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Background: Transcription factors are essential for blood cell formation. Mice expressing low levels of c-Myb (c-Myb low ) have an increased number of bone marrow megakaryocytes (MKs) and corresponding thrombocytosis. In contrast, mice engineered to express low levels of GATA-1 (GATA-1 low ) in the megakaryocytic lineage exhibit aberrant megakaryocytopoiesis with hyperproliferation of progenitors and defective terminal differentiation leading to thrombocytopenia. These seemingly opposite roles may affect platelet turnover and thus be of clinical relevance. Objective: To determine how these two transcription factors act together to control megakaryocytopoiesis and platelet formation. Methods: We used a combination of cellular and molecular in vitro assays to examine the ability of bone marrow cells from mice expressing low levels of both c-Myb and GATA-1 (referred to as double low ) to produce MKs and platelets. Results: Double low cells, or those with low GATA-1 levels in which c-Myb is conditionally deleted, lack the hyperproliferative capacity of GATA-1 low cells, allowing the cells to proceed towards more committed MKs that are, however, impaired in their capacity to produce fully differentiated cells, as confirmed by the abundance of morphologically aberrant cells that lack the ability to form proplatelets. Conclusion: c-Myb and GATA-1 act in concert to achieve correct megakaryocytic differentiation. GATA-1 regulates both the proliferation of megakaryocytic progenitors and their terminal maturation. c-Myb also acts at the level of the progenitor by influencing its commitment to differentiation, but in contrast to GATA-1 it does not have any effect on the process of terminal differentiation. © 2011 International Society on Thrombosis and Haemostasis.

Original publication

DOI

10.1111/j.1538-7836.2011.04396.x

Type

Journal article

Journal

Journal of Thrombosis and Haemostasis

Publication Date

01/08/2011

Volume

9

Pages

1572 - 1581