Antiphospholipid Antibodies Affect Human Endometrial Angiogenesis: Protective Effect of a Synthetic Peptide (TIFI) Mimicking the Phospholipid Binding Site of β2glycoprotein I

被引:45
作者
Di Simone, Nicoletta [1 ]
D'Ippolito, Silvia [1 ]
Marana, Riccardo [1 ,2 ]
Di Nicuolo, Fiorella [1 ]
Castellani, Roberta [1 ]
Pierangeli, Silvia S. [3 ]
Chen, Pojen [4 ]
Tersigni, Chiara [1 ]
Scambia, Giovanni [1 ]
Meroni, Pier Luigi [5 ]
机构
[1] Univ Cattolica Sacro Cuore, Dept Obstet & Gynecol, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Int Sci Inst, Paolo VI Inst, Rome, Italy
[3] Univ Texas Med Branch, Dept Internal Med, Galveston, TX 77555 USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
[5] Univ Milan, Ist Auxol Italiano, Inst G Pini, Div Rheumatol, I-20122 Milan, Italy
关键词
Antiphospholipid antibodies; endometrial angiogenesis; TIFL; ENDOTHELIAL GROWTH-FACTOR; FETAL LOSS; ANTI-BETA-2-GLYCOPROTEIN-I ANTIBODIES; PATHOGENIC MECHANISM; TROPHOBLAST CELLS; FACTOR EXPRESSION; ACTIVATION; THROMBOSIS; MATRIX-METALLOPROTEINASE-9; MIGRATION;
D O I
10.1111/aji.12130
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Problem Aim of our study was to investigate whether TIFI, a syntetic peptide able to compete with anti-phospholipid antibodies (aPL) in the binding to endothelium, may restore aPL-inhibited endometrial angiogenesis. Methods The protective role of TIFI was evaluated on: i) aPL-inhibited of human endometrial endothelial cells (HEEC) angiogenesis in vitro; ii) aPL-inhibited vascular endothelial growth factor (VEGF) and metalloproteases (MMPs) expression; iii) aPL-inhibited Nuclear Factor-kappa B (NF-kappa B) and Extracellular signal-Regulated Kinase (ERK) activation and (iv) angiogenesis in vivo. Results TIFI restores in a dose-dependent manner: i) aPL-mediated inhibition of HEEC angiogenesis in vitro and in vivo (P < 0.05), ii) VEGF (P < 0.001) and MMP-2 (P < 0.05) expression and iii) NF-kappa B DNA binding and ERK-1/2 activation (P < 0.05) inhibited by aPL. Conclusion Our results show for the first time the protective effects of TIFI, as represented by its ability to interfere with aPL mediated anti-angiogenic activity.
引用
收藏
页码:299 / 308
页数:10
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