A critical role for the transcription factor Scl in platelet production during stress thrombopoiesis

Blood. 2006 Oct 1;108(7):2248-56. doi: 10.1182/blood-2006-02-002188. Epub 2006 Jun 8.

Abstract

The generation of platelets from megakaryocytes in the steady state is regulated by a variety of cytokines and transcription factors, including thrombopoietin (TPO), GATA-1, and NF-E2. Less is known about platelet production in the setting of stress thrombopoiesis, a pivotal event in the context of cytotoxic chemotherapy. Here we show in mice that the transcription factor Scl is critical for platelet production after chemotherapy and in thrombopoiesis induced by administration of TPO. Megakaryocytes from these mice showed appropriate increases in number and ploidy but failed to shed platelets. Ultrastructural examination of Scl-null megakaryocytes revealed a disorganized demarcation membrane and reduction in platelet granules. Quantitative real-time polymerase chain reaction showed that Scl-null platelets lacked NF-E2, and chromatin immunoprecipitation analysis demonstrated Scl binding to the NF-E2 promoter in the human megakaryoblastic-cell line Meg-01, along with its binding partners E47, Lmo2, and the cofactors Ldb1 and GATA-2. These findings suggest that Scl acts up-stream of NF-E2 expression to control megakaryocyte development and platelet release in settings of thrombopoietic stress.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / physiology*
  • Blood Platelets / metabolism*
  • Blood Platelets / physiology
  • Chromatin Immunoprecipitation
  • Humans
  • Megakaryocytes / cytology
  • Megakaryocytes / ultrastructure
  • Mice
  • NF-E2 Transcription Factor, p45 Subunit / metabolism
  • Platelet Aggregation
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / physiology*
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Thrombocytosis
  • Thrombopoiesis / physiology*
  • Thrombopoietin / metabolism

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • NF-E2 Transcription Factor, p45 Subunit
  • Nfe2 protein, mouse
  • Proto-Oncogene Proteins
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Tal1 protein, mouse
  • Thrombopoietin