Interaction of AP-1 and the ctgf gene: a possible driver of chondrocyte hypertrophy in growth cartilage

J Bone Miner Metab. 2003;21(4):205-10. doi: 10.1007/s00774-003-0410-1.

Abstract

The expression of the connective tissue growth factor ( ctgf) gene increases along with the differentiation of growth cartilage cells, and the highest expression is observed in the hypertrophic stage. Similarly, recent reports demonstrated c- fos expression in chondrocytes in the early hypertrophic zone of growth cartilage, and suggested that the c- fos gene may play a crucial role in the regulation of hypertrophic differentiation. A chondrocytic human cell line, HCS-2/8, is known to retain a variety of chondrocytic phenotypes. When such cells were kept overconfluent, they expressed increasing levels of c- fos transcripts along a time course phenotypically similar to that of hypertrophic differentiation. Moreover, by using a competitive electromobility-shift assay, we found that AP-1, a Fos/Jun heterodimer, in HCS-2/8 was capable of binding not only to a typical AP-1-binding DNA fragment but also to the enhancer fragment of the ctgf gene. Based on the findings above, we hypothesize that, prior to hypertrophic differentiation, AP-1-related oncogenes are activated and that their gene products subsequently activate ctgf gene expression, which might eventually induce hypertrophy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Cartilage / growth & development*
  • Cartilage / pathology*
  • Cell Division / genetics
  • Cells, Cultured
  • Chondrocytes / pathology*
  • Connective Tissue Growth Factor
  • Enhancer Elements, Genetic
  • Gene Expression Regulation
  • Genes, fos / genetics
  • Growth Plate / cytology
  • Growth Plate / metabolism
  • Humans
  • Hypertrophy / genetics
  • Hypertrophy / pathology
  • Immediate-Early Proteins / genetics*
  • Immediate-Early Proteins / metabolism
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Proto-Oncogenes / genetics
  • Transcription Factor AP-1 / genetics*
  • Transcription Factor AP-1 / metabolism

Substances

  • CCN2 protein, human
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • Transcription Factor AP-1
  • Connective Tissue Growth Factor