Antiphospholipid antibodies affect human endometrial angiogenesis: protective effect of a synthetic peptide (TIFI) mimicking the phospholipid binding site of β(2) glycoprotein I

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. The protective role of TIFI was evaluated on: i) aPL-inhibited of human endometrial endothel...

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Veröffentlicht in:American journal of reproductive immunology (1989) 2013-10, Vol.70 (4), p.299-308
Hauptverfasser: Di Simone, Nicoletta, D'Ippolito, Silvia, Marana, Riccardo, Di Nicuolo, Fiorella, Castellani, Roberta, Pierangeli, Silvia S, Chen, Pojen, Tersigni, Chiara, Scambia, Giovanni, Meroni, Pier Luigi
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Sprache:eng
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Zusammenfassung: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. 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-κB (NF-κB) and Extracellular signal-Regulated Kinase (ERK) activation and (iv) angiogenesis in vivo. 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-κB DNA binding and ERK-1/2 activation (P < 0.05) inhibited by aPL. 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.
ISSN:1600-0897
DOI:10.1111/aji.12130