IgG deposition and activation of the classical complement pathway involvement in the activation of human granulocytes by decellularized porcine heart valve tissue

被引:36
作者
Bastian, Fabienne [1 ,3 ]
Stelzmueller, Marie-Elisabeth [1 ]
Kratochwill, Klaus [2 ]
Kasimir, Marie-Theres [1 ]
Simon, Paul [1 ]
Weigel, Guenter [1 ,3 ]
机构
[1] Med Univ Vienna, Dept Cardiothorac Surg, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Pediat & Adolescent Med, RCU Pediat Biochem & Analyt, A-1090 Vienna, Austria
[3] Ludwig Boltzmann Cluster Cardiovasc Res, Vienna, Austria
关键词
complement; extracellular matrix; inflammation; leukocytes; heart valve;
D O I
10.1016/j.biomaterials.2008.01.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Decellularization treatment of heart valves has been thought to eliminate tissue immunogenicity. Early failure of tissue-engineered xenogeneic heart valves was seen in children and has been a major drawback in this promising field of research. This study was designed to characterize the effects of acellular porcine heart valve tissue on immune activation in vitro. Incubation of decellularized porcine tissue with human plasma led to adsorption of IgG, activation of the classical complement pathway and adhesion of activated polymorphonuclear leukocytes (PMN). This inflammatory response was strongly inhibited by proteins extracted from native porcine tissue which might indicate that inhibitors of PMN activation present in the extracellular matrix (ECM) are lost during the decellularization process. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1824 / 1832
页数:9
相关论文
共 22 条
[1]   Xenogeneic extracellular matrix as a scaffold for tissue reconstruction [J].
Badylak, SF .
TRANSPLANT IMMUNOLOGY, 2004, 12 (3-4) :367-377
[2]   RAPID METHOD FOR THE ISOLATION OF NEUTROPHILS IN HIGH-YIELD WITHOUT THE USE OF DEXTRAN OR DENSITY GRADIENT POLYMERS [J].
EGGLETON, P ;
GARGAN, R ;
FISHER, D .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 121 (01) :105-113
[3]  
Gemmell CH, 1996, J BIOMED MATER RES, V32, P29, DOI 10.1002/(SICI)1097-4636(199609)32:1<29::AID-JBM4>3.0.CO
[4]  
2-R
[5]   Complement inhibition reduces material-induced leukocyte activation with PEG modified polystyrene beads (Tentagel™) but not polystyrene beads [J].
Gorbet, MB ;
Sefton, MV .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2005, 74A (04) :511-522
[6]   Biomaterial-associated thrombosis: roles of coagulation factors, complement, platelets and leukocytes [J].
Gorbet, MB ;
Sefton, MV .
BIOMATERIALS, 2004, 25 (26) :5681-5703
[7]   Interactions of the extracellular matrix proteoglycans decorin and biglycan with C1q and collectins [J].
Groeneveld, TWL ;
Oroszlán, M ;
Owens, RT ;
Faber-Krol, MC ;
Bakker, AC ;
Arlaud, GJ ;
McQuillan, DJ ;
Kishore, U ;
Daha, MR ;
Roos, A .
JOURNAL OF IMMUNOLOGY, 2005, 175 (07) :4715-4723
[8]   Decellularized heart valve as a scaffold for in vivo recellularization: Deleterious effects of granulocyte colony-stimulating factor [J].
Juthier, F ;
Vincentelli, A ;
Gaudric, J ;
Corseaux, D ;
Fouquet, O ;
Calet, C ;
Le Tourneau, T ;
Soenen, V ;
Zawadzki, C ;
Fabre, O ;
Susen, S ;
Prat, A ;
Jude, B .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2006, 131 (04) :843-852
[9]  
Lhotta K, 1998, KIDNEY INT, V53, P1044
[10]   Deposition of C3b/iC3b leads to the concealment of antigens, immunoglobulins and bound C1q in complement-activating immune complexes [J].
Nilsson, UR .
MOLECULAR IMMUNOLOGY, 2001, 38 (2-3) :151-160