GABP is necessary for stem/progenitor cell maintenance and myeloid differentiation in human hematopoiesis and chronic myeloid leukemia

Stem Cell Res. 2016 May;16(3):677-81. doi: 10.1016/j.scr.2016.04.007. Epub 2016 Apr 12.

Abstract

Maintenance of hematopoietic stem cells and their potential to give rise to progenitors of differentiated lymphoid and myeloid cells are accomplished by a network of regulatory processes. As a part of this network, the heteromeric transcription factor GA-binding protein (GABP) plays a crucial role in self-renewal of murine hematopoietic and leukemic stem cells. Here, we report the consequences of functional impairment of GABP in human hematopoietic and in leukemic stem/progenitor cells. Ectopic overexpression of a dominant-negative acting GABP mutant led to impaired myeloid differentiation of CD34(+) hematopoietic stem/progenitor cells obtained from healthy donors. Moreover, drastically reduced clonogenic capacity of leukemic stem/progenitor cells isolated from bone marrow aspirates of chronic myeloid leukemia (CML) patients underlines the importance of GABP on stem/progenitor cell maintenance and confirms the relevance of GABP for human myelopoiesis in healthy and diseased states.

Keywords: CML/chronic myeloid leukemia; GABP; Hematopoietic stem cell; Leukemic stem cell; Transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged, 80 and over
  • Antigens, CD34 / metabolism
  • Bone Marrow Cells / cytology
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • GA-Binding Protein Transcription Factor / antagonists & inhibitors
  • GA-Binding Protein Transcription Factor / genetics
  • GA-Binding Protein Transcription Factor / metabolism*
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Imatinib Mesylate / toxicity
  • K562 Cells
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology*
  • Male
  • Mutation
  • Myeloid Cells / cytology*
  • Myeloid Cells / metabolism
  • Myelopoiesis
  • RNA Interference
  • RNA, Small Interfering / metabolism

Substances

  • Antigens, CD34
  • GA-Binding Protein Transcription Factor
  • RNA, Small Interfering
  • Imatinib Mesylate