TAp63 regulates VLA-4 expression and chronic lymphocytic leukemia cell migration to the bone marrow in a CD74-dependent manner

J Immunol. 2010 May 1;184(9):4761-9. doi: 10.4049/jimmunol.0904149. Epub 2010 Mar 31.

Abstract

The hallmark of chronic lymphocytic leukemia (CLL) is the relentless accumulation of mature lymphocytes, mostly due to their decreased apoptosis. CD74 was recently shown to serve as a survival receptor on CLL cells. In this study, we show that stimulation of CD74 with its natural ligand, migration inhibitory factor, initiates a signaling cascade that results in upregulation of TAp63, which directly regulates CLL survival. In addition, TAp63 expression elevates the expression of the integrin VLA-4, particularly during the advanced stage of the disease. Blocking of CD74, TAp63, or VLA-4 inhibits the in vivo homing of CLL cells to the bone marrow (BM). Thus, CD74 and its target genes TAp63 and VLA-4 facilitate migration of CLL cells back to the BM, where they interact with the supportive BM environment that rescues them from apoptosis. These results could form the basis of novel therapeutic strategies aimed at blocking homing of CLL cells in their return to the BM and attenuating their survival.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antibodies, Blocking / pharmacology
  • Antigens, Differentiation, B-Lymphocyte / immunology
  • Antigens, Differentiation, B-Lymphocyte / metabolism
  • Antigens, Differentiation, B-Lymphocyte / physiology*
  • Antigens, Neoplasm / biosynthesis
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / physiology
  • Apoptosis Regulatory Proteins / biosynthesis
  • Apoptosis Regulatory Proteins / genetics
  • Apoptosis Regulatory Proteins / physiology
  • Bone Marrow Cells / immunology*
  • Bone Marrow Cells / pathology*
  • Cell Migration Inhibition / immunology
  • Cell Movement / genetics
  • Cell Movement / immunology
  • Cell Survival / genetics
  • Cell Survival / immunology
  • Female
  • Gene Expression Regulation, Neoplastic / immunology*
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Antigens Class II / metabolism
  • Histocompatibility Antigens Class II / physiology*
  • Humans
  • Integrin alpha4beta1 / biosynthesis
  • Integrin alpha4beta1 / genetics*
  • Intramolecular Oxidoreductases / antagonists & inhibitors
  • Intramolecular Oxidoreductases / physiology
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology*
  • Macrophage Migration-Inhibitory Factors / antagonists & inhibitors
  • Macrophage Migration-Inhibitory Factors / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Signal Transduction / immunology
  • Trans-Activators / biosynthesis
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transcription Factors
  • Tumor Suppressor Proteins / biosynthesis
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / physiology*
  • Up-Regulation / immunology

Substances

  • Antibodies, Blocking
  • Antigens, Differentiation, B-Lymphocyte
  • Antigens, Neoplasm
  • Apoptosis Regulatory Proteins
  • Histocompatibility Antigens Class II
  • Integrin alpha4beta1
  • Macrophage Migration-Inhibitory Factors
  • TP63 protein, human
  • Trans-Activators
  • Transcription Factors
  • Tumor Suppressor Proteins
  • invariant chain
  • Intramolecular Oxidoreductases
  • MIF protein, human