Department of Oral Biology, Medical University of Vienna, 1090 Vienna, Austria.
Department of Periodontology, School of Dental Medicine, University of Bern, 3010 Bern, Switzerland.
Int J Mol Sci. 2020 Oct 15;21(20):7629. doi: 10.3390/ijms21207629.
Solid platelet-rich fibrin (PRF) is produced with centrifugation tubes designed to accelerate clotting. Thus, activated platelets may accumulate within the fibrin-rich extracellular matrix even before centrifugation is initiated. It can thus be assumed that platelets and their growth factors such as transforming growth factor-β (TGF-β) are trapped within PRF independent of their relative centrifugal force (RCF), the gravitation or -force. To test this assumption, we prepared PRF membranes with tubes where clotting is activated by a silicone-coated interior. Tubes underwent 210 , 650 and 1500 for 12 min in a horizontal centrifuge. The respective PRF membranes, either in total or separated into a platelet-poor plasma and buffy coat fraction, were subjected to repeated freeze-thawing to prepare lysates. Gingival fibroblasts were exposed to the PRF lysates to provoke the expression of TGF-β target genes. We show here that the expression of interleukin 11 (IL11) and NADPH oxidase 4 (NOX4), and Smad2/3 signaling were similarly activated by all lysates when normalized to the size of the PRF membranes. Notably, platelet-poor plasma had significantly less TGF-β activity than the buffy coat fraction at both high-speed protocols. In contrast to our original assumption, the TGF-β activity in PRF lysates produced using horizontal centrifugation follows a gradient with increasing concentration from the platelet-poor plasma towards the buffy coat layer.
固体富血小板纤维蛋白 (PRF) 是通过设计用于加速凝血的离心管产生的。因此,激活的血小板甚至在开始离心之前就可能在富含纤维蛋白的细胞外基质中积聚。因此,可以假设血小板及其生长因子(如转化生长因子-β(TGF-β))被困在 PRF 中,而不受其相对离心力(RCF)、重力或力的影响。为了验证这一假设,我们使用内部涂有硅酮的管来激活凝血来制备 PRF 膜。管在水平离心机中以 210 、650 和 1500 分别进行 12 分钟。将相应的 PRF 膜(全部或分为血小板贫乏血浆和白细胞层)进行反复冻融以制备裂解物。牙龈成纤维细胞暴露于 PRF 裂解物中以引发 TGF-β 靶基因的表达。我们在这里表明,当标准化到 PRF 膜的大小时,所有裂解物都以类似的方式激活白细胞介素 11 (IL11) 和 NADPH 氧化酶 4 (NOX4) 和 Smad2/3 信号。值得注意的是,在两种高速方案中,血小板贫乏血浆的 TGF-β 活性明显低于白细胞层。与我们最初的假设相反,使用水平离心产生的 PRF 裂解物中的 TGF-β 活性遵循从血小板贫乏血浆向白细胞层逐渐增加的浓度梯度。