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 language | English |
|---|---|
| Pages (from-to) | 568-571 |
| Number of pages | 4 |
| Journal | Nature |
| Volume | 369 |
| Issue number | 6481 |
| DOIs | |
| State | Published - 1994 |
| Externally published | Yes |