Journal of Molecular Medicine

, Volume 80, Issue 4, pp 258–266

The Ets 1 transcription factor is upregulated during inflammatory angiogenesis in rheumatoid arthritis

Authors

  • Nicolas Wernert
    • Institute of Pathology, University of Bonn, P.O. Box 2120, 53011 Bonn
  • Hans-Peter Justen
    • Clinic of Orthopedics, University of Regensburg, Bavarian Red Cross Hospital for Rheumatic Diseases, Bad Abbach
  • Marcus Rothe
    • Institute of Pathology, University of Bonn, P.O. Box 2120, 53011 Bonn
  • Peter Behrens
    • Institute of Pathology, University of Bonn, P.O. Box 2120, 53011 Bonn
  • Stephan Dreschers
    • Institute of Pathology, University of Bonn, P.O. Box 2120, 53011 Bonn
  • Thomas Neuhaus
    • Medizinische Poliklinik, University of Bonn, Wilhelmstrasse 35-37, 53111 Bonn
  • Alexandra Florin
    • Institute of Pathology, University of Bonn, P.O. Box 2120, 53011 Bonn
  • Agapios Sachinidis
    • Medizinische Poliklinik, University of Bonn, Wilhelmstrasse 35-37, 53111 Bonn
  • Hans Vetter
    • Medizinische Poliklinik, University of Bonn, Wilhelmstrasse 35-37, 53111 Bonn
  • Yon Ko
    • Medizinische Poliklinik, University of Bonn, Wilhelmstrasse 35-37, 53111 Bonn
Original Article

DOI: 10.1007/s00109-001-0316-0

Cite this article as:
Wernert, N., Justen, H., Rothe, M. et al. J Mol Med (2002) 80: 258. doi:10.1007/s00109-001-0316-0

Abstract

Neovascularization of the inflamed synovium and pannus is one of the hallmarks of chronic rheumatoid arthritis. It contributes to disease progression by supplying blood to the inflamed tissues and by recruiting immune competent and inflammatory cells. Angiogenesis is tightly regulated at several levels, but of significant importance is transcription. The Ets 1 transcription factor has been intimately linked to the regulation of angiogenesis under both physiological and pathological conditions and is induced in endothelial cells by vascular endothelial growth factor, the most important angiogenic factor in rheumatoid arthritis. We investigated Ets 1 expression in synovial membranes of joints in patients with active rheumatoid arthritis and compared the results to those obtained in patients with degenerative joint disease, which is characterized by significantly less neoangiogenesis. Using quantitative densitometric and real-time RT-PCR approaches, we found a significant upregulation of Ets 1 transcripts in rheumatic, compared to osteoarthritic, synovial membranes. Moreover, we were able to attribute both Ets 1 mRNA and Ets 1 protein to capillary endothelial cells of newly formed blood vessels by in situ hybridization and immunohistochemistry. Finally, our data suggest important roles of the Ets 1 transcription factor in the regulation of inflammatory angiogenesis in rheumatoid arthritis.

Ets 1 Arthritis Real-time PCR In situ hybridization Immunohistochemistry
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Copyright information

© Springer-Verlag 2002