Volume 3 Supplement 1

Innovative Rheumatology: Gene and Cell Therapies of Arthritis and Related Autoimmune Disorders. Second International Meeting

Open Access

A member of the T-box family of transcription factors mediates cartilage formation in mesenchymal progenitors C3H10T1/2

  • A Hoffmann1,
  • S Czichos1,
  • C Kaps1,
  • D Bächner1,
  • H Mayer1,
  • BG Kurkalli2,
  • Y Zilberman2,
  • D Gazit2 and
  • G Gross1
Arthritis Research & Therapy20013(Suppl 1):P29

DOI: 10.1186/ar355

Received: 6 April 2001

Published: 25 April 2001

The bone morphogenetic protein 2 (BMP2)-dependent onset of osteo-/chondrogenic differentiation in the acknowledged pluripotent murine mesenchymal progenitor cell line C3H10T1/2 is accompanied by the immediate upregulation of fibroblast growth factor receptor3 (FGFR3) and by a delayed upregulation of FGFR2. This direct FGFR3-mediated expression seems to be essential for the onset of chondrogenesis since the forced expression of activated FGFR3 is sufficient for differentiation into the chondrogenic lineage. The screening for FGFR3-regulated transcription factors exhibiting a chondrogenic capacity in C3H10T1/2 indentified a T-box containing transcription factor. Forced expression of this factor is sufficient for the initiation of chondrogenic differentiationin mesenchymal progenitors C3H10T1/2 in vitro. Implantation of these recombinant progenitors at ectopic intramuscular sites of the mouse was followed by massive cartilage formation substantiating the chondrogenic potential of this transcription factor. A potential role for this T-box factor in chondrogenesis is also suggested by its expression in various skeletal elements at late stages of murine embryonic development as demonstrated by in situ hybridization. These studies indicate that BMP2 triggers onset of FGFR3-dependent signaling in mesenchymal progenitors C3H10T1/2 to induce a novel type of transcription factor for the initiation of chondrogenic differentiation.

Authors’ Affiliations

(1)
Osteogenesis Group, Gesellschaft für Biotechnologische Forschung (GBF)
(2)
Molecular Pathology, Hebrew University

Copyright

© BioMed Central Ltd 2001

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