Bone and bone marrow interactions: hematological activity of osteoblastic growth peptide (OGP)-derived carboxy-terminal pentapeptide:
III. Action on human megakaryocytopoiesis: focus on essential thrombocythemia
Abstract
The increase of megakaryocytes and platelets that characterizes essential thrombocythemia (ET) appears to be secondary to a deregulation of megakaryocytopoiesis. The carboxy-terminal fragment of osteogenic growth peptide (OGP10–14) promotes bone formation and hemopoiesis, while it inhibits megakaryocytopoiesis. In this paper we show that treatment with synthetic OGP10–14 (sOGP10–14) induces a significant reduction of mid and large colony-forming unit-megakaryocytes (CFU-Mk) in ET patients as well as in controls, and is associated with a significant inhibition of thrombopoietin (TPO)-primed MO-7e megakaryoblastic cells proliferation. These actions appear to be related to sOGP10–14 modulation of TGF-β1 synthesis and/or secretion, although a direct effect on TGF-β receptor expression cannot be excluded.
Keywords: OGP10–14, Megakaryocytopoiesis, Essential thrombocythemia, TGF-β1, CFU-Mk
To access this article, please choose from the options below
PII: S0145-2126(04)00064-5
doi:10.1016/j.leukres.2004.01.019
© 2004 Elsevier Ltd. All rights reserved.
