Notch-3 and Notch-4 signaling rescue from apoptosis human B-ALL cells in contact with human bone marrow-derived mesenchymal stromal cells

Blood. 2011 Jul 14;118(2):380-9. doi: 10.1182/blood-2010-12-326694. Epub 2011 May 20.

Abstract

Although many literature data are available on the role of Notch signaling in T-cell acute lymphoblastic leukemia (ALL) biology, the importance of this molecular pathway in the development of B-lineage ALL (B-ALL) cells in the BM microenvironment is unknown so far. In this study, we used anti-Notch molecules neutralizing Abs and γ-secretase inhibitor (GSI) XII to investigate the role of the Notch signaling pathway in the promotion of human B-ALL cell survival in presence of stromal cell support. The treatment with combinations of anti-Notch molecule neutralizing Abs resulted in the decrease of B-ALL cell survival, either cultured alone or cocultured in presence of stromal cells from normal donors and B-ALL patients. Interestingly, the inhibition of Notch-3 and -4 or Jagged-1/-2 and DLL-1 resulted in a dramatic increase of apoptotic B-ALL cells by 3 days, similar to what is obtained by blocking all Notch signaling with the GSI XII. Our data suggest that the stromal cell-mediated antiapoptotic effect on B- ALL cells is mediated by Notch-3 and -4 or Jagged-1/-2 and DLL-1 in a synergistic manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / genetics*
  • B-Lymphocytes / pathology
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / physiology*
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / metabolism
  • Calcium-Binding Proteins / physiology
  • Cell Communication / genetics
  • Cell Communication / physiology
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Intercellular Signaling Peptides and Proteins / physiology
  • Jagged-1 Protein
  • Jagged-2 Protein
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Membrane Proteins / physiology
  • Mesenchymal Stem Cells / metabolism
  • Mesenchymal Stem Cells / physiology
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / physiology*
  • Receptor, Notch3
  • Receptor, Notch4
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism
  • Receptors, Notch / physiology*
  • Serrate-Jagged Proteins
  • Signal Transduction / genetics
  • Signal Transduction / physiology
  • Stromal Cells / metabolism
  • Stromal Cells / physiology*
  • Tumor Cells, Cultured

Substances

  • Calcium-Binding Proteins
  • DLK1 protein, human
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • JAG2 protein, human
  • Jagged-1 Protein
  • Jagged-2 Protein
  • Membrane Proteins
  • NOTCH3 protein, human
  • NOTCH4 protein, human
  • Proto-Oncogene Proteins
  • Receptor, Notch3
  • Receptor, Notch4
  • Receptors, Notch
  • Serrate-Jagged Proteins