Expression of ADAM15 in rheumatoid synovium up-regulation by vascular endothelial growth factor and possible implications for angiogenesis.docVIP
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Expression of ADAM15 in rheumatoid synovium up-regulation by vascular endothelial growth factor and possible implications for angiogenesis
Available online /content/7/6/R1158
Research article
Open Access
Vol 7 No 6
Expression of ADAM15 in rheumatoid synovium: up-regulation by
vascular endothelial growth factor and possible implications for
angiogenesis
Koichiro Komiya1,2, Hiroyuki Enomoto2, Isao Inoki1, Satoko Okazaki1, Yoshinari Fujita1,2, Eiji Ikeda1,
Eiko Ohuchi3, Hideo Matsumoto2, Yoshiaki Toyama2 and Yasunori Okada1
1Department of Pathology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, Japan
2Department of Orthopaedic Surgery, School of Medicine, Keio University, Shinjuku-ku, Tokyo, Japan
3Biopharmaceutical Department, Daiichi Fine Chemical Co. Ltd., Takaoka, Toyama, Japan
Corresponding author: Yasunori Okada, okada@sc.itc.keio.ac.jp
Received: 28 May 2005 Revisions requested: 20 Jun 2005 Revisions received: 23 Jun 2005 Accepted: 27 Jun 2005 Published: 5 Aug 2005
Arthritis Research Therapy 2005, 7:R1158-R1173 (DOI 10.1186/ar1796)
This article is online at: /content/7/6/R1158
? 2005 Komiya 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
ADAMs (a disintegrin and metalloproteinases) comprise a new
gene family of metalloproteinases, and may play roles in cell-cell
interaction, cell migration, signal transduction, shedding of
membrane-anchored proteins and degradation of extracellular
matrix. We screened the mRNA expression of 10 different
ADAMs with a putative metalloproteinase motif in synovial
expression levels and vascular density in the synovial tissues (r
= 0.907, p 0.001; n = 20). ADAM15 was constitutively
expressed in RA synovial fibroblasts and human umbilical vein
endothelial cells (HUVECs), and the expression level was
increased in HUVECs by treatment with vascular endothelial
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