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首页> 外文期刊>Clinical oral implants research >Modulation of platelet activation and initial cytokine release by alloplastic bone substitute materials.
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Modulation of platelet activation and initial cytokine release by alloplastic bone substitute materials.

机译:异体骨替代材料对血小板活化和初始细胞因子释放的调节。

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OBJECTIVES: Platelet-derived cytokines play a crucial role in tissue regeneration. In regenerative dental medicine, bone substitute materials (BSM) are widely used. However, initial interactions of BSM and platelets are still unknown. The aim of this study was to evaluate the potential of platelet activation and subsequent initial cytokine release by different commercial alloplastic BSM. MATERIAL AND METHODS: Eight commercial BSM of different origins and chemical compositions (tricalcium phosphate, hydroxyapatite, bioactive glass: SiO(2) and mixtures) were incubated with a platelet concentrate (platelet-rich plasma, PRP) of three healthy volunteers at room temperature for 15 min. Platelet count, aggregation, degranulation (activated surface receptor CD62p) and cytokine release (Platelet-derived growth factor, Vascular endothelial growth factor) into the supernatant were quantified. Highly thrombogenic collagen served as a reference. RESULTS: The investigated PRP samples revealed different activation patterns when incubated with different BSM. In general, SiO(2)-containing BSM resulted in high platelet activation and cytokine release. In detail, pure bioactive glass promoted platelet activation most significantly, followed by hybrid BSM containing lower ratios of SiO(2). Additionally, we found indications of cytokine retention by BSM of large specific surfaces. CONCLUSIONS: Platelet activation as well as consecutive storage and slow release of platelet-derived cytokines are desirable attributes of modern BSM. Within the limits of the study, SiO(2)-containing BSM were identified as promising biomaterials. Further investigations on cytokine adsorption and cytokine release kinetics by the respective BSM have to be conducted.
机译:目的:血小板源性细胞因子在组织再生中起关键作用。在再生牙科医学中,广泛使用骨替代材料(BSM)。但是,BSM和血小板的初始相互作用仍然未知。这项研究的目的是评估通过不同的商业同种异体BSM血小板活化和随后初始细胞因子释放的潜力。材料与方法:将八种不同来源和化学成分的商业BSM(磷酸三钙,羟基磷灰石,生物活性玻璃:SiO(2)和混合物)与三名健康志愿者的血小板浓缩液(富血小板血浆,PRP)一起在室温下孵育15分钟量化上清液中的血小板计数,聚集,脱颗粒(活化的表面受体CD62p)和细胞因子释放(血小板衍生的生长因子,血管内皮生长因子)。高度血栓形成的胶原蛋白作为参考。结果:研究的PRP样品在与不同的BSM孵育时显示出不同的激活模式。通常,包含SiO(2)的BSM导致高血小板活化和细胞因子释放。详细地说,纯生物活性玻璃最显着地促进了血小板活化,其次是含有较低比例SiO(2)的混合BSM。此外,我们发现了大比表面的BSM可以保留细胞因子。结论:血小板活化以及血小板源性细胞因子的连续储存和缓慢释放是现代BSM的理想属性。在研究的范围内,含SiO(2)的BSM被确定为有前途的生物材料。必须对各个BSM进行的细胞因子吸附和细胞因子释放动力学的进一步研究。

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