Tissue inhibitor of metalloproteinases 4 (TIMP4) is involved in inflammatory processes of human cardiovascular pathology

被引:70
作者
Koskivirta, Ilpo
Rahkonen, Otto
Mayranpaa, Mikko
Pakkanen, Sari
Husheem, Michael
Sainio, Annele
Hakovirta, Harri
Laine, Jukka
Jokinen, Eero
Vuorio, Eero
Kovanen, Petri
Jarvelainen, Hannu
机构
[1] Univ Turku, Cent Hosp, Dept Med, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Med Biochem & Mol Biol, FIN-20520 Turku, Finland
[3] Univ Turku, Dept Anat, FIN-20520 Turku, Finland
[4] Univ Turku, Dept Surg, FIN-20520 Turku, Finland
[5] Univ Turku, Dept Pathol, FIN-20520 Turku, Finland
[6] Univ Helsinki, Dept Pediat, FIN-00014 Helsinki, Finland
[7] Wihuri Res Inst, SF-00140 Helsinki, Finland
关键词
TIMP4; inflammation; atherosclerosis; giant cell arteritis; heart allograft rejection;
D O I
10.1007/s00418-006-0163-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tissue inhibitors of matrix metalloproteinases (TIMPs) comprise a family of four members, of which TIMP4 is characterized by being primarily restricted to cardiovascular structures. We demonstrate with immunohistochemical analysis of healthy human tissue that TIMP4 is present in medial smooth muscle cells and adventitial capillaries of arteries as well as in cardiomyocytes. Animal studies have suggested a role for TIMP4 in several inflammatory diseases and cardiovascular pathologies. We therefore examined whether TIMP4 is involved in human inflammatory cardiovascular disorders, specifically atherosclerosis, giant cell arteritis and chronic rejection of heart allografts. TIMP4 was most clearly visible in cardiovascular tissue areas populated by abundant inflammatory cells, mainly macrophages and CD3+ T cells. Using western blotting and immunocytochemistry, human blood derived lymphocytes, monocytes/macrophages and mast cells were shown to produce TIMP4. In advanced atherosclerotic lesions, TIMP4 was detected around necrotic lipid cores, whereas TIMP3 and caspase 3 resided within and around the core regions, indicating different roles for TIMP3 and TIMP4 in inflammation-induced apoptosis and in matrix turnover. In conclusion, the data demonstrate upregulation of TIMP4 in human cardiovascular disorders exhibiting inflammation, suggesting its future use as a novel systemic marker for vascular inflammation.
引用
收藏
页码:335 / 342
页数:8
相关论文
共 36 条
[1]   Uniaxial strain upregulates matrix-degrading enzymes produced by human vascular smooth muscle cells [J].
Asanuma, K ;
Magid, R ;
Johnson, C ;
Nerem, RM ;
Galis, ZS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 284 (05) :H1778-H1784
[2]   Metalloproteinase inhibitors: biological actions and therapeutic opportunities [J].
Baker, AH ;
Edwards, DR ;
Murphy, G .
JOURNAL OF CELL SCIENCE, 2002, 115 (19) :3719-3727
[3]   Analyses of all matrix metalloproteinase members in leukocytes emphasize monocytes as major inflammatory mediators in multiple sclerosis [J].
Bar-Or, A ;
Nuttall, RK ;
Duddy, M ;
Alter, A ;
Kim, HJ ;
Ifergan, I ;
Pennington, CJ ;
Bourgoin, P ;
Edwards, DR ;
Yong, VW .
BRAIN, 2003, 126 :2738-2749
[4]   Inhibition of adjuvant-induced arthritis by systemic tissue inhibitor of metalloproteinases 4 gene delivery [J].
Çeliker, MY ;
Ramamurthy, N ;
Xu, JW ;
Wang, MS ;
Jiang, YF ;
Greenwald, R ;
Shi, YE .
ARTHRITIS AND RHEUMATISM, 2002, 46 (12) :3361-3368
[5]   Inhibition of Wilms' tumor growth by intramuscular administration of tissue inhibitor of metalloproteinases-4 plasmid DNA [J].
Çeliker, MY ;
Wang, M ;
Atsidaftos, E ;
Liu, X ;
Liu, YE ;
Jiang, Y ;
Valderrama, E ;
Goldberg, ID ;
Shi, YE .
ONCOGENE, 2001, 20 (32) :4337-4343
[6]   Expression of matrix metalloproteinase-26 and tissue inhibitor of matrix metalloproteinase-3 and-4 in endometrium throughout the normal menstrual cycle and alteration in users of levonorgestrel implants who experience irregular uterine bleeding [J].
Chegini, N ;
Rhoton-Vlasak, A ;
Williams, RS .
FERTILITY AND STERILITY, 2003, 80 (03) :564-570
[7]   Gene expression profiling of peripheral blood mononuclear cells from cattle infected with Mycobacterium paratuberculosis [J].
Coussens, PM ;
Colvin, CJ ;
Wiersma, K ;
Abouzied, A ;
Sipkovsky, S .
INFECTION AND IMMUNITY, 2002, 70 (10) :5494-5502
[8]   TIMP-4 is regulated by vascular injury in rats [J].
Dollery, CM ;
McEwan, JR ;
Wang, MS ;
Sang, QXA ;
Liu, YLE ;
Shi, YE .
CIRCULATION RESEARCH, 1999, 84 (05) :498-504
[9]  
Green MA, 1996, PROG PHOTOVOLTAICS, V4, P375, DOI 10.1002/(SICI)1099-159X(199609/10)4:5<375::AID-PIP146>3.0.CO
[10]  
2-S