The AML1/ETO target gene LAT2 interferes with differentiation of normal hematopoietic precursor cells

Leuk Res. 2014 Mar;38(3):340-5. doi: 10.1016/j.leukres.2013.12.014. Epub 2013 Dec 25.

Abstract

The adaptor protein linker activator of T-cells 2 (LAT2) is a known AML1/ETO target gene whose function during normal hematopoiesis is unknown. We addressed the role of LAT2 during erythroid and myeloid differentiation of normal human CD34+ hematopoietic cells. LAT2 is expressed at low levels in CD34+ cells and upregulated during cytokine-induced myeloid and erythroid differentiation. Forced LAT2 expression leads to a delay of erythroid and myeloid differentiation keeping CD34+ cells in a more immature state, whereas LAT2 knockdown accelerates differentiation. It is tempting to speculate that by affecting the differentiation capacity of normal hematopoietic progenitors, LAT2 may contribute to the pathogenesis of AML.

Keywords: Acute myeloid leukemia; Adaptor molecule; Erythroid differentiation; Myeloid differentiation.

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / antagonists & inhibitors
  • Adaptor Proteins, Signal Transducing / genetics*
  • Adaptor Proteins, Signal Transducing / immunology
  • Antigens, CD34 / genetics
  • Antigens, CD34 / immunology
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Core Binding Factor Alpha 2 Subunit / genetics*
  • Core Binding Factor Alpha 2 Subunit / immunology
  • Gene Expression Regulation
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • Granulocytes / cytology
  • Granulocytes / drug effects
  • Granulocytes / immunology
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects*
  • Hematopoietic Stem Cells / immunology
  • Humans
  • Interleukin-3 / pharmacology
  • Leukocytes, Mononuclear
  • Lymphocyte Activation
  • Lymphocytes / cytology
  • Lymphocytes / drug effects
  • Lymphocytes / immunology
  • Monocytes / cytology
  • Monocytes / drug effects
  • Monocytes / immunology
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins / immunology
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • RUNX1 Translocation Partner 1 Protein
  • Signal Transduction
  • Stem Cell Factor / pharmacology
  • Transcription Factors / genetics*
  • Transcription Factors / immunology

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, CD34
  • Core Binding Factor Alpha 2 Subunit
  • Interleukin-3
  • LAT2 protein, human
  • Proto-Oncogene Proteins
  • RNA, Small Interfering
  • RUNX1 Translocation Partner 1 Protein
  • RUNX1 protein, human
  • RUNX1T1 protein, human
  • Stem Cell Factor
  • Transcription Factors
  • Granulocyte-Macrophage Colony-Stimulating Factor