoietin

  • Kenneth Kaushansky*
  • , Si Lok
  • , Richard D. Holly
  • , Virginia C. Broudy
  • , Nancy Lin
  • , Mason C. Bailey
  • , John W. Forstrom
  • , Michele M. Buddle
  • , Pieter J. Oort
  • , Fredrick S. Hagen
  • , Gerald J. Roth
  • , Thalia Papayannopoulou
  • , Donald C. Foster
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

987 Scopus citations

Abstract

THE development of blood cells including expansion of megakaryocyte progenitor cells requires the interplay of marrow stromal cells and polypeptide cytokines1-10. Recently, characterization of c-Mpl, the receptor encoded by the proto-oncogene c-mpl, revealed structural homology with the haematopoietic cytokine receptor family11, and its involvement in megakaryocyte development12 We report here that the ligand for c-Mpl13 is relatively lineage specific, works both alone and synergistically with early acting cytokines to support megakaryocyte colony formation, and acts at a late stage of development to increase megakaryocyte size, polyploidization and expression of differentiation markers. In vivo, c-Mpl ligand stimulates platelet production by greatly expanding marrow and splenic megakaryocytes and their progenitors, and by shifting the distribution of megakaryocyte ploidy to higher values. Thus, as c-Mpl ligand has the expected characteristics of the major regulator of megakaryocyte development, we propose that it be termed thrombopoietin.

Original languageEnglish
Pages (from-to)568-571
Number of pages4
JournalNature
Volume369
Issue number6481
DOIs
StatePublished - 1994
Externally publishedYes

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