Tumor necrosis factor α-induced adipose-related protein expression in experimental arthritis and in rheumatoid arthritis 英文参考文献.docVIP
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Tumor necrosis factor α-induced adipose-related protein expression in experimental arthritis and in rheumatoid arthritis 英文参考文献
Available online /content/11/4/R118
Research article
Open Access
Vol 11 No 4
Tumor necrosis factor α-induced adipose-related protein
expression in experimental arthritis and in rheumatoid arthritis
Asuka Inoue1, Isao Matsumoto1,2, Yoko Tanaka1, Keiichi Iwanami1, Akihiro Kanamori3,
Naoyuki Ochiai3, Daisuke Goto1, Satoshi Ito1 and Takayuki Sumida1
1Division of Clinical Immunology, Advanced Biomedical Applications, Graduate School of Comprehensive Human Sciences, University of Tsukuba,
1-1-1 Tennodai, Tsukuba 305-8575, Japan
2PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho Kawaguchi, Saitama 332-0012, Japan
3Department of Orthopedic Surgery, Advanced Biomedical Applications, Graduate School of Comprehensive Human Sciences, University of
Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8575, Japan
Corresponding author: Isao Matsumoto, ismatsu@md.tsukuba.ac.jp
Received: 6 Feb 2009 Revisions requested: 11 Mar 2009 Revisions received: 1 Aug 2009 Accepted: 6 Aug 2009 Published: 6 Aug 2009
Arthritis Research Therapy 2009, 11:R118 (doi:10.1186/ar2779)
This article is online at: /content/11/4/R118
? 2009 Inoue 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
Introduction Tumor necrosis factor-alpha (TNFα) plays a pivotal
Results Among the arrayed TNFα-related genes, the expression
of TIARP mRNA was the highest (more than 20 times the
control). TIARP mRNA was detected specifically in joints and
spleens of arthritic mice, and their levels in the synovia
correlated with severity of joint swelling. Treatment with anti-
TNF mAb significantly reduced TIARP mRNA expression in
splenocytes. Among the splenocytes, CD11b+ cells were the
main source of TIARP mRNA. Immunohistochemistry showed
that
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