STAT3 controls myeloid progenitor growth during emergency granulopoiesis

Blood. 2010 Oct 7;116(14):2462-71. doi: 10.1182/blood-2009-12-259630. Epub 2010 Jun 25.

Abstract

Granulocyte colony-stimulating factor (G-CSF) mediates "emergency" granulopoiesis during infection, a process that is mimicked by clinical G-CSF use, yet we understand little about the intracellular signaling cascades that control demand-driven neutrophil production. Using a murine model with conditional deletion of signal transducer and activator of transcription 3 (STAT3) in bone marrow, we investigated the cellular and molecular mechanisms of STAT3 function in the emergency granulopoiesis response to G-CSF administration or infection with Listeria monocytogenes, a pathogen that is restrained by G-CSF signaling in vivo. Our results show that STAT3 deficiency renders hematopoietic progenitor cells and myeloid precursors refractory to the growth-promoting functions of G-CSF or L monocytogenes infection. STAT3 is necessary for accelerating granulocyte cell-cycle progression and maturation in response to G-CSF. STAT3 directly controls G-CSF-dependent expression of CCAAT-enhancer-binding protein β (C/EBPβ), a crucial factor in the emergency granulopoiesis response. Moreover, STAT3 and C/EBPβ coregulate c-Myc through interactions with the c-myc promoter that control the duration of C/EBPα occupancy during demand-driven granulopoiesis. These results place STAT3 as an essential mediator of emergency granulopoiesis by its regulation of transcription factors that direct G-CSF-responsive myeloid progenitor expansion.

Publication types

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

MeSH terms

  • Animals
  • CCAAT-Enhancer-Binding Protein-beta / genetics
  • CCAAT-Enhancer-Binding Proteins / genetics
  • Cell Cycle
  • Gene Expression Regulation
  • Granulocyte Colony-Stimulating Factor / metabolism*
  • Granulocytes / cytology*
  • Granulocytes / metabolism
  • Granulocytes / microbiology
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / metabolism
  • Hematopoietic Stem Cells / microbiology
  • Leukopoiesis*
  • Listeria monocytogenes / pathogenicity
  • Mice
  • Promoter Regions, Genetic
  • Proto-Oncogene Proteins c-myc / genetics
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, mouse
  • Cebpb protein, mouse
  • Proto-Oncogene Proteins c-myc
  • STAT3 Transcription Factor
  • Granulocyte Colony-Stimulating Factor