Myeloid or lymphoid promiscuity as a critical step in hematopoietic lineage commitment

Dev Cell. 2002 Jul;3(1):137-47. doi: 10.1016/s1534-5807(02)00201-0.

Abstract

We demonstrate here that "promiscuous" expression of myeloid or lymphoid genes precedes lineage commitment in hematopoiesis. Prospectively purified single common myeloid progenitors (CMPs) coexpress myelo-erythroid but not lymphoid genes, whereas single common lymphoid progenitors (CLPs) coexpress T and B lymphoid but not myeloid genes. Genes unrelated to the adopted lineage are downregulated in bipotent and monopotent descendants of CMPs and CLPs. Promiscuous gene expression does not alter the biological potential of multipotent progenitors: CMPs with an activated endogenous M lysozyme locus yield normal proportions of myelo-erythroid colonies, and CLPs expressing the pre-T cell receptor alpha gene differentiate into normal numbers of B cells. Thus, the accessibility for multiple myeloid or lymphoid programs promiscuously may allow flexibility in fate commitments at these multipotent stages.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / metabolism
  • Bone Marrow / embryology*
  • Bone Marrow / metabolism
  • Cell Differentiation / genetics*
  • Cell Lineage / genetics*
  • Cells, Cultured
  • Erythrocytes / cytology
  • Erythrocytes / metabolism
  • Female
  • Gene Expression Regulation, Developmental / physiology
  • Genotype
  • Hematopoiesis / genetics*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • Lymphocytes / cytology
  • Lymphocytes / metabolism*
  • Male
  • Megakaryocytes / cytology
  • Megakaryocytes / metabolism
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Mutant Strains
  • Muramidase / genetics
  • Muramidase / metabolism
  • Myeloid Cells / cytology
  • Myeloid Cells / metabolism*
  • Proteins / genetics
  • Proteins / metabolism
  • Receptors, Antigen, T-Cell, alpha-beta
  • T-Lymphocytes / cytology
  • T-Lymphocytes / metabolism
  • Transcriptional Activation / physiology

Substances

  • Membrane Glycoproteins
  • Proteins
  • Receptors, Antigen, T-Cell, alpha-beta
  • pre-T cell receptor alpha
  • Muramidase