A novel anti-platelet peptide (Z4A5) potential for glycoprotein IIb/IIIa inhibits platelet aggregation |
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Authors: | Li Ying-Xue Sun Qiang Zhang Hui Ren Shu-Ting Liao Yi-Ran Wang Ya Shen Xin-Liang Wang Bing |
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Institution: | a School of Medicine, Xi'an Jiaotong University, Xi'an Shaanxi, Chinab Therapeutic Vaccines Research Center, Shaanxi, Chinac China National Biotec Group, Beijing, China |
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Abstract: | IntroductionZ4A5 is a novel peptide that inhibits platelet aggregation and formation of platelet thrombi, but the mechanism of its anti-platelet effects remains unknown. This study explores the anti-platelet effect and mechanism of Z4A5.MethodsWe investigated the anti-platelet activity of Z4A5 on platelet aggregation induced by adenosine diphosphate (ADP), arachidonic acid (AA) and thrombin (TH) in human platelet-rich plasma (PRP). Fibrinogen and PAC-1 binding to glycoproteinIIb/IIIa (GPIIb/IIIa) were measured by flow cytometry. In addition, we investigated the integrin specificity of Z4A5 in attachment and detachment assays using human umbilical vein endothelial cells (HUVEC) and assessed the relative cell number using the MTT assay.ResultsIn vitro, Z4A5 inhibited ADP-, AA- and TH-induced human platelet aggregation with IC50 values of 0.46 ± 0.05 μM (n = 10), 0.23 ± 0.05 μM (n = 10) and 0.21 ± 0.02 μM (n = 10), respectively. Z4A5 inhibited fibrinogen, and PAC-1 bound to platelet GPIIb/IIIa with IC50 values of 0.48 ± 0.07 μM (n = 8) and 0.63 ± 0.12 μM (n = 6), respectively. Z4A5 failed to inhibit αVβ3 integrin-mediated HUVEC attachment to vitronectin and did not cause any significant detachment of HUVEC monolayer when compared with the controls.ConclusionsZ4A5 is a potential anti-platelet drug that inhibits fibrinogen binding to GPIIb/IIIa, but does not affect the structurally similar integrin αVβ3. |
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Keywords: | flow cytometry glycoproteinIIb/IIIa integrin specificity platelet aggregation Z4A5 |
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