Human immortalized chondrocytes carrying heterozygous FGFR3 mutations: an in vitro model to study chondrodysplasias

FEBS Lett. 2007 Jun 12;581(14):2593-8. doi: 10.1016/j.febslet.2007.04.079. Epub 2007 May 8.

Abstract

Achondroplasia and thanatophoric dysplasia are human chondrodysplasias caused by mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. We have developed an immortalized human chondrocyte culture model to study the regulation of chondrocyte functions. One control and eight mutant chondrocytic lines expressing different FGFR3 heterozygous mutations were obtained. FGFR3 signaling pathways were modified in the mutant lines as revealed by the constitutive activation of the STAT pathway and an increased level of P21(WAF1/CIP1) protein. This model will be useful for the study of FGFR3 function in cartilage studies and future therapeutic approaches in chondrodysplasias.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cell Line, Transformed
  • Cells, Cultured
  • Chondrocytes / cytology
  • Chondrocytes / metabolism*
  • Collagen Type II / genetics
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Gene Expression
  • Heterozygote
  • High Mobility Group Proteins / genetics
  • Humans
  • Immunoblotting
  • Microscopy, Fluorescence
  • Mitogen-Activated Protein Kinases / metabolism
  • Mutation*
  • Osteochondrodysplasias / genetics
  • Osteochondrodysplasias / pathology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics*
  • Receptor, Fibroblast Growth Factor, Type 3 / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • SOX9 Transcription Factor
  • STAT Transcription Factors / metabolism
  • Signal Transduction / genetics
  • Signal Transduction / physiology
  • Transcription Factors / genetics

Substances

  • CDKN1A protein, human
  • COL2A1 protein, human
  • Collagen Type II
  • Cyclin-Dependent Kinase Inhibitor p21
  • High Mobility Group Proteins
  • RNA, Messenger
  • SOX9 Transcription Factor
  • SOX9 protein, human
  • STAT Transcription Factors
  • Transcription Factors
  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3
  • Mitogen-Activated Protein Kinases