Cloning and expression of murine thrombopoietin cDNA and stimulation of platelet production in vivo

Si Lok, Kenneth Kaushansky, Richard D. Holly, Joseph L. Kuijper, Catherine E. Lofton-Day, Pieter J. Oort, Francis J. Grant, Mark D. Heipel, Steve K. Burkhead, Janet M. Kramer, L. Anne Bell, Cindy A. Sprecher, Hal Blumberg, Rebecca Johnson, Donna Prunkard, Andrew F.T. Ching, Shannon L. Mathewes, Mason C. Bailey, John W. Forstrom, Michele M. BuddleSherri G. Osborn, Simon J. Evans, Paul O. Sheppard, Scott R. Presnell, Patrick J. O'Hara, Fredrick S. Hagen, Gerald J. Roth, Donald C. Foster*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

1089 Scopus citations

Abstract

THE major regulator of circulating platelet levels is believed to be a cytokine termed thrombopoietin1,2. It is thought to be a lineage-specific cytokine affecting the proliferation and maturation of committed cells resulting in the production of megakaryocytes and platelets. Despite considerable efforts by a number of laboratories, the unequivocal identification of thrombopoietin has proven elusive. Here we report the functional cloning of a murine complementary DNA encoding a ligand for the receptor encoded by the c-mpl proto-oncogene (c-Mpl) 3-5. The encoded polypeptide has a predicted molecular mass of 35,000 (Mr 35K). The protein has a novel two-domain structure with an amino-terminal domain homologous with erythropoietin and a carboxy-terminal domain rich in serine, threonine and proline residues and containing seven potential N-linked glycosylation sites. Intraperitoneal injections of mice with recombinant protein increase circulating platelet levels by greater than fourfold after 7 days. These results along with those presented in the accompanying report strongly suggest that the ligand for c-Mpl is thrombopoietin.

Original languageEnglish
Pages (from-to)565-568
Number of pages4
JournalNature
Volume369
Issue number6481
DOIs
StatePublished - 1994
Externally publishedYes

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