Synovectomy reduces stromal-cell-derived factor-1 (SDF-1) which is involved in the destruction of cartilage in osteoarthritis and rheumatoid arthritis

被引:95
作者
Kanbe, K [1 ]
Takemura, T [1 ]
Takeuchi, K [1 ]
Chen, Q [1 ]
Takagishi, K [1 ]
Inoue, K [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Orthopaed Surg, Arakawa Ku, Tokyo 1168567, Japan
来源
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME | 2004年 / 86B卷 / 02期
关键词
D O I
10.1302/0301-620X.86B2.14474
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
We have compared the concentrations of stromal-cell-derived factor-1 (SDF-1), matrix metalloproteinase-1 (MMP-1), MMP-9 and MMP-13 in serum before and after synovectomy or total knee replacement (TKR). We confirmed the presence of SDF-1 and its receptor CXCR4 in the synovium and articular cartilage by immunohistochemistry. We established chondrocytes by using mutant CXCR4 to block the release of MMPs. The level of SDF-1 was decreased 5.1- and 6.7-fold in the serum of patients with OA and RA respectively, after synovectomy compared with that before surgery. MMP-9 and MMP-13 were decreased in patients with OA and RA after synovectomy. We detected SDF-1 in the synovium and the bone marrow but not in cartilage. CXCR4 was detected in articular cartilage. SDF-1 increased the release of MMP-9 and MMP-13 from chondrocytes in a dose-dependent manner. The mutant CXCR4 blocked the release of MMP-9 and MMP-13 from chondrocytes by retrovirus vector. Synovectomy is effective in patients with OA or RA because SDF-1, which can regulate the release of MMP-9 and MMP-13 from articular chondrocytes for breakdown of cartilage, is removed by the operation.
引用
收藏
页码:296 / 300
页数:5
相关论文
共 21 条
[1]   DIAGNOSTIC AND THERAPEUTIC USES OF THE ARTHROSCOPE IN RHEUMATOID-ARTHRITIS AND OSTEOARTHRITIS [J].
ALTMAN, RD ;
GRAY, R .
AMERICAN JOURNAL OF MEDICINE, 1983, 75 (4B) :50-55
[2]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]   Stromal cell-derived factor 1 (CXCL12) induces monocyte migration into human synovium transplanted onto SCID mice [J].
Blades, MC ;
Ingegnoli, F ;
Wheller, SK ;
Manzo, A ;
Wahid, S ;
Panayi, GS ;
Perretti, M ;
Pitzalis, C .
ARTHRITIS AND RHEUMATISM, 2002, 46 (03) :824-836
[4]   Arthroscopic synovectomy of the elbow in rheumatoid arthritis [J].
Horiuchi, K ;
Momohara, S ;
Tomatsu, T ;
Inoue, K ;
Toyama, Y .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2002, 84A (03) :342-347
[5]  
Kalela A, 2000, EUR J CLIN INVEST, V30, P99
[6]  
Kanbe K, 2002, ARTHRITIS RHEUM-US, V46, P130, DOI 10.1002/1529-0131(200201)46:1<130::AID-ART10020>3.0.CO
[7]  
2-D
[8]   A CXC chemokine receptor, CXCR5/BLR1, is a novel and specific coreceptor for human immunodeficiency virus type 2 [J].
Kanbe, K ;
Shimizu, N ;
Soda, Y ;
Takagishi, K ;
Hoshino, H .
VIROLOGY, 1999, 265 (02) :264-273
[9]  
Katschke KJ, 2001, ARTHRITIS RHEUM, V44, P1022, DOI 10.1002/1529-0131(200105)44:5<1022::AID-ANR181>3.0.CO
[10]  
2-N