Balance between Id and E proteins regulates myeloid-versus-lymphoid lineage decisions

• DOI: 10.1182/blood-2008-06-164996
• Publication Date: 2008-10-17T01:36:56Z
• Authors: Shawn W. Cochrane; Ying Zhao; Robert S. Welner; Xiao-Hong Sun
• Keywords: Inhibitor of Differentiation Protein 1; Myelopoiesis; 0301 basic medicine; B-Lymphocytes; Lymphopoiesis; Multipotent Stem Cells; Transcription Factor 7-Like 1 Protein; Cell Differentiation; Mice, Transgenic; Mice; 03 medical and health sciences; Granulocyte-Macrophage Progenitor Cells; Animals; TCF Transcription Factors

Abstract Hematopoiesis consists of a series of lineage decisions controlled by specific gene expression that is regulated by transcription factors and intracellular signaling events in response to environmental cues. Here, we demonstrate that the balance between E-protein transcription factors and their inhibitors, Id proteins, is important for the myeloid-versus-lymphoid fate choice. Using Id1-GFP knockin mice, we show that transcription of the Id1 gene begins to be up-regulated at the granulocyte-macrophage progenitor stage and continues throughout myelopoiesis. Id1 expression is also stimulated by cytokines favoring myeloid differentiation. Forced expression of Id1 in multipotent progenitors promotes myeloid development and suppresses B-cell formation. Conversely, enhancing E-protein activity by expressing a variant of E47 resistant to Id-mediated inhibition prevents the myeloid cell fate while driving B-cell differentiation from lymphoid-primed multipotent progenitors. Together, these results suggest a crucial function for E proteins in the myeloid-versus-lymphoid lineage decision.