Pepelassi Eudoxie A, Markopoulou Cleopatra E, Dereka Xanthippi E, Mamalis Anastasios A, Vrotsos Ioannis A, Koutsilieris Michael
Department of Periodontology, School of Dentistry, University of Athens, Greece.
J Int Acad Periodontol. 2009 Jan;11(1):160-8.
The purpose of this study was to evaluate the gingival fibroblast proliferative response derived from patients with chronic and aggressive periodontitis to homologous platelet-rich plasma (PRP).
Gingival fibroblasts derived from nine patients with chronic periodontitis, aggressive periodontitis and healthy periodontium were grown. Medium was replaced with DMEM containing 0.5% FBS in which cells remained for two days. Cells were incubated and cultured with medium containing 50 microl/ml homologous platelet-rich plasma (PRP) or not containing PRP (control) for 24 and 48 hours. PRP originated from three donors. Cell proliferation effect was evaluated at 24 and 48 hours. Cell viability was assessed with a hemocytometer. Viable cells were counted under a phase contrast microscope.
The results revealed that incubation of human gingival fibroblasts, derived from healthy and intact periodontium, chronic periodontitis and aggressive periodontitis, in culture medium containing homologous PRP statistically significantly increased the cell proliferation at 24 and 48 hours of culture.
The addition of PRP to human gingival fibroblast cultures significantly increased the proliferative response, irrespective of the presence of periodontitis, type of periodontitis and PRP donor.
本研究旨在评估慢性和侵袭性牙周炎患者的牙龈成纤维细胞对同源富血小板血浆(PRP)的增殖反应。
培养来自9例慢性牙周炎、侵袭性牙周炎患者及健康牙周组织患者的牙龈成纤维细胞。培养基更换为含0.5%胎牛血清的DMEM,细胞在其中培养两天。细胞分别与含50微升/毫升同源富血小板血浆(PRP)或不含PRP(对照)的培养基孵育并培养24小时和48小时。PRP来自三名供体。在24小时和48小时评估细胞增殖效应。用血细胞计数器评估细胞活力。在相差显微镜下对活细胞进行计数。
结果显示,将来自健康完整牙周组织、慢性牙周炎和侵袭性牙周炎的人牙龈成纤维细胞在含同源PRP的培养基中培养,在培养24小时和48小时时,细胞增殖在统计学上显著增加。
向人牙龈成纤维细胞培养物中添加PRP可显著增加增殖反应,无论是否存在牙周炎、牙周炎类型及PRP供体如何。