Reactive oxygen species induce expression of vascular endothelial growth factor in chondrocytes and human articular cartilage explants 英文参考文献.docVIP
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Reactive oxygen species induce expression of vascular endothelial growth factor in chondrocytes and human articular cartilage explants 英文参考文献
Available online /content/8/6/R189
Research article
Open Access
Vol 8 No 6
Reactive oxygen species induce expression of vascular
endothelial growth factor in chondrocytes and human articular
cartilage explants
Jakob Fay1, Deike Varoga2, Christoph J Wruck2, Bodo Kurz2, Mary B Goldring3,4 and
Thomas Pufe2
1Department of Trauma Surgery, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller-Strasse 7, 24105 Kiel, Germany
2Department of Anatomy, Christian-Albrechts-University Kiel, Olshausenstrasse 40, 24098 Kiel, Germany
3Beth Israel Deaconess Medical Center, New England Baptist Bone and Joint Institute, Harvard Institutes of Medicine, HIM-246, 4 Blackfan Circle,
Boston, MA 02115-5713, USA
4Hospital for Special Surgery, Caspary Research Building, Room 528, 535 E. 70th Street, New York, NY 10021, USA
Corresponding author: Thomas Pufe, t.pufe@anat.uni-kiel.de
Received: 13 Oct 2006 Revisions requested: 9 Nov 2006 Revisions received: 1 Dec 2006 Accepted: 23 Dec 2006 Published: 23 Dec 2006
Arthritis Research Therapy 2006, 8:R189 (doi:10.1186/ar2102)
This article is online at: /content/8/6/R189
? 2006 Fay et al.; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Vascular endothelial growth factor (VEGF) promotes cartilage-
degrading pathways, and there is evidence for the involvement
of reactive oxygen species (ROS) in cartilage degeneration.
However, a relationship between ROS and VEGF has not been
reported. Here, we investigate whether the expression of VEGF
is modulated by ROS.
PCR. Expression of VEGF and VEGF receptors (VEGFR-1 and
VEGFR-2) was quantified by real-time RT-PCR.
Synovial fluid from OA patients revealed markedly elevated levels
of VEGF. Common RT-PCR revealed that the splice variants
were
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