Chemokine stromal cell-derived factor-1 induction by C/EBPbeta activation is associated with all-trans-retinoic acid-induced leukemic cell differentiation

J Leukoc Biol. 2007 Nov;82(5):1332-9. doi: 10.1189/jlb.1106697. Epub 2007 Jul 26.

Abstract

Stromal cell-derived factor-1 (SDF-1/CXCL12) is one of the essential chemokines, which mediates hematopoietic differentiations. However, the mechanism by which SDF-1 expression is regulated in granulocyte differentiation is poorly understood. Here, we suggest a novel mechanism by which all-trans-retinoic acid (ATRA) induces the expression of SDF-1 during the differentiation of promyelomonocytic leukemic U937 cells. Moreover, we also demonstrate that activation of transcription factor C/EBPbeta by ATRA regulates SDF-1 expression in U937 cells. In addition, we show that the cyclin-dependent kinase inhibitors p21(WAF1/CIP1) and Pyk2 are up-regulated by SDF-1 and increased markedly by the costimulation of ATRA and SDF-1. Furthermore, ATRA and SDF-1alpha additively induce U937 cell differentiation. Indeed, silencing the expression of SDF-1 inhibits ATRA-induced granulocyte differentiation significantly. Taken together, these results indicate that SDF-1alpha is involved in granulocyte differentiation in response to ATRA, mediated by the activation of the transcription factor C/EBPbeta.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Blotting, Western
  • CCAAT-Enhancer-Binding Protein-beta / metabolism*
  • Cell Differentiation / drug effects*
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / metabolism*
  • Chemokines / pharmacology
  • Chromatin Immunoprecipitation
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Gene Expression Regulation, Leukemic / drug effects*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Granulocytes / drug effects
  • Granulocytes / metabolism
  • Humans
  • Luciferases / metabolism
  • Promoter Regions, Genetic
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • RNA, Small Interfering / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transfection
  • Tretinoin / pharmacology*
  • U937 Cells / drug effects
  • U937 Cells / metabolism

Substances

  • Antineoplastic Agents
  • CCAAT-Enhancer-Binding Protein-beta
  • CXCL12 protein, human
  • Chemokine CXCL12
  • Chemokines
  • Cyclin-Dependent Kinase Inhibitor p21
  • RNA, Neoplasm
  • RNA, Small Interfering
  • Tretinoin
  • Luciferases