Department of Periodontology, Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam and Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
J Periodontal Res. 2023 Jun;58(3):483-492. doi: 10.1111/jre.13116. Epub 2023 Mar 21.
To investigate the effect of Advanced Platelet-Rich Fibrin (A-PRF+), Leukocyte Platelet-Rich Fibrin (L-PRF), and injectable Platelet-Rich Fibrin (i-PRF) on osteogenesis of a human osteoblast-like cell line in vitro.
Different PRF protocols are used in clinical dentistry in the last years. Recent literature documented the positive impact of PRF derivatives in vivo and in vitro, on different types of cells. However, hardly any literature comparing the new protocols for PRF (the A-PRF+ and i-PRF) with the original protocol of PRF (L-PRF) is present for osteoblast-like cells.
A-PRF+, L-PRF, and i-PRF were prepared from six male donors and pre-cultured with 10 mL culture medium for 6 days. 5 x 10 cells/ml osteoblasts from the osteoblast cell line (U2OS) were seeded and cultured either with conditioned medium derived from the different PRF conditions or with regular culture medium. At five different time points (0, 7, 14, 21, 28 days), the osteogenic capacity of the cells was assessed with Alizarin Red S to visualize mineralization. Also in these cells, the calcium concentration and alkaline phosphatase activity were investigated. Using qPCR, the expression of alkaline phosphatase, osteocalcin, osteonectin, ICAM-1, RUNX-2, and collagen 1a was assessed.
In osteoblast-like cells cultured with conditioned medium, the A-PRF+ conditioned medium induced more mineralization and calcium production after 28 days of culturing compared with the control (p < .05). No significant differences were found in the extent of cell proliferation between the different conditions. RUNX-2 and osteonectin mRNA expression in the cells were lower in all PRF-stimulated cultures compared with control at different time points. The i-PRF-conditioned medium induced more ALP activity (p < .05) compared with control and osteoblasts-like cells differentiated more compared with osteoblasts cultured with L-PRF.
The three PRF preparations seem to have the capacity to increase the osteogenic potential of osteoblast-like cells. A-PRF+ seems to have the highest potential for mineralization, while i-PRF seems to have the potential to enhance early cell differentiation.
研究富血小板纤维蛋白(A-PRF+)、白细胞富血小板纤维蛋白(L-PRF)和可注射富血小板纤维蛋白(i-PRF)对体外人成骨样细胞系成骨的影响。
近年来,不同的 PRF 方案在临床牙科中得到了应用。最近的文献记录了 PRF 衍生物在体内和体外对不同类型细胞的积极影响。然而,几乎没有任何文献比较新的 PRF 方案(A-PRF+和 i-PRF)与原始的 PRF 方案(L-PRF)对成骨样细胞的影响。
从 6 名男性供体中制备 A-PRF+、L-PRF 和 i-PRF,并预培养 6 天,用 10 ml 培养基培养。将 5x10 个/ml 的成骨细胞系(U2OS)成骨细胞接种并培养在不同 PRF 条件下的条件培养基或常规培养基中。在 0、7、14、21 和 28 天的 5 个不同时间点,用茜素红 S 评估细胞的成骨能力以显示矿化。还在这些细胞中研究了钙浓度和碱性磷酸酶活性。使用 qPCR 评估碱性磷酸酶、骨钙素、骨粘连蛋白、ICAM-1、RUNX-2 和胶原 1a 的表达。
在与条件培养基培养的成骨样细胞中,与对照组相比,A-PRF+条件培养基在培养 28 天后诱导更多的矿化和钙产生(p<.05)。在不同条件下,细胞增殖的程度没有差异。在不同时间点,所有 PRF 刺激培养物中的 RUNX-2 和骨粘连蛋白 mRNA 表达均低于对照组。与对照组相比,i-PRF 条件培养基诱导更高的碱性磷酸酶活性(p<.05),与 L-PRF 培养的成骨样细胞相比,i-PRF 培养的成骨样细胞分化更多。
三种 PRF 制剂似乎都有增加成骨样细胞成骨潜能的能力。A-PRF+似乎具有最高的矿化潜力,而 i-PRF 似乎具有增强早期细胞分化的潜力。