IFN-γ pretreatment augments immune complex-induced matrix metalloproteinase-1 expression in U937 histiocytes

被引:8
作者
Anderson, F
Game, BA
Atchley, D
Xu, MF
Lopes-Virella, MF
Huang, Y
机构
[1] Med Univ S Carolina, Dept Med, Ralph H Johnson Vet Adm Med Ctr, Charleston, SC 29403 USA
[2] Med Univ S Carolina, Dept Med, Div Endocrinol Diabet & Med Genet, Charleston, SC 29403 USA
关键词
IFN-gamma; LDL; metalloproteinase; immune complex;
D O I
10.1006/clim.2001.5161
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We reported recently that immune complexes (ICs) induced matrix metalloproteinase-1 (AMP-1) expression in U937 histiocytes. The present study was undertaken to determine the effect of pretreatment of U937 cells with interferon-gamma (IFN-gamma) on IC-induced MMP-1 expression. Our flow cytometry studies showed that IFN-gamma upregulated the surface expression of FcgammaRI, but not FcgammaRII. Results also showed that pretreatment of the cells with IFN-gamma augmented LDL-containing IC (LDL-10-induced NRKP-1 secretion in a dose- and time-dependent manner. Furthermore, Northern blot analysis revealed that IFN-gamma pretreatment led to a marked increase in MMP-1 mRNA. Finally, we demonstrated that PD98059 was able to block LDL-IC-induced MMP-1 secretion, regardless of whether the cells were pretreated with IFN-gamma or not, suggesting that IFN-gamma pretreatment did not alter the essential role of the ERR signaling pathway in LDL-IC-induced MMP-1 expression. In conclusion, the present study has demonstrated that IFN-gamma pretreatment augments LDL-IC-induced AMP-1 expression in U937 cells, thus elucidating an immune mechanism potentially involved in plaque destabilization. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:200 / 207
页数:8
相关论文
共 35 条
[1]   CYTOKINES AND GROWTH-FACTORS POSITIVELY AND NEGATIVELY REGULATE INTERSTITIAL COLLAGEN GENE-EXPRESSION IN HUMAN VASCULAR SMOOTH-MUSCLE CELLS [J].
AMENTO, EP ;
EHSANI, N ;
PALMER, H ;
LIBBY, P .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (05) :1223-1230
[2]   Enhanced levels of soluble and membrane-bound CD40 ligand in patients with unstable angina -: Possible reflection of T lymphocyte and platelet involvement in the pathogenesis of acute coronary syndromes [J].
Aukrust, P ;
Müller, F ;
Ueland, T ;
Berget, T ;
Aaser, E ;
Brunsvig, A ;
Solum, NO ;
Forfang, K ;
Froland, SS ;
Gullestad, L .
CIRCULATION, 1999, 100 (06) :614-620
[3]   Cellular responses to interferon-gamma [J].
Boehm, U ;
Klamp, T ;
Groot, M ;
Howard, JC .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :749-795
[4]   Fc receptor biology [J].
Daeron, M .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :203-234
[5]  
DURDEN DL, 1995, J IMMUNOL, V154, P4039
[6]  
DURDEN DL, 1994, BLOOD, V84, P2102
[7]   INCREASED EXPRESSION OF MATRIX METALLOPROTEINASES AND MATRIX-DEGRADING ACTIVITY IN VULNERABLE REGIONS OF HUMAN ATHEROSCLEROTIC PLAQUES [J].
GALIS, ZS ;
SUKHOVA, GK ;
LARK, MW ;
LIBBY, P .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2493-2503
[8]   ULTRASTRUCTURAL STUDIES ON THE LOCALIZATION OF IGG IN THE AORTIC ENDOTHELIUM AND SUB-ENDOTHELIAL INTIMA OF ATHEROSCLEROTIC AND NON-ATHEROSCLEROTIC RABBITS [J].
HANSSON, GK ;
BONDJERS, G ;
BYLOCK, A ;
HJALMARSSON, L .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 1980, 33 (03) :302-315
[9]   LOCALIZATION OF LYMPHOCYTES-T AND MACROPHAGES IN FIBROUS AND COMPLICATED HUMAN ATHEROSCLEROTIC PLAQUES [J].
HANSSON, GK ;
JONASSON, L ;
LOJSTHED, B ;
STEMME, S ;
KOCHER, O ;
GABBIANI, G .
ATHEROSCLEROSIS, 1988, 72 (2-3) :135-141
[10]   IMMUNE-MECHANISMS IN ATHEROSCLEROSIS [J].
HANSSON, GK ;
JONASSON, L ;
SEIFERT, PS ;
STEMME, S .
ARTERIOSCLEROSIS, 1989, 9 (05) :567-578