Demonstration of mast cell chemotactic activity in synovial fluid from rheumatoid patients

被引:41
作者
Olsson, N
Ulfgren, AK
Nilsson, G [1 ]
机构
[1] Uppsala Univ, Dept Genet & Pathol, Rudbeck Lab, S-75185 Uppsala, Sweden
[2] Karolinska Hosp, Rheumatol Unit, Dept Med, S-10401 Stockholm, Sweden
关键词
D O I
10.1136/ard.60.3.187
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives-The significance of the mast cell in the pathogenesis of rheumatic diseases has become more evident. Although mast cell hyperplasia is a feature of rheumatoid arthritis, the nature of mast cell chemoattractants involved in the recruitment of mast cells in joint diseases has not been studied in any detail. In this study the presence of mast cell chemotactic activity in synovial fluids was examined. Methods-Synovial fluids from seven rheumatoid patients were tested in a modified Boyden chamber, where a human mast cell line was used as responder. The presence of stem cell factor (SCF) and transforming growth factor beta (TGF beta) was measured by enzyme linked immunosorbent assay (ELISA). Results-Six of the seven synovial fluids tested exhibited mast cell chemotactic activity. Two characterised human mast cell chemotaxins, SCF and TGF beta, were highly expressed in the synovium. Soluble SCF could be detected in all fluids analysed. Blocking antibodies against SCF or TGF beta almost completely blocked the activity in one fluid, partially blocked the activity in three, and did not affect the activity in two. Treatment of the responder cells with pertussis toxin reduced the migratory response against seven fluids, indicating the presence of chemoattractants mediating their effect through G(i) coupled receptors. Conclusion-These data demonstrate the presence of multiple factors in synovial fluid acting as mast cell chemoattractants, two of which are SCF and TGF beta that contribute to the effect. These findings may be of importance for developing new strategies to inhibit mast cell accumulation in rheumatic diseases.
引用
收藏
页码:187 / 193
页数:7
相关论文
共 50 条
[1]   RAPID ONSET SYNOVIAL INFLAMMATION AND HYPERPLASIA INDUCED BY TRANSFORMING GROWTH FACTOR-BETA [J].
ALLEN, JB ;
MANTHEY, CL ;
HAND, AR ;
OHURA, K ;
ELLINGSWORTH, L ;
WAHL, SM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (01) :231-247
[2]   The chemoattractant activity of rheumatoid synovial fluid for human lymphocytes is due to multiple cytokines [J].
AlMughales, J ;
Blyth, TH ;
Hunter, JA ;
Wilkinson, PC .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1996, 106 (02) :230-236
[3]  
ARNETT FC, 1987, ARTHRITIS RHEUM, V31, P315
[4]   Mast cell activation in arthritis: detection of alpha- and beta-tryptase, histamine and eosinophil cationic protein in synovial fluid [J].
Buckley, MG ;
Walters, C ;
Wong, WM ;
Cawley, MID ;
Ren, S ;
Schwartz, LB ;
Walls, AF .
CLINICAL SCIENCE, 1997, 93 (04) :363-370
[5]   ESTABLISHMENT OF AN IMMATURE MAST-CELL LINE FROM A PATIENT WITH MAST-CELL LEUKEMIA [J].
BUTTERFIELD, JH ;
WEILER, D ;
DEWALD, G ;
GLEICH, GJ .
LEUKEMIA RESEARCH, 1988, 12 (04) :345-355
[6]   THE MICROSCOPIC STRUCTURE OF NORMAL HUMAN SYNOVIAL TISSUE [J].
CASTOR, CW .
ARTHRITIS AND RHEUMATISM, 1960, 3 (02) :140-151
[7]  
Ceponis A, 1998, J RHEUMATOL, V25, P2304
[8]   ARTICULAR MASTOCYTOSIS IN RHEUMATOID-ARTHRITIS [J].
CRISP, AJ ;
CHAPMAN, CM ;
KIRKHAM, SE ;
SCHILLER, AL ;
KRANE, SM .
ARTHRITIS AND RHEUMATISM, 1984, 27 (08) :845-851
[9]   Quantitative analysis of synovial membrane inflammation: a comparison between automated and conventional microscopic measurements [J].
Cunnane, G ;
Bjork, L ;
Ulfgren, AK ;
Lindblad, S ;
FitzGerald, O ;
Bresnihan, B ;
Andersson, U .
ANNALS OF THE RHEUMATIC DISEASES, 1999, 58 (08) :493-499
[10]  
DEVOS S, 1993, CANCER RES, V53, P3638