Altered natural killer cell differentiation in CD34+ progenitors from chronic myeloid leukemia patients

Oncogene. 2000 May 25;19(23):2758-66. doi: 10.1038/sj.onc.1203584.

Abstract

IL-15 and SCF fail to induce NK differentiation and proliferation of CD34+ hematopoietic progenitors from chronic myeloid leukemia patients in contrast to normal stem cells although, both normal and leukemic CD34+ cells display comparable expression of c-kit or IL-15 receptor subunits. Interestingly, confocal microscopy analysis revealed that leukemic and most normal CD34+ cells produce and secrete IL-15, as shown by its trafficking through the Golgi apparatus and early endosomes. However, only leukemic progenitors express the membrane bound IL-15. Colocalization and internalization of IL-15Rbeta/gammac and IL-15Ralpha/gammac complexes indicated that IL-15 was specifically uptaken by leukemic progenitors. We also demonstrated that in both normal and leukemic progenitors, the signaling kinase Jak3 is constitutively pre-associated with the gammac chain. Anti-IL-15 neutralizing mAb treatment resulted in down-regulation of gammac chain and disruption of gammac/Jak3 interaction in normal but had no effect in leukemic progenitors. Our results suggest the existence in both normal and leukemic CD34+ cells of a constitutive production of a bioactive IL-15 that does not lead to NK differentiation and further indicate that membrane bound IL-15 and constitutive activation of gammac are hallmarks of leukemic progenitors. Oncogene (2000).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD34 / metabolism*
  • Cell Differentiation
  • Cell Division
  • Cell Line
  • Humans
  • Interleukin-15 / metabolism
  • Interleukin-15 / pharmacology
  • Killer Cells, Natural / pathology*
  • Killer Cells, Natural / physiology
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology*
  • Lymphocyte Subsets / pathology*
  • Lymphocyte Subsets / physiology
  • Microscopy, Confocal
  • Receptors, Interleukin-15
  • Receptors, Interleukin-2 / metabolism
  • Stem Cell Factor / metabolism
  • Stem Cell Factor / pharmacology
  • Tumor Cells, Cultured

Substances

  • Antigens, CD34
  • IL15RA protein, human
  • Interleukin-15
  • Receptors, Interleukin-15
  • Receptors, Interleukin-2
  • Stem Cell Factor