Essential role for ALCAM gene silencing in megakaryocytic differentiation of K562 cells

BMC Mol Biol. 2010 Dec 2:11:91. doi: 10.1186/1471-2199-11-91.

Abstract

Background: Activated leukocyte cell adhesion molecule (ALCAM/CD166) is expressed by hematopoietic stem cells. However, its role in hematopoietic differentiation has not previously been defined.

Results: In this study, we show that ALCAM expression is silenced in erythromegakaryocytic progenitor cell lines. In agreement with this finding, the ALCAM promoter is occupied by GATA-1 in vivo, and a cognate motif at -850 inhibited promoter activity in K562 and MEG-01 cells. Gain-of-function studies showed that ALCAM clusters K562 cells in a process that requires PKC. Induction of megakaryocytic differentiation in K562 clones expressing ALCAM activated PKC-δ and triggered apoptosis.

Conclusions: There is a lineage-specific silencing of ALCAM in bi-potential erythromegakaryocytic progenitor cell lines. Marked apoptosis of ALCAM-expressing K562 clones treated with PMA suggests that aberrant ALCAM expression in erythromegakaryocytic progenitors may contribute to megakaryocytopenia.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Activated-Leukocyte Cell Adhesion Molecule / genetics*
  • Apoptosis
  • Cell Lineage
  • GATA1 Transcription Factor / metabolism
  • Gene Expression Regulation
  • Gene Silencing*
  • Hematopoiesis*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • K562 Cells
  • Megakaryocytes / cytology*
  • Megakaryocytes / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Kinase C / metabolism

Substances

  • Activated-Leukocyte Cell Adhesion Molecule
  • GATA1 Transcription Factor
  • Protein Kinase C